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                    Virginia Paid Clinical Trials
A listing of 1861  clinical trials  in Virginia  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            1537 - 1548 of 1861
        
                Virginia is currently home to 1861 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Richmond, Charlottesville, Norfolk and Fairfax. Whether you're a healthy volunteer interested in paid medical research or someone seeking trials related to a specific condition, the state offers a diverse array of opportunities in your vicinity.
            
                                                Featured Trial
                
                Healthy Participants Needed (Colonoscopy + Cancer Screening)
            
        Recruiting
            
        Earn $325 - $475 in electronic payment card compensation for your time and effort by participating in a clinical study to develop a blood test that may one day help screen for colon cancer. Take a quick quiz to see if you qualify.
    
    
                            Conditions: 
                                    
        
            
                        Healthy
                    
                                    
                        Healthy Volunteers
                    
                                    
                        Healthy Subjects
                    
                                    
                        Healthy Volunteer
                    
                                    
                        Healthy Participants
                    
                                    Featured Offer
                
                Lose Weight with GLP-1 Medications
            
        Recruiting
            
        Policy Lab has partnered with OnlineSemaglutide.org to offer trusted access to semaglutide and other GLP-1 medications, including generic alternatives to Ozempic® and Wegovy®. 
GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
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    GLP-1 medications are scientifically backed to help individuals achieve significant weight loss—on average, 15-20% of body weight within a year.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
                            Conditions: 
                                    
        
            
                        Overweight
                    
                                    
                        Overweight and Obesity
                    
                                    
                        Obesity
                    
                                    
                        Weight Loss
                    
                                    
                        Morbid Obesity
                    
                                    Featured Trial
                
                Stroke Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Stroke
    
    
                            Conditions: 
                                    
        
            
                        Stroke
                    
                                    Featured Trial
                
                Chronic Kidney Disease (CKD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Chronic Kidney Disease (CKD)
    
    
                            Conditions: 
                                    
        
            
                        Chronic Kidney Disease (CKD)
                    
                                    Featured Trial
                
                Ischemic heart disease (IHD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Ischemic heart disease (IHD)
    
    
                            Conditions: 
                                    
        
            
                        Ischemic heart disease (IHD)
                    
                                    
                
                                    Low-Intensity Focused Ultrasound and the Complex Patient
                                
            
            
        Recruiting
                            
            
                Studying the effects of Low Intensity Focused Ultrasound (LIFU) on measures of pain, craving, and anxiety in a complex patient population.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 65 years
            Trial Updated:
                01/09/2025
            
            Locations: Fralin Biomedical Research Institute at VTC, Roanoke, Virginia         
        
        
            Conditions: Opioid Use Disorder, Chronic Pain, Anxiety Disorder
        
            
        
    
                
                                    BEETroot Juice to Reverse Functional Impairment in PAD
                                
            
            
        Recruiting
                            
            
                The BEET PAD Trial is a multi-centered double-blind randomized clinical trial designed to determine whether beetroot juice, compared to placebo, improves six-minute walk distance at four month follow-up in people with lower extremity peripheral artery disease (PAD). Investigators hypothesize that by simultaneously increasing lower extremity perfusion, gastrocnemius muscle mitochondrial activity, and myofiber health and regeneration, beetroot juice will significantly improve walking performance i...  Read More             
        
        
    Gender:
                ALL
            Ages:
                50 years and above
            Trial Updated:
                01/09/2025
            
            Locations: University of Virginia, Charlottesville, Virginia         
        
        
            Conditions: Peripheral Artery Disease
        
            
        
    
                
                                    The Role of Loteprednol in Reducing Post-Intravitreal Injection Related Pain
                                
            
            
        Recruiting
                            
            
                Patients are already receiving an intravitreal injection as a standard of care, but they are consenting to receiving a loteprednol drop following the intravitreal injection. This clinical trial is studying the role of loteprednol (corticosteroid) in reducing pain following intravitreal injections for patients with age-related macular degeneration. As of now, there is no definitive pain management technique following intravitreal injections. Loteprednol is a corticosteroid widely used in ophthalm...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/09/2025
            
