Source: ClinicalTrials.gov — U.S. National Library of Medicine — A database of privately and publicly funded clinical studies conducted around the world (U.S. National Library of Medicine, public domain).
This page lists clinical trials related to Vascular Diseases from the ClinicalTrials.gov database.
Trial Summary
- Total studies: 50
- Recruiting: 27
- Active, not recruiting: 10
- Completed: 7
- Other: 6
Results are refreshed periodically and may not reflect the most current information available from ClinicalTrials.gov.
Recruiting Trials
NCT00006518 — Specimen Collections From Participants With HIV Infection, KSHV Infection, Viral-Related Pre-malignant Lesions and Cancer
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1029 |
| Study Type | OBSERVATIONAL |
| Conditions | HIV; Kaposi’s Sarcoma; Lymphomas; Multicentric Castleman’s Disease; Primary Effusion Lymphoma |
BACKGROUND:
- A number of important scientific advances can be made through the study of blood, bone marrow, tumor, or other tissue samples from patients with HIV infection, infection with Kaposi s sarcoma associated herpesvirus (KSHV), infection with other oncogenic viruses, or cancer.
- This protocol provides a mechanism to affect a variety of such studies.
OBJECTIVES:
-Acquisition of seru…
NCT00923507 — Natural History Study of Monoclonal B Cell Lymphocytosis (MBL), Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL), Lymphoplasmacytic Lymphoma (LPL)/Waldenstrom Macroglobulinemia (WM), and Splenic Marginal Zone Lymphoma (SMZL)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Waldenstrom Macroglobulinemia; Lymphoplasmacytic Lymphoma; Monoclonal B-Cell Lymphocytosis; Small Lymphocytic Lymphoma; CLL (Chronic Lymphocytic Leukemia) |
Background
The development of new technologies now allow scientists to investigate the molecular basis and clinical manifestations of monoclonal B cell lymphocytosis (MBL), chronic lymphocytic leukemia(CLL)/small lymphocytic lymphoma (SLL), lymphoplasmacytic lymphoma (LPL)/Waldenstrom macroglobulinemia (WM), and splenic marginal zone lymphoma (SMZL). Applying these methods in a natural history…
NCT01621594 — Evaluating New Radiation Techniques for Cardiovascular Imaging
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 5000 |
| Study Type | INTERVENTIONAL |
| Conditions | Coronary Disease |
| Interventions |
Title: Evaluating New Radiation Techniques for Cardiovascular Imaging
Background:
Cardiac CT angiography is associated with radiation exposure. Different methods of creating CT pictures have been developed to reduce the radiation dose to the subject. The purpose of this research study is to learn whether these low dose research imagings are accurate or predict subject outcomes.
Cardiac CT is…
NCT02089789 — Clinical and Basic Investigations Into Known and Suspected Congenital Disorders of Glycosylation
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Human Genome Research Institute (NHGRI) |
| Enrollment | 200 |
| Study Type | OBSERVATIONAL |
| Conditions | Congenital Disorders of Glycosylation |
Background:
- Proteins, fats, and other molecules are the body s building blocks. Many of these molecules must have sugars, or chains of sugars, attached to work properly. People with congenital disorders of glycosylation (CDGs) cannot attach these sugars or sugar chains properly. A child or adult with a CDG can have symptoms in different parts of the body, including brain, nerves, muscles, l…
NCT02257866 — Studies of the Natural History, Pathogenesis, and Outcome of Idiopathic Systemic Vasculitis
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS) |
| Enrollment | 4000 |
| Study Type | OBSERVATIONAL |
| Conditions | Takayasu’s Arteritis; Giant Cell Arteritis; Polyarteritis Nodosa; Relapsing Polychondritis; ANCA-Associated Vasculitis |
Background:
- Vasculitis is a group of diseases that inflame and damage blood vessels and tissue. It can cause many medical problems. Few tests can diagnose the disease, and none can reliably predict a relapse. Researchers want to study people s genes and follow people over time to see how the disease affects them.
