Clinical trials

85

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Establishing Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1) Extension

Myotonic Dystrophy type 1 (DM1) is an autosomal dominant multisystemic disorder that causes progressive disability and shortened life expectancy. It is characterized by progressive weakness and myotonia, which preferentially affects the craniofacial, hand, and distal leg muscles. Many patients also experience difficulties with cognition, cardiac arrhythmias, respiratory failure, or cataracts. Currently there is no treatment to slow progression or reverse the symptoms.

Participants needed: 1,000
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Jul 13, 2026Locations: 1Duration: 4 Years
Eligibility criteria

Age 18 to 70 years (inclusive) [+2]

Symptomatic renal or liver disease, uncontrolled diabetes or thyroid disorder, o... [+4]

Status: Recruiting

Cardiovascular Health Education Via Virtual Reality for Breast Cancer Survivors Receiving Anthracyclines or Trastuzumab

The main goal of this study is to test a virtual reality (VR) program, Survivors' Virtual Reality Survivorship Experience (SurviVRSE), designed to help Breast Cancer survivors (n=30) learn about heart health. The aims are to test the usability, feasibility, and acceptability o the intervention. Additionally, follow-up assessments will examine changes in women's cancer therapy related cardiac dysfunction knowledge and heart healthy behaviors (e.g., physical activity).

Participants needed: 30
Trial details
Age: 18+Biological sex: FemaleType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jul 2, 2026Locations: 3
Eligibility criteria

18 years of age or older [+4]

Status: Recruiting

A Hospital-based Intervention for Youth Injured Through Violence

The firearm violence epidemic is a major public health problem, especially for youth. Every day in the US, approximately 100 people fall casualty to firearms through forms of violence, such as homicide, suicide, and unintentional or accidental injuries. Among youth, firearm violence remains the leading cause of death, and each year the rate of firearm-related mortality is increasing. Beyond the significant and devastating cost of human life, firearm violence is an enormous economic burden to the US, which totals an estimated $229 billion annually. In urban communities with high rates of firearm-related violence, firearm-related emergency department visits are extremely draining on the hospital system. At the national level, firearm-related injuries account for $2.8 billion annually in emergency department care each.

Participants needed: 360
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

Aged 13-17 years old [+1]

Youth aged <13 years and >17 years old [+2]

Status: Recruiting

Safety and Efficacy of LOw DOse COlchicine in Patients With STatin INTolerance: the LODOCO STINT Pilot Study

Statins are a class of cholesterol lowering medications that contribute to reducing a person's risk of experiencing a cardiovascular event like heart attack. Along with the ability to lower cholesterol, statins also possess anti-inflammatory properties which contribute to their cardioprotective effects. Some people experience side effects while taking statins and are unable to continue treatment with them,which can then increase a person's risk of having cardiovascular issues due to untreated high cholesterol levels. Prior studies have shown that inflammation in the body may lead to an increased risk of a future cardiovascular events. Low dose colchicine (LODOCO), an anti-inflammatory agent, has been shown to reduce cardiovascular events by inhibiting inflammation, a major cause of cardiovascular disease. The United States Food and Drug Administration (FDA) has approved LODOCO to reduce the risk of a future cardiac events for those who have existing heart disease or possess multiple risk factors for heart disease.

Participants needed: 30
Trial details
Phase: Phase 1Age: 18-80Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

History of statin intolerance (As defined by the NLA 2023 guidelines) Patients w... [+3]

Known hypersensitivity to colchicine, current use of colchicine or other anti-in... [+9]

Status: Recruiting

Comprehensive Tobacco Cessation for Cancer Patients and Survivors

The purpose of this research study is to learn how best to incorporate tobacco cessation treatment into clinical care for cancer patients, survivors, and caregivers.