            Locations: Vistar Eye Center, Roanoke, Virginia         
        
        
            Conditions: Age-Related Macular Degeneration
        
            
        
    
                
                                    Study of INBRX-109 in Conventional Chondrosarcoma
                                
            
            
        Recruiting
                            
            
                Randomized, blinded, placebo-controlled, Phase 2 study of INBRX-109 in unresectable or metastatic conventional chondrosarcoma patients.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 85 years
            Trial Updated:
                01/09/2025
            
            Locations: Virginia Cancer Specialists, Fairfax, Virginia         
        
        
            Conditions: Conventional Chondrosarcoma
        
            
        
    
                
                                    T-DM1 and Tucatinib Compared with T-DM1 Alone in Preventing Relapses in People with High Risk HER2-Positive Breast Cancer, the CompassHER2 RD Trial
                                
            
            
        Recruiting
                            
            
                This phase III trial studies how well trastuzumab emtansine (T-DM1) and tucatinib work in preventing breast cancer from coming back (relapsing) in patients with high risk, HER2 positive breast cancer. T-DM1 is a monoclonal antibody, called trastuzumab, linked to a chemotherapy drug, called DM1. Trastuzumab is a form of targeted therapy because it attaches to specific molecules (receptors) on the surface of cancer cells, known as HER2 receptors, and delivers DM1 to kill them. Tucatinib may stop t...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/09/2025
            
            Locations: Wellmont Medical Associates-Bristol, Bristol, Virginia         
        
        
            Conditions: Anatomic Stage IA Breast Cancer AJCC v8, Anatomic Stage II Breast Cancer AJCC v8, Anatomic Stage IIA Breast Cancer AJCC v8, Anatomic Stage IIB Breast Cancer AJCC v8, Anatomic Stage III Breast Cancer AJCC v8, Anatomic Stage IIIA Breast Cancer AJCC v8, Anatomic Stage IIIB Breast Cancer AJCC v8, Anatomic Stage IIIC Breast Cancer AJCC v8, HER2 Positive Breast Carcinoma, Invasive Breast Carcinoma, Multifocal Breast Carcinoma, Prognostic Stage I Breast Cancer AJCC v8, Prognostic Stage IA Breast Cancer AJCC v8, Prognostic Stage IB Breast Cancer AJCC v8, Prognostic Stage II Breast Cancer AJCC v8, Prognostic Stage IIA Breast Cancer AJCC v8, Prognostic Stage IIB Breast Cancer AJCC v8, Prognostic Stage III Breast Cancer AJCC v8, Prognostic Stage IIIA Breast Cancer AJCC v8, Prognostic Stage IIIB Breast Cancer AJCC v8, Prognostic Stage IIIC Breast Cancer AJCC v8, Synchronous Bilateral Breast Carcinoma
        
            
        
    
                
                                    Clinical Trial Evaluating an Amnion Membrane Allograft for Use in the Management of Non- Healing Diabetic Foot Ulcers Versus Standard Of Care
                                
            
            
        Recruiting
                            
            
                The main purpose of this research study is to compare the proportion of wound closure in subjects that receive E-GRAFT™ with Standard of Care (SOC) versus FIBRACOL™ with SOC. Other research purposes include the following:
* Rate of wound closure
* Change in ulcer size over 12 weeks
* Any adverse events or reactions (side effects)
* Changes in neuropathy (nerve damage)
* Change in pain levels
* Occurrence of infection             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/08/2025
            
            Locations: Professional Education and Research Institute, Roanoke, Virginia         
        
        
            Conditions: Diabetic Foot Ulcers (DFUs)
        
            
        
    
                
                                    Effectiveness of Adding Morphine to Intraosseous Vancomycin for Pain Control in Total Knee Arthroplasty
                                
            
            
        Recruiting
                            
            
                Study investigators propose to investigate if a bony injection of pain medication during a knee replacement will help pain levels following primary knee replacement surgery. To investigate this, 86 patients will be enrolled. Half of the patients will receive a bony injection of antibiotics with morphine (pain medication) while the other half will receive a bony injection of antibiotics with placebo (no pain medication). Following surgery, patient pain levels and pain medication consumption will...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 100 years
            Trial Updated:
                01/08/2025
            