Objective:
- To learn the signs, symptoms, imaging tests, genetic markers, …
NCT03869138 — Alternative Therapies for Improving Physical Function in Individuals With Stroke
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Illinois at Chicago |
| Enrollment | 120 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke |
| Interventions |
Neurological impairment is a devastating disease for patients and their families and a leading cause of adult disability. Traditional rehabilitative therapies can help regain motor function and ameliorate disability. However, health care reimbursed rehabilitation is usually provided for up to 6 months post stroke (3 months in form of inpatient therapy and 3 months in outpatient therapy). There …
NCT04902443 — Pomalidomide and Nivolumab in People With Virus-Associated Malignancies With or Without HIV
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 58 |
| Study Type | INTERVENTIONAL |
| Conditions | Viral Associated Malignancies; Kaposi Sarcoma; EBV/KSHV-associated Lymphomas |
| Interventions | ; |
Background:
Less toxic and more effective treatments are needed for cancers caused by viruses. These cancers include Hodgkin and non-Hodgkin lymphoma, hepatocellular carcinoma, head and neck cancer, nasopharyngeal carcinoma, gastric cancer, anal cancer, cervical cancer, vaginal cancer, vulvar cancer, penile cancer, Merkel cell carcinoma, Kaposi sarcoma, and leiomyosarcoma. Researchers want to …
NCT05137054 — A Study to Examine the Effects of Novel Therapy Linvoseltamab in Combination With Other Cancer Treatments for Adult Participants With Multiple Myeloma That is Resistant to Current Standard of Care Treatments
| Status | Recruiting |
| Phase | Phase 1 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 317 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma |
| Interventions | ; ; |
This study is researching an experimental drug called linvoseltamab in combination with other drugs for the treatment of a blood cancer called multiple myeloma. Linvoseltamab has previously been studied as a single agent (without other cancer treatments) in participants with multiple myeloma that returned after prior therapies and needed to be treated again.
In the initial study, some particip…
NCT06352632 — ACT-GLOBAL Adaptive Platform Trial for Stroke
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | The George Institute |
| Enrollment | 20000 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke |
| Interventions | ; ; |
Stroke is causing 6.6 million deaths and is a major cause of disability worldwide in 2019. There remains an urgent need for interventions that improve outcomes which can be implemented with wide applicability for stroke. ACT-GLOBAL is a multi-factorial, multi-arm, multi-stage, randomised, global adaptive platform trial for stroke, aiming to identify the treatment/s associated with the highest c…
NCT06352619 — Third Enhanced Control of Hypertension and Thrombectomy Stroke Domain Within ACT-GLOBAL Adaptive Platform Trial
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The George Institute |
| Enrollment | 2000 |
| Study Type | INTERVENTIONAL |
| Conditions | Ischemic Stroke, Acute |
| Interventions | ; ; |
Several clinical trials have produced variable conclusions regarding the effects of intensive blood pressure (BP) lowering in post-EVT acute ischaemic stroke (AIS) patients. Although two trials indicate harm from very intensive target-based treatment (SBP <130 mmHg), the others neutral effects in the SBP range 140-160 mmHg. The ENCHANTED3/MT domain of the ACT-GLOBAL platform trial aims to test…
NCT06588634 — The PERSEVERE Study
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Inari Medical |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Pulmonary Embolism; Pulmonary Thromboembolism |
| Interventions | ; |
Randomized Controlled Trial of High-Risk Pulmonary Embolism Comparing FlowTriever System vs. Standard of Care
NCT06909565 — Inclisiran Versus Placebo for the Prevention of Major Adverse Cardiovascular and Limb Events in Patients Undergoing Percutaneous Coronary Intervention or Peripheral Endovascular Intervention
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Duke University |
| Enrollment | 6000 |
| Study Type | INTERVENTIONAL |
| Conditions | Percutaneous Coronary Intervention; Peripheral Endovascular Intervention |
| Interventions | ; |
V-INTERVENTION will evaluate the effectiveness of inclisiran in preventing major cardiovascular and limb events in patients receiving percutaneous coronary or peripheral arterial revascularization. Inclisiran is a subcutaneous, twice-yearly injection that is FDA-approved as an adjunct with statin therapy and on the market to lower LDL-C in high-risk populations.