Participants needed: 75
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Provision of signed and dated informed consent form [+3]

Not a VCUHealth patient [+1]

Status: Recruiting

Examining the Impact of Exercise Training on Vascular Dysfunction in Individuals With Mental Health Disorders - Study 1

The purpose of this research study is to examine the role oxidants, substances produced in the blood that can damage blood vessel function, may play in blood vessel function in healthy individuals as well as individuals with mental health disorders (posttraumatic stress disorder (PTSD) and/or generalized anxiety disorder (GAD)).

Participants needed: 720
Trial details
Age: 18-35Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jul 1, 2026Locations: 1
Eligibility criteria

apparently healthy and free of overt cardiovascular, pulmonary, or metabolic dis... [+3]

taking medications that could influence cardiovascular function [+5]

Status: Recruiting

Total Neoadjuvant Therapy With mFOLFOX and Short-course Radiation in Resectable Rectal Cancer

This is phase 2 trial of neoadjuvant therapy and short-course radiotherapy in resectable rectal cancer.

Participants needed: 64
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jul 1, 2026Locations: 4
Eligibility criteria

Pathologic diagnosis of adenocarcinoma of the rectum (diagnosis by tissue biopsy... [+16]

Prior RT that would result in unsafe overlap of RT fields with the planned study... [+10]

Status: Not yet recruiting

TENS of Auricular Vagal Nerve for Radiation Necrosis

This is a multi-center, randomized, blinded trial evaluating the effect of transcutaneous auricular vagal nerve stimulator (taVNS) on radiation necrosis-related cerebral edema. In this study, consenting and eligible patients will be assigned to one of two arms: treatment (Arm 1) or sham (Arm 2). Patients in both arms will have imaging performed and tissue and blood collected for assessment of changes in area of contrast enhancement and cerebral edema, inflammatory markers, and markers of blood-brain barrier permeability.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jul 2, 2026Locations: 1
Eligibility criteria

History of glioma or metastatic brain lesion previously treated with whole brain... [+4]

New onset neurologic deficits secondary to radiation necrosis requiring initiati... [+5]

Status: Recruiting

Alveolar Ridge Preservation (ARP) in the Posterior Maxilla After the Extraction of Maxillary Molars

Dental implants are a fixed replacement solution with reported long-term survival rates between 94-98% over 20-40 years. In order to ensure successful implant therapy, adequate bone and soft tissue as well as correct 3D positioning of the implant are required. Upon extraction of a tooth, socket width can decrease by up to 60% within six months post-extraction, with a 11-22% vertical reduction. Additionally, sinus pneumatization occurs post-extraction as the maxillary sinus expands into the empty socket due to disuse atrophy and intra-sinus air pressure, as explained by Wolff's law. This further reduces residual bone height (RBH), often resulting in posterior maxillary sites requiring supplemental procedures to prevent bone loss or to augment the bone height at the time of implant placement. However, if the bone height and width dimensions are sufficient before and after extraction - in that, even with the aforementioned loss in width and height percentages in the latter, a standard implant may still be placed in the surrounding bone, one can argue that grafting may not be necessarily done at the time of extraction. Rather, it can be tailored to the patients' needs; thus potentially reducing overall post-operative discomfort and pain.

Participants needed: 40
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 26, 2026Locations: 1
Eligibility criteria

Intact or <5mm dehiscence buccally and palatally [+1]

Medically compromised [+2]

Status: Recruiting

Immune Registry for BK in Kidney Transplant Recipients

Kidney transplantation (KT) is the best treatment modality available to date for patients with advanced kidney disease and the success of KT is dependent on maintaining a selective intricate balance between the risk of rejection and infections in KT recipients. BK virus is an important clinical infection affecting the post-transplant outcomes in KT recipients. BK nephropathy can affect 8-15% of patients after KT causing acute kidney injury, increased risk of rejection and fibrosis leading to additional hospital stays, increasing overall health care cost burden, and in some cases graft loss. The exact pathogenesis and treatment options for BK nephropathy are not clearly understood. It is debatable whether BK nephropathy is a full fledge donor-derived infection or reactivation of the recipient's latent infection. Irrespective of etiology, the common consensus is that treatment of BK virus infection depends on the selective restoration of host immune responses and balancing the risk of rejection vs worsening of infection.

