Search Clinical Trials
Sponsor Condition of Interest |
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Bladder Fiducial Markers and Multiparametric-MRI (mp-MRI) to Optimize Bladder Chemo-radiotherapy
Cedars-Sinai Medical Center
Bladder Cancer
Urinary Bladder Neoplasm
Urologic Neoplasms
Neoplasms
Urinary Bladder Diseases
The purpose of this study is to examine the usefulness of implanting small 24-K gold
fiducial markers around a bladder tumor site, so that a Radiation Oncologist can identify
the original tumor location at the time of radiation treatment. Other goals of the study
include assessing whether a new MRI1 expand
The purpose of this study is to examine the usefulness of implanting small 24-K gold fiducial markers around a bladder tumor site, so that a Radiation Oncologist can identify the original tumor location at the time of radiation treatment. Other goals of the study include assessing whether a new MRI imaging technology can help with detection of bladder cancer earlier and more accurately when evidence of bladder cancer is not visible by scope. Type: Interventional Start Date: Jul 2020 |
MitraClip REPAIR MR Study
Abbott Medical Devices
Mitral Valve Regurgitation
The objective of this randomized controlled trial (RCT) is to compare the clinical
outcome of MitraClip™ device versus surgical repair in patients with severe primary MR
who are at moderate surgical risk and whose mitral valve has been determined to be
suitable for correction by MV repair surgery b1 expand
The objective of this randomized controlled trial (RCT) is to compare the clinical outcome of MitraClip™ device versus surgical repair in patients with severe primary MR who are at moderate surgical risk and whose mitral valve has been determined to be suitable for correction by MV repair surgery by the cardiac surgeon on the local site heart team. Type: Interventional Start Date: Jul 2020 |
Ziftomenib Maintenance Post Allo-HCT
Massachusetts General Hospital
Acute Myeloid Leukemia
Acute Myeloid Leukemia in Remission
NPM1 Mutation
KMT2A Rearrangement
The purpose of this study is to test the safety, effects, and recommended dose of an
investigational drug, ziftomenib, in addition to the standard treatment on blood cancer
with Allogeneic Hematopoietic Cell Transplantation (allo-HCT). This study plans to learn
more about ziftomenib, which targets1 expand
The purpose of this study is to test the safety, effects, and recommended dose of an investigational drug, ziftomenib, in addition to the standard treatment on blood cancer with Allogeneic Hematopoietic Cell Transplantation (allo-HCT). This study plans to learn more about ziftomenib, which targets and inhibits negative interactions within cancer cells related to AML, when given after allo-HCT, to determine if it improves outcomes following allo-HCT. The name of the study drug involved in this study is: • Ziftomenib Type: Interventional Start Date: Jun 2024 |
Epilepsy Learning Healthcare System (ELHS)
Epilepsy Foundation of America
Epilepsy
Seizure Disorder
Neurologic Disorder
Rare Diseases
The Epilepsy Learning Health System (ELHS) is a quality improvement and research network
to improve outcomes for people with epilepsy. The ELHS is designed as a model of
value-based chronic care for epilepsy as envisioned by the National Academies of Medicine
Committee in their landmark reports "Th1 expand
The Epilepsy Learning Health System (ELHS) is a quality improvement and research network to improve outcomes for people with epilepsy. The ELHS is designed as a model of value-based chronic care for epilepsy as envisioned by the National Academies of Medicine Committee in their landmark reports "The Learning Health System" and "Epilepsy Across the Spectrum: Promoting Health and Understanding". The ELHS network is a collaboration among clinicians, patients and researchers that promotes the use of data for multiple purposes including one-on-one clinical care, population management, quality improvement and research. The ELHS Registry includes data on children and adults with epilepsy collected during the process of standard epilepsy care. These data are used to create population health reports and to track changes in outcomes over time. ELHS teams use quality improvement methods, such as Plan-Do-Study-Act (PDSA) cycles, to continuously learn how to improve care. Type: Observational [Patient Registry] Start Date: Mar 2019 |