NCT01311323 — Revascularization Strategies in Patients With Non-ST-Segment Elevation Acute Coronary Syndrome (NSTE-ACS) and Severe Coronary Artery Disease
| Status | Recruiting |
| Phase | N/A |
| Sponsor | American Heart of Poland |
| Enrollment | 1000 |
| Study Type | INTERVENTIONAL |
| Conditions | Multivessel Coronary Artery Disease; Acute Coronary Syndrome |
| Interventions | ; |
MILESTONE STUDY is dedicated to problems connected with patients with multivessel coronary artery disease and/or with left main narrowing who present symptoms of acute ischemia. For such kind of patients according to current ACC/AHA guidelines CABG (surgical revascularization) is recommended as a treatment method. In comparison with CABG, recent studies have shown that PCI (percutaneous coronar…
NCT06736899 — Trial of Orbital Atherectomy Versus Standard Strategy in Calcified Bifurcation Lesions
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Fundación EPIC |
| Enrollment | 200 |
| Study Type | INTERVENTIONAL |
| Conditions | Coronary Artery Disease; Coronary Disease |
| Interventions | ; |
Clinical research with medical devices indicated in accordance with the CE marking, led by researchers, multicenter, open, prospective, randomized and controlled. Patients are randomized to treatment with a conventional balloon and then a coronary stent or to initial plaque modification with Orbital Atherectomy (OA) and then a coronary stent. To evaluate the efficacy and safety of OA in the ade…
NCT05979168 — Effectiveness and Adoption of the TelTex4BP Intervention Among Adults With Hypertension in Nepal
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Central Department of Public Health |
| Enrollment | 500 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension; Medication Adherence; Blood Pressure; Cardiovascular Diseases |
| Interventions |
Despite evidence of preventing cardiovascular disease (CVD) risk through lifestyle changes, many patients with hypertension (HTN) do not comply with this and suffer from CVD and other complications. A previous study using a structured lifestyle intervention program has reported a 14% decrease in the 10-year risk of developing CVD at one year among hypertensive and diabetes patients. Low and Mid…
NCT07220538 — A Study Testing How Well the Drug Extract of Ginkgo Biloba Leaves Tablets Works for People With Memory or Thinking Problems After a Stroke When Added to Standard Treatment
| Status | Recruiting |
| Phase | Phase 4 |
| Sponsor | Dr. Willmar Schwabe GmbH & Co. KG |
| Enrollment | 400 |
| Study Type | INTERVENTIONAL |
| Conditions | Ischemic Stroke Hospitalized; Impairment, Cognitive |
| Interventions | ; |
The goal of this clinical trial is to learn if Extract of Ginkgo Biloba Leaves Tablets help improve thinking and memory in people aged 55 years and older who had an ischemic stroke (a type of stroke caused by a blocked blood vessel in the brain). It will also look at how safe the Extract of Ginkgo Biloba Leaves Tablets are.
The main questions it aims to answer are:
- Do the Extract of Ginkgo …
NCT07691411 — An Ecological Momentary Assessment Based Program to Support Self-Management for Post-stroke Patients
| Status | Recruiting |
| Phase | N/A |
| Sponsor | The Hong Kong Polytechnic University |
| Enrollment | 50 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke; Post Stroke |
| Interventions |
The goal of this feasibility study is to test whether a new approach that combines real-time symptom tracking (Ecological Momentary Assessment) with machine learning can help people recovering from a stroke to better manage depression, thinking difficulties, and daily functioning. The main questions it aims to answer are:
Is this combined approach practical and acceptable for post-stroke survi…
NCT07517263 — An Open Label Extension (OLE) Study (Following Completion of CTQJ230A12301) to Evaluate Long-term Safety and Tolerability of Pelacarsen (TQJ230)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Novartis Pharmaceuticals |
| Enrollment | 5700 |
| Study Type | INTERVENTIONAL |
| Conditions | Cardiovascular Disease and Lipoprotein(a) |
| Interventions |
This open-label extension study will provide post-trial access to pelacarsen (TQJ230) to participants who have successfully completed the double-blind parent study (CTQJ230A12301).