Participants needed: 60
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Jun 26, 2026Locations: 1Duration: 24 Months
Eligibility criteria

Adult (>18 years old) male and female, deceased donor KT recipients [+3]

Prisoners will not be included in the study [+1]

Status: Not yet recruiting

Safety and Tolerability Study of VVZ-2471 in Healthy Volunteers

The goal of this study is to do follow-up safety testing and how well people are able tolerate an experimental (not FDA approved) medication . This study is seeking non-illicit drug using adults to test the medication. Results of this study will help us to develop future studies to test the medication with people who use substances.

Participants needed: 60
Trial details
Phase: Phase 1Age: 18-65Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 25, 2026Locations: 1
Eligibility criteria

Demographics: Male or female, between 18 and 65 years of age. [+15]

Psychosis and bipolar disorder: Any lifetime history of psychosis or bipolar dis... [+9]

Status: Not yet recruiting

Single FrAction Interstitial BreaSt BracHytherApy

This phase 2, single arm prospective study has been designed to determine the safety of delivering accelerated partial breast irradiation (APBI) with a multicatheter interstitial implant in a single fraction over 1 day. This is a method of delivering radiation therapy directly into or close to a tumor.

Participants needed: 134
Trial details
Phase: Phase 2Age: 40-85Biological sex: FemaleType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 18, 2026Locations: 1
Eligibility criteria

Female [+19]

Pregnant or breastfeeding [+10]

Status: Not yet recruiting

Using Apollo Neuro in Autistic Children With Self-Injurious Behavior

This study will evaluate the feasibility and acceptability of the Apollo Neuro, a wearable vibrotactile sensory device, in autistic children who engage in self-injurious behavior (SIB). Participants will wear the device for at least 3 hours per day over a 30-35 day period with caregiver support. Outcomes will include adherence to device use, caregiver-reported feasibility and acceptability, and descriptive characterization of caregiver-reported self- injurious and repetitive behaviors during the study period. This preliminary, single-group study is not designed to evaluate efficacy and will inform the design of future controlled trials.

Participants needed: 18
Trial details
Age: 6-179Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Diagnosis of autism spectrum disorder (ASD), as reported by caregiver [+4]

implanted medical or neurological devices (e.g., pacemaker) [+9]

Status: Recruiting

The Impact of Chronic E-Cigarette Usage on Microvascular Health

The study is focused on investigating the mechanisms involved in microvascular health in subjects that use e-cigarettes frequently. To explore microvascular health, different techniques and compounds. For one of the tests, iontophoresis, the drug's use will be stored and handled as described by the approved IND and non-IDS plan.

Participants needed: 44
Trial details
Age: 18-29Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

Between 18 and 29 years of age [+1]

17 years old and younger or 30 years old or older. [+11]

Status: Recruiting

Functional Outcomes in CondUction System Pacing and Right Ventricular Synchrony (FOCUS-Right)

The goal of this prospective single center clinical trial is to evaluate the safety and feasibility of performing simultaneous exercise stress cardiac magnetic resonance (CPET-CMR) and cardiopulmonary exercise testing in patients with pre-existing left bundle branch area pacemakers (LBBAP) programmed to an atrial sensing mode. Measurements of right ventricular, left ventricular function, and exercise capacity will be obtained at various LBBAP programming parameters at rest and during low intensity exercise. The main aims of the study are: * Demonstrate the safety and feasibility of performing CPET-CMR in patients with pre-existing LBBAP programmed to P-synchronous ventricular pacing mode. * Generate preliminary data evaluating differences in RV function, LV function, and exercise capacity during various pacemaker programming settings.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 17, 2026Locations: 1
Eligibility criteria

presence of dual chamber LBBAP implantation [+1]