            Locations: Carilion Clinic, Roanoke, Virginia         
        
        
            Conditions: Primary Total Knee Arthroplasty, Intraosseous Morphine Injection, Knee Osteoarthritis
        
            
        
    
                
                                    Phase I/II Study of SKG0106 Intravitreal Injection in Patients With Neovascular Age-related Macular Degeneration (nAMD)
                                
            
            
        Recruiting
                            
            
                This is a phase 1/2 clinical study to evaluate the safety, preliminary efficacy, immunogenicity, and pharmacokinetic (PK) characteristics of SKG0106 in subjects with nAMD. Based on results from the phase 1 dose escalation study, the phase 2 expansion study will be conducted.             
        
        
    Gender:
                ALL
            Ages:
                50 years and above
            Trial Updated:
                01/08/2025
            
            Locations: Wagner Kapoor Research Institute, Norfolk, Virginia         
        
        
            Conditions: Neovascular Age-related Macular Degeneration
        
            
        
    
                
                                    Neuroscience-informed Treatment to Remotely Target Reward Mechanisms in Post-acute Anorexia Nervosa
                                
            
            
        Recruiting
                            
            
                The investigators will recruit individuals with broadly-defined AN (n = 80) who are currently in or have recently participated in higher-level eating disorder treatment (e.g., residential, partial hospitalization/day treatment, intensive outpatient treatment). Interested participants will sign consent, complete eligibility assessments, and will be randomized to receive Positive Affect Treatment for Anorexia Nervosa (PAT-AN) or Psychoeducation and Behavioral Therapy (PBT) through teletherapy shor...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/08/2025
            
            Locations: Virginia Commonwealth University, Richmond, Virginia         
        
        
            Conditions: Anorexia Nervosa
        
            
        
    
                
                                    Clinical Trial Evaluating an Amnion Membrane Allograft Intended for Use in the Management of Non- Healing Venous Leg Ulcers Versus Standard Of Care Alone
                                
            
            
        Recruiting
                            
            
                The main purpose of this research study is to compare the proportion of wound closure in subjects that receive E-GRAFT™ with SOC versus FIBRACOL™ with SOC. Other research purposes include the following:
* Rate of wound closure
* Change in ulcer size over 12 weeks
* Any adverse events or reactions (side effects)
* Change in pain levels
* Occurrence of infection             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/07/2025
            
            Locations: Professional Education and Research Institute, Roanoke, Virginia         
        
        
            Conditions: Venous Leg Ulcers
        
            
        
    
                
                                    Post Approval Study Investigating Lutonix Drug Coated Balloon for Treatment of Dysfunctional Arteriovenous Fistulae
                                
            
            
        Recruiting
                            
            
                This prospective, global, multicenter, single arm post-approval study is designed to investigate the clinical use and safety of the Lutonix® 035 AV Drug Coated Balloon (DCB) PTA Catheter in subjects presenting with clinical and hemodynamic abnormalities in native arteriovenous (AV) fistulae located in the upper extremity.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/06/2025
            
            Locations: Sentara Medical Group, Norfolk, Virginia         
        
        
            Conditions: Arteriovenous Fistula
        
            
        
    
                
                                    A Study of OR502, a Monoclonal Antibody Targeting LILRB2, Alone and in Combination With Anticancer Agents
                                
            
            
        Recruiting
                            
            
                This is an open-label, multicenter, first-in-human dose-escalation and expansion Phase 1-2 study designed to determine the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary anti-tumor activity of OR502 administered as a monotherapy and in combination with cemiplimab in subjects with advanced solid tumors.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/03/2025
            
            Locations: NEXT Virginia, Fairfax, Virginia         
        
        
            Conditions: Cancer, Tumor, Solid, Malignant Neoplasm, Metastatic Cancer, Advanced Solid Tumor, Cutaneous Melanoma, Non-small Cell Lung Cancer
        
            
        
    