NCT07296744 — Pivotal Study of the SUpira System in Patients Undergoing High-Risk Percutaneous COronaRy InTervention (HRPCI)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Supira Medical |
| Enrollment | 358 |
| Study Type | INTERVENTIONAL |
| Conditions | Coronary Artery Disease; High Risk Percutaneous Coronary Intervention; Interventional Cardiology; Mechanical Circulatory Support |
| Interventions | ; |
The objective of this study is to assess the safety and efficacy of the Supira System in providing temporary cardiovascular hemodynamic support in patients undergoing HRPCI. Eligible patients will be randomized to undergo HRPCI with either the Supira System (investigational device) or the commercially available Impella systems (comparator device).
NCT07393282 — A Study to Compare Linvoseltamab and Daratumumab Treatment in High-Risk Smoldering Multiple Myeloma (HR-SMM)
| Status | Recruiting |
| Phase | Phase 3 |
| Sponsor | Regeneron Pharmaceuticals |
| Enrollment | 270 |
| Study Type | INTERVENTIONAL |
| Conditions | High Risk Smoldering Multiple Myeloma (HR-SMM) |
| Interventions | ; |
This study is researching an experimental drug called linvoseltamab (also called “study drug”) compared to another drug called daratumumab, in participants with Smoldering Multiple Myeloma (SMM), who are at a High Risk (HR) of developing active multiple myeloma.
The aim of this study is to find out whether linvoseltamab is better than daratumumab in delaying the development of MM.
The study i…
NCT07592273 — Surabgene Lomparvovec Administered in the Suprachoroidal Space in Adult Participants With Diabetic Retinopathy Without Center-Involved Diabetic Macular Edema
| Status | Recruiting |
| Phase | Phase 2 / Phase 3 |
| Sponsor | AbbVie |
| Enrollment | 576 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetic Retinopathy |
| Interventions | ; ; |
Diabetic Retinopathy (DR) is a common eye condition caused by diabetes, where high blood sugar levels damage the blood vessels in the back part of the eye (called the retina). Over time, this damage can lead to vision problems and even blindness if not treated. This study will assess surabgene lomparvovec (sura-vec) as a potential one-time gene therapy administered in the suprachoroidal space (…
NCT07689058 — CAR-T in Relapsed/Refractory Multiple Myeloma
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Dr. Zaineb Akram |
| Enrollment | 10 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma Refractory; Multiple Myeloma in Relapse |
| Interventions |
The treatment options for multiple myeloma have evolved significantly over the years, providing patients with a range of therapies tailored to their specific circumstances. The choice of treatment often hinges on various factors, including the aggressiveness of the disease, individual prognostic indicators like genetic markers, the overall physical condition of the patient, and any pre-existing…
NCT07054801 — IA Lidocaine and Methylprednisolone for Headache Associated With Subarachnoid Hemorrhage
| Status | Recruiting |
| Phase | Phase 2 |
| Sponsor | Daniel Raper, MBBS |
| Enrollment | 25 |
| Study Type | INTERVENTIONAL |
| Conditions | Headaches Associated With Subarachnoid Hemorrhage (SAH) |
| Interventions | ; |
Subarachnoid hemorrhage (SAH) is a type of bleeding around the brain that can cause sudden and severe headaches. These headaches can be debilitating and persist for weeks, significantly impacting a patient’s comfort and recovery. Many patients require opioids for pain control, which can lead to side effects such as drowsiness, constipation, and dependency. There is a need for new treatment stra…
NCT07631078 — kTMP-Enhanced Motor Rehabilitation for Chronic Stroke Recovery (KULMINATE) Pilot
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Magnetic Tides |
| Enrollment | 12 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke; Chronic Stroke Patients; Arm Weakness as a Consequence of Stroke |
| Interventions | ; |
kTMP, kilohertz transcutaneous magnetic perturbations, is a low intensity transcranial magnetic stimulation technique that will be used in this study to promote arm/hand rehabilitation in patients who have been disabled by stroke.