Trajectories of Recovery After Intravenous Propofol Versus Inhaled VolatilE Anesthesia Trial
Washington University School of Medicine
Surgery-Complications
Anesthesia Complication
Anesthesia Awareness
Anesthesia
Surgery
The investigators will conduct a 12,500-patient randomized multi-center trial to
determine (i) which general anesthesia technique yields superior patient recovery
experiences in any of three surgical categories ((a) major inpatient surgery, (b) minor
inpatient surgery, (c) outpatient surgery) and (1 expand
The investigators will conduct a 12,500-patient randomized multi-center trial to determine (i) which general anesthesia technique yields superior patient recovery experiences in any of three surgical categories ((a) major inpatient surgery, (b) minor inpatient surgery, (c) outpatient surgery) and (ii) whether TIVA confers no more than a small (0.2 %) increased risk of intraoperative awareness than INVA in patients undergoing both outpatient and inpatient surgeries Type: Interventional Start Date: Sep 2023 |
Intermuscular Coherence as a Biomarker for ALS
University of Chicago
Amyotrophic Lateral Sclerosis
The specific aims of this study are to:
1. Determine if a painless and quick measurement of muscle activity using surface
electrodes can help with the diagnosis of ALS. Specifically, we ask if a measure of
intermuscular coherence (IMC-βγ), when added to current diagnostic criteria (Awa1 expand
The specific aims of this study are to: 1. Determine if a painless and quick measurement of muscle activity using surface electrodes can help with the diagnosis of ALS. Specifically, we ask if a measure of intermuscular coherence (IMC-βγ), when added to current diagnostic criteria (Awaji criteria), can differentiate ALS from mimic diseases more accurately and earlier than currently possible. 2. Characterize IMC-βγ in neurotypical subjects by age, sex, race, and ethnicity. 3. Follow a cohort of ALS patients longitudinally to determine if IMC-βγ changes with ALS disease progression and whether such changes correlate with functional and clinical scores, or survival. Type: Observational Start Date: Mar 2021 |
Atezolizumab+Bevacizumab+SBRT in Unresectable HCC
Massachusetts General Hospital
Unresectable Hepatocellular Carcinoma
This research study is evaluating the safety and tolerability of the drugs atezolizumab
and bevacizumab with stereotactic body radiation therapy (SBRT) for treating unresectable
hepatocellular carcinoma.
This study involves the following interventions:
- Atezolizumab
- Bevacizumab
- St1 expand
This research study is evaluating the safety and tolerability of the drugs atezolizumab and bevacizumab with stereotactic body radiation therapy (SBRT) for treating unresectable hepatocellular carcinoma. This study involves the following interventions: - Atezolizumab - Bevacizumab - Stereotactic body radiation therapy (SBRT) Type: Interventional Start Date: Aug 2022 |
Developing Fast Pediatric Imaging
Boston Children's Hospital
Pediatric Low-grade Gliomas
This research study is evaluating the investigational software for magnetic resonance
imaging (MRI) systems and techniques to process magnetic resonance (MR) images expand
This research study is evaluating the investigational software for magnetic resonance imaging (MRI) systems and techniques to process magnetic resonance (MR) images Type: Interventional Start Date: Apr 2019 |
Open Pilot Trial of a Mind-body Program for Cardiac Arrest Survivors and Their Caregivers
Massachusetts General Hospital
Emotional Distress
Cardiac Arrest
The purpose of this study is to pilot a mind-body intervention for cardiac arrest
survivors and their informal caregivers, Recovering Together after Cardiac Arrest. The
data the investigators gather in this study will be used to further refine our
intervention. expand
The purpose of this study is to pilot a mind-body intervention for cardiac arrest survivors and their informal caregivers, Recovering Together after Cardiac Arrest. The data the investigators gather in this study will be used to further refine our intervention. Type: Interventional Start Date: Aug 2024 |
Telehealth and Onsite Maintenance Exercise in Chronic Lung Disease
MGH Institute of Health Professions
Copd
COPD Exacerbation
COPD Bronchitis
Emphysema or COPD
Chronic Lung Disease
The goal of this pilot clinical trial is to compare telehealth and onsite supervised
maintenance exercise program for adults with Chronic Lung Disease.