Known history of chronotropic incompetence [+5]

Status: Recruiting

Evaluating Urinary CXCL10 for Enhanced Detection of Acute Rejection in Kidney Transplant Patients With Low DD-CFDNA

Kidney transplant rejection remains a significant challenge to long-term graft survival. While histological biopsy continues to be the gold standard for diagnosing rejection, noninvasive biomarkers such as donor-derived cell-free DNA (dd-cfDNA) have gained traction for their ability to detect allograft injury. However, dd-cfDNA may lack sensitivity in certain clinical scenarios particularly in cases of localized immune activation leading to false negatives despite biopsy-confirmed rejection.

Participants needed: 50
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Age ≥18 years [+7]

Individuals under 18 years of age [+4]

Status: Not yet recruiting

Enhancing an Existing Prevention Strategy to Reduce Intentional Firearm Injuries Among High-risk Youth (Phase 1)

Over the past three decades, substantial resources have been devoted to developing youth violence prevention (YVP) programs. These programs have demonstrated positive effects on reducing aggression and related behaviors, firearm-specific risk factors were largely overlooked due to historical barriers to firearm research. This omission is concerning, as firearms are now the leading cause of injury and death among U.S. youth. Existing YVP strategies such as Emerging Leaders address general violence risk but do not directly target firearm-related risks or suicide prevention. There remains a critical gap in prevention strategies that integrate firearm-specific content while leveraging established program infrastructure.

Participants needed: 45
Trial details
Age: 13-17Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Youth aged approximately 13-17 years. [+3]

Significant cognitive impairment or developmental disability that would preclude... [+1]

Status: Not yet recruiting

Enhancing Addiction Treatment Through Psychoeducation

Addiction is a brain disorder characterized by a broad range of both apparent and subtle cognitive impairments in attention, memory, executive functions, and decision-making. These cognitive problems are clinically significant and may contribute to poor treatment outcomes in people with Substance Use Disorders (SUDs), such as a high risk of dropout, low treatment compliance, and shorter periods of abstinence. Studies on cognitive function in SUDs reveal that chronic use of drugs and alcohol can also negatively affect another crucial component of cognition: awareness, or metacognition. Metacognition is defined as an individual's ability to perceive and understand their cognitive functions and use this understanding to regulate them. One of the key consequences of metacognitive impairments is the lack of insight in people with SUDs, which adversely affects treatment outcomes. Substance users with poor metacognition are more reluctant to initiate or continue treatment and are more likely to deny their cognitive problems. Therefore, improving metacognition may remove or reduce motivational barriers to invest time and effort in the recovery process in general, and in the brain recovery process specifically. Despite the importance of neurocognition and metacognition in the recovery process for substance users, there is a dearth of interventions designed to target these functions.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

current DSM-5 opioid and/or stimulant use disorder [+2]

current psychosis, mania, or suicidal/homicidal ideation [+1]

Status: Recruiting

Advancing Water Security: A Community Participatory School-Based Hydration Intervention

The goal of this study is to determine the effectiveness and sustainability of a community-participatory hydration intervention over 3 years within a district that has newly installed hydration stations and is operating under a policy designed to enhance heathy hydration practices and promote equitable access to drinking water.

Participants needed: 7,200
Trial details
Age: 4+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Lunchroom observations: All students (K-5th [Pre-Kindergarten if applicable]) wh... [+3]

Lunchroom observations: None. [+3]

Status: Recruiting

A Virtual Reality Brief Violence Intervention: Preventing Gun Violence Among Violently Injured Adults

The overall aim of the proposed project is to develop and evaluate the effectiveness of Brief Violence Intervention-Virtual Reality (BVI-VR) for reducing firearm-related violence, re-injury, and mortality among victims of violence. Outcome measures of firearm-related violence will come from multiple sources, including criminal background checks, hospital data, state-level data, semi-structured clinical assessments, and self-report assessments. In addition, the study aims to understand the impact of BVI-VR on psychosocial mediators resulting in a reduction of firearm-related violence. This will include self-report surveys, neurocognitive assessments, and clinical assessments. The economic efficiency of BVI-VR as a firearm-related violence intervention will also evaluated. To achieve these aims, a randomized control trial (RCT) in a large sample of violently injured adults (18+ years) from VCU Health will be conducted.