NCT07649135 — Feasibility of a Remotely Delivered Step Count Intervention in Chronic Stroke
| Status | Recruiting |
| Phase | N/A |
| Sponsor | University of Minnesota |
| Enrollment | 24 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke; Ischemic Stroke; Hemorrhagic Stroke |
| Interventions |
The goal of this study is to explore the feasibility of a new approach to rehabilitation that focuses on step count. Participants will complete 6 telephone or Zoom-based sessions with an occupational therapist over 6 weeks and use a step count tracker during that time. They will also complete questionnaires, assessments, surveys, and physical activity measurements during study weeks 0 (baseline…
NCT06615973 — Screening for Social Determinants of Health (SDOH) and Cognitive Function in Individuals With History of Stroke
| Status | Recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 450 |
| Study Type | OBSERVATIONAL |
| Conditions | Stroke; Brain Disease; Vascular Diseases; Cerebrovascular Disorder |
Background:
Stroke is the fifth leading cause of death in the United States. It is also a leading cause of disability. More than 70% of people who survive strokes have mental impairment or dementia. Medical factors, such as the severity of the stroke, affect whether a person will have mental impairment afterward. But social factors, such as education and ethnicity, seem to play a role as well….
NCT07521930 — Interfacing With NeuroTechnology to Expand Neural Throughput (INTENT)
| Status | Recruiting |
| Phase | N/A |
| Sponsor | Johns Hopkins University |
| Enrollment | 5 |
| Study Type | INTERVENTIONAL |
| Conditions | Tetraplegia/Tetraparesis; Amyotrophic Lateral Sclerosis (ALS); Muscular Disorders, Atrophic; Brain Stem Stroke; Spinal Cord Injuries (SCI) |
| Interventions |
The goal of this clinical trial is to evaluate the safety and preliminary efficacy of an implantable device that records and stimulates different areas of the brain to allow adults affected by disabling paralysis (see Eligibility for more details) to control and receive feedback from assistive devices.
Active, Not Recruiting
NCT00005398 — University of North Carolina Alumni Heart Study
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | Duke University |
| Enrollment | 6340 |
| Study Type | OBSERVATIONAL |
| Conditions | Cardiovascular Diseases; Heart Diseases; Coronary Disease; Depression |
| Interventions |
To continue surveillance of the participants in the University of North Carolina Alumni Heart Study, which tests the hypothesis that hostility and related psychosocial factors are involved in the pathogenesis of coronary heart disease.
NCT00005902 — Study of Brain and Spinal Cord Tumor Growth and Cyst Development in Patients With Von Hippel Lindau Disease
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 250 |
| Study Type | OBSERVATIONAL |
| Conditions | Hemangioblastoma; Hippel Lindau Disease |
The purpose of this study is to learn more about the growth of brain and spinal cord tumors and cysts that develop in association with them in patients with von Hippel-Lindau disease. It will examine how fast the tumors grow and try to determine what factors (for example, puberty , pregnancy, menopause, blood proteins, etc.) affect their growth.
