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US National OCS Heart Perfusion (OHP) Registry
TransMedics
Heart Transplant
This Registry is a sponsor initiated, multi-center, observational post-approval registry
with independent academic oversight. expand
This Registry is a sponsor initiated, multi-center, observational post-approval registry with independent academic oversight. Type: Observational [Patient Registry] Start Date: Aug 2023 |
Cannabis and Opioid Use Disorder
University of Kentucky
Opioid Use Disorder
This study plans to enroll participants with opioid use disorder who are not currently
seeking treatment to assess the effects of cannabis on opioid withdrawal and other
related outcomes. expand
This study plans to enroll participants with opioid use disorder who are not currently seeking treatment to assess the effects of cannabis on opioid withdrawal and other related outcomes. Type: Interventional Start Date: Sep 2024 |
Effect of Music on Cardiopulmonary Exercise Capacity in Heart Failure Patients
Maya Ignaszewski
Heart Failure
The study aims to assess the effect of music on the heart resulting in a change in their
exercise capacity among systolic heart failure patients undergoing Cardiopulmonary
Exercise testing. expand
The study aims to assess the effect of music on the heart resulting in a change in their exercise capacity among systolic heart failure patients undergoing Cardiopulmonary Exercise testing. Type: Interventional Start Date: Sep 2022 |
Biopsy Collection and Repository Database
Andrew Kolodziej
Cardiovascular Diseases
Use samples procured from patients to improve understanding of molecular, cellular, and
tissue-level processes produced by a variety of cardiac diseases and therapeutic
interventions. expand
Use samples procured from patients to improve understanding of molecular, cellular, and tissue-level processes produced by a variety of cardiac diseases and therapeutic interventions. Type: Observational Start Date: Dec 2021 |
GENOCARE: a Prospective, Randomized Clinical Trial of Genotype-Guided Dosing Versus Usual Care
Reema A. Patel
Colorectal Cancer
Pancreatic Cancer
This is a prospective, randomized study designed to compare genotype-guided dosing to
usual care in patients with pancreas cancer and colorectal cancer who are UGT1A1
intermediate metabolizers (*1/*28) (heterozygotes) and usual UGT metabolizers (*1/*1).
All patients will be assessed for UGT1A1 geno1 expand
This is a prospective, randomized study designed to compare genotype-guided dosing to usual care in patients with pancreas cancer and colorectal cancer who are UGT1A1 intermediate metabolizers (*1/*28) (heterozygotes) and usual UGT metabolizers (*1/*1). All patients will be assessed for UGT1A1 genotype at screening and those with intermediate or usual UGT1A1 genotypes (*1/*28, *1/*1) will be randomized to genotype-guided dosing versus usual care. Type: Interventional Start Date: Sep 2022 |
Melanoma Margins Trial-II: 1cm v 2cm Wide Surgical Excision Margins for AJCC Stage II Primary Cutan1
Melanoma and Skin Cancer Trials Limited
Cutaneous Melanoma, Stage II
Patients with a primary invasive melanoma are recommended to undergo excision of the
primary lesion with a wide margin. There is evidence that less radical margins of
excision may be just as safe. This is a randomised controlled trial of 1 cm versus 2 cm
margin of excision of the primary lesion for1 expand
Patients with a primary invasive melanoma are recommended to undergo excision of the primary lesion with a wide margin. There is evidence that less radical margins of excision may be just as safe. This is a randomised controlled trial of 1 cm versus 2 cm margin of excision of the primary lesion for adult patients with stage II primary invasive cutaneous melanomas (AJCC 8th edition) to determine differences in disease-free survival. A reduction in margins is expected to improve patient quality of life. Type: Interventional Start Date: Dec 2019 |
Auditory Biofeedback Gait Training Individuals With Chronic Ankle Instability
University of Kentucky
Ankle Sprains
Ankle Injuries and Disorders
The goal of this randomized clinical controlled trial is examine the effects of gait
training with auditory biofeedback (AudFB) on gait biomechanics, clinical measures of
ankle joint health, and patient-centered outcomes. The following specific aims will
achieve this objective:
- Specific Aim 11 expand