The specific aims of the study are:
- To compare 8-week supervised maintenance program delivered onsite and via tele-rehab
with no mainte1 expand
The goal of this pilot clinical trial is to compare telehealth and onsite supervised maintenance exercise program for adults with Chronic Lung Disease. The specific aims of the study are: - To compare 8-week supervised maintenance program delivered onsite and via tele-rehab with no maintenance for patients with Chronic Lung Disease following discharge from traditional exercise or physical therapy or onsite outpatient rehabilitation programs on clinical outcomes (dyspnea, exercise capacity, physical function, physical activity, and quality of life) at 8 weeks and 4-months post-intervention. - To compare the differences in dyspnea, exercise capacity, physical function, physical activity, and quality of life between an 8-week maintenance program delivered onsite and via tele-rehab at 8-weeks and 4-months post-intervention in patients with Chronic Lung Disease following discharge from traditional onsite outpatient rehabilitation. Participants in both intervention groups (onsite and tele-rehab) will undergo a baseline onsite assessment followed by an 8-week supervised exercise intervention either onsite or in a telehealth setting. Control group will receive biweekly check in calls, but no active intervention. Type: Interventional Start Date: Sep 2023 |
Cerebrospinal Fluid Biomarkers of Myotonic Dystrophy
Massachusetts General Hospital
Myotonic Dystrophy Type 1
Myotonic dystrophy is associated with central sleep apnea, excessive daytime sleepiness,
diminished working memory, impaired visuospatial skills, and deficits in problem-solving
skills.
Cerebrospinal fluid (CSF) is a clear, colorless fluid that surrounds and protects the
brain.
Changes in the com1 expand
Myotonic dystrophy is associated with central sleep apnea, excessive daytime sleepiness, diminished working memory, impaired visuospatial skills, and deficits in problem-solving skills. Cerebrospinal fluid (CSF) is a clear, colorless fluid that surrounds and protects the brain. Changes in the composition of CSF can serve as early indicators of changes in brain activity and function. The purpose of this research is to learn about myotonic dystrophy by examining cerebrospinal fluid and brain activity in participants. The tests will be low risk and are well tolerated. The information that we gather from this study may help us evaluate, prevent, diagnose, treat, and improve our understanding of myotonic dystrophy. Funding Source- FDA OOPD Type: Observational Start Date: Aug 2022 |
Study of Iadademstat and Gilteritinib in Patients With R/R AML With FMS-like Tyrosine Kinase Mutati1
Oryzon Genomics S.A.
Acute Myeloid Leukemia, in Relapse
Acute Myeloid Leukemia Refractory
Iadademstat is being studied as a treatment for subjects with Relapsed or Refractory
Acute Myeloid Leukemia (R/R AML) with FMS-like tyrosine kinase mutation (FLT3 mut+).
During the trial, iadademstat will be given in combination with gilteritinib, a drug that
is already approved to treat patients w1 expand
Iadademstat is being studied as a treatment for subjects with Relapsed or Refractory Acute Myeloid Leukemia (R/R AML) with FMS-like tyrosine kinase mutation (FLT3 mut+). During the trial, iadademstat will be given in combination with gilteritinib, a drug that is already approved to treat patients with FLT3-mutated R/R AML. Type: Interventional Start Date: Nov 2022 |
A Phase I/II Study of DYP688 in Patients With Metastatic Uveal Melanoma and Other GNAQ/11 Mutant Me1
Novartis Pharmaceuticals
Metastatic Uveal Melanoma
This is a FIH, phase I/II, open label, multi-center study of DYP688 as a single agent.
The purpose of this study is to characterize the safety, tolerability, and anti-tumor
activity of DYP688 as a single agent in patients with metastatic uveal melanoma (MUM) and
other melanomas harboring GNAQ/11 mu1 expand
This is a FIH, phase I/II, open label, multi-center study of DYP688 as a single agent. The purpose of this study is to characterize the safety, tolerability, and anti-tumor activity of DYP688 as a single agent in patients with metastatic uveal melanoma (MUM) and other melanomas harboring GNAQ/11 mutations. Type: Interventional Start Date: Jul 2022 |
Estrogen Administration for the Treatment of NASH in Postmenopausal Women
Massachusetts General Hospital
NASH - Nonalcoholic Steatohepatitis
Non-alcoholic fatty liver disease (NAFLD) is a growing epidemic in the United States.
Despite this, the treatment options remain limited. Preclinical and preliminary clinical
data suggest that estrogen deficiency plays an important role in the pathology of
steatosis, inflammation and fibrosis in no1 expand
Non-alcoholic fatty liver disease (NAFLD) is a growing epidemic in the United States. Despite this, the treatment options remain limited. Preclinical and preliminary clinical data suggest that estrogen deficiency plays an important role in the pathology of steatosis, inflammation and fibrosis in non-alcoholic steatohepatitis (NASH), the progressive form of NAFLD. Post-menopausal women are a growing population with particularly high risk of NASH due to their lack of estrogen. This study will examine the effect of estradiol on hepatic fibrosis and fat in post-menopausal women with NASH. Type: Interventional Start Date: Dec 2021 |
Study to Evaluate Safety, Tolerability, and Optimal Dose of Candidate GBM Vaccine VBI-1901 in Recur1
VBI Vaccines Inc.