Patients between the ages of 8 and 75 years who …
NCT01323322 — Healthy Aging in Neighborhoods of Diversity Across the Life Span (HANDLS)
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | National Institute on Aging (NIA) |
| Enrollment | 3720 |
| Study Type | OBSERVATIONAL |
| Conditions | Diabetes; Cerebrovascular Disease; Age-Associated Decline; Cardiovascular Disease |
The Healthy Aging in Neighborhoods of Diversity across the Life Span (HANDLS) study is an interdisciplinary, community-based, prospective longitudinal epidemiologic study examining the influences of race and socioeconomic status (SES) on the development of age-related health disparities among socioeconomically diverse African Americans and whites in Baltimore. This study investigates whether he…
NCT02465060 — Targeted Therapy Directed by Genetic Testing in Treating Patients With Advanced Refractory Solid Tumors, Lymphomas, or Multiple Myeloma (The MATCH Screening Trial)
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 6452 |
| Study Type | INTERVENTIONAL |
| Conditions | Advanced Lymphoma; Advanced Malignant Solid Neoplasm; Bladder Carcinoma; Breast Carcinoma; Cervical Carcinoma |
| Interventions | ; ; |
This phase II MATCH screening and multi-sub-trial studies how well treatment that is directed by genetic testing works in patients with solid tumors, lymphomas, or multiple myelomas that may have spread from where it first started to nearby tissue, lymph nodes, or distant parts of the body (advanced) and does not respond to treatment (refractory). Patients must have progressed following at leas…
NCT03205527 — Perturbation Training for Fall-risk Reduction Among Stroke Survivors
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Illinois at Chicago |
| Enrollment | 91 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke |
| Interventions |
The long-term objective of this research is to develop an efficacious training paradigm to enhance stroke survivors’ defense mechanisms against falls and possibly reduce healthcare cost. The Centers for Disease Control and Prevention estimates the direct medical cost for fall related injuries to be $34 billion annually. Forty percent to 70% of community-dwelling stroke survivors experience detr…
NCT05263934 — Efficacy and Safety of Depemokimab Compared With Mepolizumab in Adults With Relapsing or Refractory Eosinophilic Granulomatosis With Polyangiitis (EGPA)
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | GlaxoSmithKline |
| Enrollment | 163 |
| Study Type | INTERVENTIONAL |
| Conditions | Eosinophilic Granulomatosis With Polyangiitis |
| Interventions | ; ; |
This study aims to investigate the efficacy and safety of depemokimab compared with mepolizumab in adults with relapsing or refractory EGPA receiving SoC therapy.
NCT06094491 — Virtual Diabetes Group Visits Across Health Systems
| Status | Active, not recruiting |
| Phase | N/A |
| Sponsor | University of Chicago |
| Enrollment | 720 |
| Study Type | INTERVENTIONAL |
| Conditions | T2DM (Type 2 Diabetes Mellitus); Hypertension; Heart Disease Chronic; Stroke; Hyperlipidemias |
| Interventions |
The purpose of this project is to evaluate the effectiveness of a virtual diabetes group visits on patients with type 2 diabetes mellitus (T2DM).
NCT06321302 — A Study to Test Whether BI 764524 Helps People With an Eye Condition Called Diabetic Retinopathy
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | Boehringer Ingelheim |
| Enrollment | 190 |
| Study Type | INTERVENTIONAL |
| Conditions | Diabetic Retinopathy |
| Interventions | ; ; |
This study is open to adults with diabetic retinopathy. People who have non-proliferative diabetic retinopathy of moderate or high severity can join the study.
The purpose of this study is to find out whether a medicine called BI 764524 helps people with diabetic retinopathy. The study also aims to find a suitable treatment plan for BI 764524. Participants are put into 5 groups by chance. Part…
NCT06169215 — Comparing the Combination of Selinexor-Daratumumab-Velcade-Dexamethasone (Dara-SVD) With the Usual Treatment (Dara-RVD) for High-Risk Newly Diagnosed Multiple Myeloma
| Status | Active, not recruiting |
| Phase | Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 70 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma |
| Interventions | ; ; |
This phase II trial compares the combination of selinexor, daratumumab and hyaluronidase-fihj (daratumumab), velcade (bortezomib), and dexamethasone (Dara-SVD) to the usual treatment of daratumumab, lenalidomide, bortezomib, and dexamethasone (Dara-RVD) in treating patients with high-risk newly diagnosed multiple myeloma. Selinexor is in a class of medications called selective inhibitors of nuc…
NCT06413498 — A Study Comparing Anitocabtagene Autoleucel to Standard of Care Therapy in Participants With Relapsed/ Refractory Multiple Myeloma
| Status | Active, not recruiting |
| Phase | Phase 3 |
| Sponsor | Kite, A Gilead Company |
| Enrollment | 452 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma |
| Interventions | ; ; |
The goal of this study (iMMagine-3) is to compare the study drug, anitocabtagene autoleucel to standard of care therapy (SOCT) in participants with relapsed/refractory multiple myeloma who have received 1 to 3 prior lines of therapy, including an anti-CD38 monoclonal antibody and an immunomodulatory drug.