The goal of this randomized clinical controlled trial is examine the effects of gait training with auditory biofeedback (AudFB) on gait biomechanics, clinical measures of ankle joint health, and patient-centered outcomes. The following specific aims will achieve this objective: - Specific Aim 1: Determine if a 6-week gait training with AudFB intervention improves lower extremity biomechanics compared to a Control condition in participants with CAI. - Specific Aim 2: Determine if a 6-week gait training with AudFB reduces talar cartilage deformation compared to a Control condition in participants with CAI. - Specific Aim 3: Determine if a 6-week gait training with AudFB reduces episodes of ankle giving-way and reduces self-perceived severity of symptoms relative to a Control condition in participants with CAI. Participants will: - Complete 12 intervention sessions over a 6-week period of walking, ruck marching, and runninig. - Complete testing sessions before and after the intervention, then after 6 and 12-months following the intervention. Type: Interventional Start Date: May 2025 |
Exercise and Emotional Learning in Posttraumatic Stress Disorder
Christal L Badour
PTSD
The goal of this clinical trial is to test how exercise affects learning and memory
processes relevant to the treatment of PTSD. Participants will complete a baseline intake
followed by two experimental sessions. During the first experimental session,
participants will undergo an MRI session of ima1 expand
The goal of this clinical trial is to test how exercise affects learning and memory processes relevant to the treatment of PTSD. Participants will complete a baseline intake followed by two experimental sessions. During the first experimental session, participants will undergo an MRI session of imaginal exposure to traumatic memory cues followed by 30-minutes of moderate intensity exercise or low intensity exercise. Participants will complete a second session of imaginal exposure with MRI 24 hours later. Type: Interventional Start Date: May 2024 |
Precision Medicine Randomized Clinical Trial Comparing Molecular Tumor Board Assisted Care to Usual1
Timothy Mullett
Non-Small Cell Lung Cancer
This trial will compare Molecular Tumor Board (MTB) assisted care to usual care for
patients who have newly diagnosed histologically or cytologically confirmed stage IIb-IV
Non-Small Cell Lung Cancer (NSCLC) and are planning to undergo treatment for their
cancer. expand
This trial will compare Molecular Tumor Board (MTB) assisted care to usual care for patients who have newly diagnosed histologically or cytologically confirmed stage IIb-IV Non-Small Cell Lung Cancer (NSCLC) and are planning to undergo treatment for their cancer. Type: Interventional Start Date: Apr 2022 |
CRISPR-Edited Allogeneic Anti-BCMA CAR-T Cell Therapy in Patients With Relapsed/Refractory Multiple1
Caribou Biosciences, Inc.
Relapsed/Refractory Multiple Myeloma
This is a Phase 1 study to evaluate the safety of CB-011 (the study treatment), an
allogeneic chimeric antigen receptor (CAR-T) cell therapy that targets the B cell
maturation antigen (BCMA), to determine the best dose of CB-011, and to assess the
effectiveness of CB-011 in treating multiple myelom1 expand
This is a Phase 1 study to evaluate the safety of CB-011 (the study treatment), an allogeneic chimeric antigen receptor (CAR-T) cell therapy that targets the B cell maturation antigen (BCMA), to determine the best dose of CB-011, and to assess the effectiveness of CB-011 in treating multiple myeloma that has come back (relapsed) or that is no longer responding to other treatment (refractory). Type: Interventional Start Date: Feb 2023 |
CRISPR-Edited Allogeneic Anti-CD19 CAR-T Cell Therapy for Relapsed/Refractory B Cell Non-Hodgkin Ly1
Caribou Biosciences, Inc.
Lymphoma, Non-Hodgkin
Relapsed Non Hodgkin Lymphoma
Refractory B-Cell Non-Hodgkin Lymphoma
Non Hodgkin Lymphoma
Lymphoma
CB010A is a study evaluating safety, emerging efficacy, pharmacokinetics and
immunogenicity of CB-010 in adults with relapsed/refractory B cell non-Hodgkin lymphoma
after lymphodepletion consisting of cyclophosphamide and fludarabine. expand
CB010A is a study evaluating safety, emerging efficacy, pharmacokinetics and immunogenicity of CB-010 in adults with relapsed/refractory B cell non-Hodgkin lymphoma after lymphodepletion consisting of cyclophosphamide and fludarabine. Type: Interventional Start Date: May 2021 |
CERAMENTâ„¢| Bone Void Filler Device Registry
BONESUPPORT AB
Orthopedic Disorder
A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in
normal use. expand
A device registry to compile data on the performance of CERAMENT BONE VOID FILLER in normal use. Type: Observational [Patient Registry] Start Date: Mar 2020 |
A Phase 3 Study Evaluating Efficacy and Safety of Lanifibranor Followed by an Active Treatment Exte1
Inventiva Pharma
NASH - Nonalcoholic Steatohepatitis
This Phase 3 study is conducted to evaluate lanifibranor in adults with NASH and liver
fibrosis histological stage F2 or F3 expand
This Phase 3 study is conducted to evaluate lanifibranor in adults with NASH and liver fibrosis histological stage F2 or F3 Type: Interventional Start Date: Aug 2021 |
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