Participants needed: 220
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

violently injured patients from VCU's Level 1 Trauma Center [+2]

Under 18 years old [+1]

Status: Not yet recruiting

Southeastern ATTR Amyloidosis Consortium: SEATTRAC Family Registry

The study design is a prospective registry including asymptomatic and symptomatic patients who carry a pathogenic TTR mutation. The study will enroll patients who meet the inclusion criteria and none of the exclusion criteria until 1000 patients are enrolled, at which point in time the study investigators will evaluate whether further patient accrual is meaningful.

Participants needed: 1,000
Trial details
Age: 18+Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Jun 9, 2026Locations: 1Duration: 3 Years
Eligibility criteria

Over the age of 18 years [+2]

Patient having undergone heart transplantation or implantation of mechanical cir... [+3]

Status: Not yet recruiting

The Impact of Improved Vagal Function on Periaqueductal Gray Connectivity

This study is being to see if participating in breathing exercise training and practicing this training will help with Postural tachycardia syndrome (POTS). The information may help doctors to learn more about how the different parts of people's brains communicate.

Participants needed: 12
Trial details
Age: 18-50Biological sex: AllType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 9, 2026Locations: 1
Eligibility criteria

Age 18-50 years [+3]

Inflammatory arthritis, connective tissue or auto-immune disorder [+13]

Status: Recruiting

DMCRN-02-001: Assessing Pediatric Endpoints in DM1

The overall goal of the study is to establish valid clinical endpoint assessments for children with congenital myotonic dystrophy type 1 and develop biomarkers for the condition.

Participants needed: 50
Trial details
Age: Up to 59Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Jun 10, 2026Locations: 5
Eligibility criteria

Age neonate to 3 years 11 months at enrollment. [+2]

Any other non-DM1 illness that would interfere with the ability or results of th... [+4]

Status: Recruiting

Estab Biomarkers and Clinical Endpoints in Myotonic Dystrophy Type 1 (END-DM1)

Building on previous work of the Myotonic Dystrophy Clinical Research Network (DMCRN), the present study seeks to overcome insufficient data on natural history; lack of reliable biomarkers; and incomplete characterization and limited biological understanding of the phenotypic heterogeneity of Myotonic Dystrophy 1 by examining strategies to improve the reliability by making further refinements in our sample collection and analysis procedures by developing strategies for managing patient heterogeneity going forward. Funding Source- FDA OOPD

Participants needed: 700
Trial details
Age: 18-70Biological sex: AllType: ObservationalSponsor: Virginia Commonwealth UniversityUpdated: Jun 10, 2026Locations: 17
Eligibility criteria

Age 18 to 70 (inclusive) [+3]

Symptomatic renal or liver disease, uncontrolled diabetes or thyroid disorder, o... [+12]

Status: Not yet recruiting

Sacituzumab Tirumotecan in Pts w/ NEPC After Progression on Prior Chemotherapy

This is a phase 2, open-label, single-arm study of sacituzumab tirumotecan in neuroendocrine prostate cancer (NEPC) with progression after platinum-based chemotherapy.

Participants needed: 20
Trial details
Phase: Phase 2Age: 18+Biological sex: MaleType: InterventionalSponsor: Virginia Commonwealth UniversityUpdated: Jun 10, 2026Locations: 1
Eligibility criteria

Patients with histologically or cytologically confirmed diagnosis of de novo (d-... [+26]

Has a history of documented severe dry eye syndrome, severe Meibomian gland dise... [+18]