The primary objective of this study is to compare the efficacy of anitocabtagene autoleuc…
Not Yet Recruiting
NCT07690982 — Assessing Posture and ROM With PhysioMaster in Stroke Patients
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Istinye University |
| Enrollment | 60 |
| Study Type | OBSERVATIONAL |
| Conditions | Stroke |
The smartphone application named PhysioMaster is an easy-to-use, accessible, and freely available application. Although it has been used in several previous studies, no validity or reliability study has yet been conducted in patients with stroke. Therefore, the aim of this study is to investigate the validity and reliability of the PhysioMaster smartphone application in patients with stroke.
A…
NCT07689591 — Noninvasive Artificial Venous Stasis for Reperfusion in STEMI
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Firat University |
| Enrollment | 500 |
| Study Type | OBSERVATIONAL |
| Conditions | STEMI - ST Elevation Myocardial Infarction |
This prospective, randomized study was designed to evaluate whether the noninvasive artificial venous stasis / RE-START procedure, administered prior to primary percutaneous coronary intervention, increases the frequency of spontaneous coronary reperfusion in the infarct-related artery.
NCT07690020 — Clinical Efficacy and Mechanism Research of Getong Tongluo Capsule in Ischemic Stroke
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Nanfang Hospital, Southern Medical University |
| Enrollment | 216 |
| Study Type | INTERVENTIONAL |
| Conditions | Ischemic Stroke, Acute |
| Interventions | ; ; |
The purpose of this single-center, randomized, double-blind, controlled trial is to clarify the clinical efficacy and safety of Getong Tongluo Capsule in patients with ischemic stroke. Combined with gut microbiome and metabolomics techniques, investigators will explore whether this medicine exerts neuroprotective effects via the gut-brain axis. Investigators will further verify its pharmacologi…
NCT07691034 — Monitoring MRD in Multiple Myeloma in Serum by Mass Spectrometry
| Status | Not yet recruiting |
| Phase | N/A |
| Sponsor | Odense University Hospital |
| Enrollment | 40 |
| Study Type | OBSERVATIONAL |
| Conditions | Multiple Myeloma; Minimal Residual Disease |
| Interventions |
Multiple myeloma (MM) is a severe plasma cell cancer caused by proliferation and accumulation of malignant plasma cells in the bone marrow. Novel therapies have improved responses and survival considerably. Recently, it was shown that achieved and sustained minimal residual disease (MRD) negativity is the best predictor for long-term disease-free and overall survival. Achieving and maintaining …
Enrolling by Invitation
NCT02473757 — Gene Therapy Follow-up Protocol for People Previously Enrolled in CAR-T Cell Studies
| Status | Enrolling by invitation |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1000 |
| Study Type | OBSERVATIONAL |
| Conditions | Lyphoma, B-Cell; Leukemia, B-cell; Multiple Myeloma; Hematologic Malignancies |
Background:
- Gene therapy is a way to treat or prevent disease using genes. It is monitored very closely by regulators because there can be long-term, unexpected side effects. NIH is required to try to contact people who have been treated with gene therapy at least annually for up to 15 years. This is to see if they have had any bad side effects. This trial does not include any therapy and i…
Completed Trials
NCT01139476 — Specimen Collection for Agricultural Health Study Cohort Pesticide Exposure Study
| Status | Completed |
| Phase | N/A |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 1892 |
| Study Type | OBSERVATIONAL |
| Conditions | Multiple Myeloma; Leukemia; MGUS; Monoclonal B-Cell Lymphocytosis |
Background:
- Multiple myeloma (MM), a type of cancer that affects the white blood cells, is often preceded by a precancerous disorder known as monoclonal gammopathy of undetermined significance (MGUS). Farmers and other agricultural workers have a higher risk of developing MGUS and MM, possibly because of their exposure to certain pesticides. Researchers are interested in studying biological…
NCT01132937 — Evaluation, Pathogenesis, and Outcome of Subjects With or Suspected Traumatic Brain Injury