Glioblastoma Multiforme
The purpose of this study is to assess the safety and tolerability of VBI-1901 in
subjects with recurrent malignant gliomas (glioblastoma, or GBM). expand
The purpose of this study is to assess the safety and tolerability of VBI-1901 in subjects with recurrent malignant gliomas (glioblastoma, or GBM). Type: Interventional Start Date: Dec 2017 |
Permissive Hypotension After Cardiac Surgery
Massachusetts General Hospital
Surgery
The objective of this pilot randomized controlled trial is to demonstrate the feasibility
of implementing a pragmatic clinical trial randomizing patients to permissive hypotension
versus usual care and to determine the impact of permissive hypotension on vasopressor
exposure, ICU length of stay, ma1 expand
The objective of this pilot randomized controlled trial is to demonstrate the feasibility of implementing a pragmatic clinical trial randomizing patients to permissive hypotension versus usual care and to determine the impact of permissive hypotension on vasopressor exposure, ICU length of stay, markers of end organ perfusion, and clinically relevant patient outcomes. The data collected from this pilot study will be used as preliminary data for study design and grant applications for a larger multicenter randomized controlled trial. Type: Interventional Start Date: Apr 2024 |
Neuroactive Steroid to Treat Depressed Mood: A Trial for People With HIV
Massachusetts General Hospital
Major Depressive Disorder
Anxiety Depression
HIV
This study will determine the effects of pregnenolone on brain function, inflammation and
depressive symptoms in people with HIV who have depression. Participants in this study
will receive a pill of either pregnenolone or placebo, and can stay on their current
antidepression medications. Brain ima1 expand
This study will determine the effects of pregnenolone on brain function, inflammation and depressive symptoms in people with HIV who have depression. Participants in this study will receive a pill of either pregnenolone or placebo, and can stay on their current antidepression medications. Brain imaging and behavioral assessments will be performed during the study. Type: Interventional Start Date: Mar 2023 |
Computational Neuroscience of Language Processing in the Human Brain
Massachusetts General Hospital
Language
Epilepsy
Language is a signature human cognitive skill, but the precise computations that support
language understanding remain unknown. This study aims to combine high-quality human
neural data obtained through intracranial recordings with advances in computational
modeling of human cognition to shed light1 expand
Language is a signature human cognitive skill, but the precise computations that support language understanding remain unknown. This study aims to combine high-quality human neural data obtained through intracranial recordings with advances in computational modeling of human cognition to shed light on the construction and understanding of speech. Type: Interventional Start Date: Apr 2021 |
FOLFIRINOX + 9-Ing-41 + Losartan In Pancreatic Cancer
Colin D. Weekes, M.D., PhD
Pancreatic Adenocarcinoma
Pancreatic Adenocarcinoma Metastatic
The purpose of this study is to find out if an experimental drug will prevent metastatic
pancreatic adenocarcinoma from becoming resistant to standard treatment for the disease.