| Status | Completed |
| Phase | N/A |
| Sponsor | National Institute of Neurological Disorders and Stroke (NINDS) |
| Enrollment | 886 |
| Study Type | OBSERVATIONAL |
| Conditions | Traumatic Brain Injury |
Background:
- Traumatic brain injury may have a range of effects, from severe and permanent disability to more subtle functional and cognitive deficits that often go undetected during initial treatment. To improve treatments and therapies and to provide a uniform quality of care, researchers are interested in developing more standardized criteria for diagnosing and classifying different types…
NCT02311335 — Genes Involved in Lipid Disorders
| Status | Completed |
| Phase | N/A |
| Sponsor | National Heart, Lung, and Blood Institute (NHLBI) |
| Enrollment | 140 |
| Study Type | OBSERVATIONAL |
| Conditions | Lipid Disorders |
Background:
- Genes are the instructions our body uses to function. Researchers can look for changes, or variants, in the genes. The goal of this study is to find new gene changes that lead to lipid disorders. Older research methods looked at one or a few genes at a time. Genomic sequencing looks at most of the genes at once. Genomic sequencing may find the cause researchers haven t been able…
NCT05509569 — A Survey of Icatibant in Pediatric Participants With Hereditary Angioedema
| Status | Completed |
| Phase | N/A |
| Sponsor | Takeda |
| Enrollment | 32 |
| Study Type | OBSERVATIONAL |
| Conditions | Hereditary Angioedema (HAE) |
| Interventions |
This study is a survey in Japan of Icatibant subcutaneous injection 30 mg syringe used to treat children or teenagers with acute attacks of hereditary angioedema (HAE). The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study.
The main aim of the study is to check for side effects relat…
NCT05393232 — Groceries for Black Residents of Boston to Stop Hypertension Among Adults With Treated Hypertension
| Status | Completed |
| Phase | N/A |
| Sponsor | Beth Israel Deaconess Medical Center |
| Enrollment | 176 |
| Study Type | INTERVENTIONAL |
| Conditions | Hypertension |
| Interventions | ; |
GoFreshRx is a randomized trial, testing the effects of a home-delivered DASH-patterned grocery intervention on blood pressure in Black adults actively treated for hypertension, residing in Boston area urban food deserts.
NCT05559398 — Glenzocimab for REperfusion in the Setting of Endovascular Therapy for Brain infarctioN: GREEN Study
| Status | Completed |
| Phase | Phase 2 / Phase 3 |
| Sponsor | Assistance Publique - Hôpitaux de Paris |
| Enrollment | 108 |
| Study Type | INTERVENTIONAL |
| Conditions | Stroke, Acute; Stroke, Ischemic |
| Interventions | ; |
Emergent reperfusion is the main goal for acute ischemic stroke therapy (AIS). Endovascular therapy (EVT) is recommended within 6 hrs of stroke onset, and up to 24 hrs following perfusion imaging criteria.
Despite the major benefit associated with MT, more than 50% of the patients remain disabled at 3 months. Reperfusion rates after MT are critical to determine functional outcome. However, com…
NCT06495996 — The Protrieve PROTECTOR Study
| Status | Completed |
| Phase | N/A |
| Sponsor | Inari Medical |
| Enrollment | 66 |
| Study Type | INTERVENTIONAL |
| Conditions | Venous Thromboembolism; Deep Venous Thrombosis |
| Interventions |
The Protrieve PROTECTOR Study is a prospective, single-arm, multicenter study of the Protrieve Sheath.
Other (Suspended)
NCT06876142 — Combination Therapy (Mirdametinib and Sirolimus) for RAS Mutated Relapsed Refractory Multiple Myeloma
| Status | Suspended |
| Phase | Phase 1 / Phase 2 |
| Sponsor | National Cancer Institute (NCI) |
| Enrollment | 54 |
| Study Type | INTERVENTIONAL |
| Conditions | Multiple Myeloma; Relapsed and/or Refractory Multiple Myeloma (RRMM) |
| Interventions | ; |
Background:
Multiple myeloma (MM) is a type of blood cancer that affects a person s immunity. MM returns after treatment (relapse) in almost all people; MM may also not respond to initial treatment (refractory). Many people with relapsed refractory MM (RRMM) also have changes in their KRAS and NRAS genes. Researchers want to try a new drug treatment that targets cancer with these changed genes…