The names of the study drugs involved in this study are:
- 9-ING-41
- Losartan
- Ferumoxytol
- FOLFIRINO1 expand
The purpose of this study is to find out if an experimental drug will prevent metastatic pancreatic adenocarcinoma from becoming resistant to standard treatment for the disease. The names of the study drugs involved in this study are: - 9-ING-41 - Losartan - Ferumoxytol - FOLFIRINOX (made up of 4 different drugs): - 5-Fluorouracil (5-FU) - Oxaliplatin - Irinotecan - Leucovorin Type: Interventional Start Date: Mar 2022 |
Polygenic Risk-based Detection of Subclinical Coronary Atherosclerosis and Intervention With Statin1
Massachusetts General Hospital
Coronary Artery Disease
The goal of this double-blind randomized controlled trial is to determine how treatment
with high intensity statin, low-dose colchicine, and their combination modulates
progression and composition of coronary atherosclerosis in individuals with high
polygenic risk for coronary artery disease. expand
The goal of this double-blind randomized controlled trial is to determine how treatment with high intensity statin, low-dose colchicine, and their combination modulates progression and composition of coronary atherosclerosis in individuals with high polygenic risk for coronary artery disease. Type: Interventional Start Date: Dec 2023 |
Defining the Role of Palliative carE for Patients With Hematologic Malignancies Undergoing Adoptive1
Massachusetts General Hospital
Hematologic Malignancy
Blood Cancer
Lymphoma
Leukemia
Multiple Myeloma
The goal of this study is to determine whether a palliative care intervention (PEACE) can
improve the quality of life and experiences of participants with Lymphoma, Leukemia, or
Multiple Myeloma receiving adoptive cellular therapy (ACT). After completion of an open
pilot, participants will be rando1 expand
The goal of this study is to determine whether a palliative care intervention (PEACE) can improve the quality of life and experiences of participants with Lymphoma, Leukemia, or Multiple Myeloma receiving adoptive cellular therapy (ACT). After completion of an open pilot, participants will be randomly assigned into one of two study intervention groups. The names of the study intervention groups involved in this study are: - Palliative care (PEACE) plus usual oncology care - Usual care (standard oncology care) Participation in this research study is expected to last for up to 2 years. It is expected that about 90 people will take part in this research study. Type: Interventional Start Date: Dec 2022 |
Use of Ketosis in Modulating Metabolic Pathways in Bipolar Disorder
Stony Brook University
Bipolar Disorder
Bipolar Disorder Type 1
The goal of this clinical trial is to test how specific components of diet affect brain
function and behavior for individuals with bipolar. The main question it aims to answer
is how glucose and ketones each affect the brain's response to risk and reward.
Participants will be asked to provide blood1 expand
The goal of this clinical trial is to test how specific components of diet affect brain function and behavior for individuals with bipolar. The main question it aims to answer is how glucose and ketones each affect the brain's response to risk and reward. Participants will be asked to provide blood (to assess baseline measures of how the body uses energy), and then to receive two MRI scan sessions, on separate days. During each MRI scan session, participants will play three games, from which they can win money, before and after drinking glucose (on one day) or ketones (on the other day). Investigators will compare individuals with and without bipolar to test whether the two groups differ in how their brains use energy, and to test how the brain's use of energy affects behavior. Type: Interventional Start Date: Jan 2024 |
Positive Emotions Following Acute Cardiac Events
Massachusetts General Hospital
Acute Coronary Syndrome
Physical Inactivity
The focus of this study is to test the efficacy of a 12-week, remotely delivered,
positive-psychology-motivational interviewing (PP-MI) intervention, with additional twice
weekly text messages for a total of 24 weeks (with interactive, algorithm-driven,
goal-focused text messages in the final 12 we1 expand
The focus of this study is to test the efficacy of a 12-week, remotely delivered, positive-psychology-motivational interviewing (PP-MI) intervention, with additional twice weekly text messages for a total of 24 weeks (with interactive, algorithm-driven, goal-focused text messages in the final 12 weeks), compared to post-acute coronary syndrome (ACS) treatment as usual, in a randomized trial of 280 post-ACS patients with low baseline physical activity. Type: Interventional Start Date: Sep 2022 |
Study of Anitocabtagene-autoleucel in Relapsed or Refractory Multiple Myeloma (iMMagine-1)
Kite, A Gilead Company
Multiple Myeloma
A Phase II study of anitocabtagene-autoleucel (formerly CART-ddBCMA) for patients with
relapsed or refractory multiple myeloma. Anitocabtagene-autoleucel is a BCMA-directed
CAR-T cell therapy. expand
A Phase II study of anitocabtagene-autoleucel (formerly CART-ddBCMA) for patients with relapsed or refractory multiple myeloma. Anitocabtagene-autoleucel is a BCMA-directed CAR-T cell therapy. Type: Interventional Start Date: Aug 2022 |
ViTAA Registry Pre- and Post-Operative Monitoring for Endovascular Aortic Aneurysm Repair and Seria1
ViTAA Medical Solutions
Abdominal Aortic Aneurysms
This is a Prospective Registry study to collect imaging and clinical data both on
patients with aortic aneurysm disease undergoing serial monitoring and on patients pre
and post-endovascular repair, using ViTAA (The Sponsor) aortic mapping technology. expand
This is a Prospective Registry study to collect imaging and clinical data both on patients with aortic aneurysm disease undergoing serial monitoring and on patients pre and post-endovascular repair, using ViTAA (The Sponsor) aortic mapping technology. Type: Observational [Patient Registry] Start Date: Dec 2021 |
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