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                    North Carolina Paid Clinical Trials
A listing of 2641  clinical trials  in North Carolina  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            2629 - 2640 of 2641
        
                North Carolina is currently home to 2641 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Durham, Charlotte, Winston-Salem and Chapel Hill. 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)
                    
                                    
                
                                    Physiologic Signals and Signatures With the Accuryn Monitoring System - The Accuryn Registry
                                
            
            
        Recruiting
                            
            
                The Accuryn Registry Study is an open-ended, global, multi-center, retrospective and prospective, single-arm data collection study with an FDA cleared device. The target population are cardiovascular surgery patients. Physiologic data measurements will be collected from enrolled subjects using electronic medical records and data streams via the Accuryn Monitoring System.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                09/26/2022
            
            Locations: Mission Health Hospital, Asheville, North Carolina         
        
        
            Conditions: Intraabdominal Hypertension, Abdominal Compartment Syndrome, Acute Kidney Injury, Cardiovascular Surgery
        
            
        
    
                
                                    Gedatolisib Plus Fulvestrant With or Without Palbociclib vs Standard-of-Care for the Treatment of Patients With Advanced or Metastatic HR+/HER2- Breast Cancer
                                
            
            
        Recruiting
                            
            
                This is a Phase 3, open-label, randomized, clinical trial evaluating the efficacy and safety of gedatolisib plus fulvestrant with or without palbociclib for the treatment of patients with locally advanced or metastatic HR+/HER2- breast cancer following progression on or after CDK4/6 and aromatase inhibitor therapy.
Condition or disease:
Breast Cancer
Intervention/treatment:
Drug: Gedatolisib
Drug: Palbociclib
Drug: Fulvestrant
Drug: Alpelisib
Phase 3             
        
        
    Gender:
                All
            Ages:
                18 years and above
            Trial Updated:
                08/02/2022
            
            Locations: Cone Health Cancer Center at Alamance Regional, Hematology/Oncology, Greensboro, North Carolina         
        
        
            Conditions: Breast Cancer
        
            
        
    
                
                                    USCRI READY4Life Program
                                
            
            
        Recruiting
                            
            
                The U.S. Committee for Refugees and Immigrants (USCRI) has developed the Relationships, Education, Advancement, and Development for Youth for Life (READY4Life) Program. This is a 16-hour program for immigrants/refugees, ages 14 to 24. The program is designed to help young immigrants and refugees prepare for a successful life in the United States. The program is taught by USCRI program staff and is being implemented at eight sites across the U.S.: Cleveland, Ohio; Colchester, Vermont; Des Moines,...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 14 years and 24 years
            Trial Updated:
                07/27/2022
            
            Locations: USCRI North Carolina, Raleigh, North Carolina         
        
        
            Conditions: Communication, Problem Solving, Social Relationships, Economic Stability
        
            
        
    
                
                                    Introducing Palliative Care (PC) Within the Treatment of End Stage Liver Disease (ESLD)
                                
            
            
        Recruiting
                            
            
                This is a comparative effectiveness study of two pragmatic models aiming to introduce palliative care for end stage liver disease patients. The 2 comparators are:
Model 1: Consultative Palliative Care (i.e. direct access to Palliative Care provider), Model 2: Trained Hepatologist- led PC intervention (i.e. a hepatologist will receive formal training to deliver Palliative Care services)
Primary Outcome: The change in quality of life from baseline to 3 months post enrollment as assessed by FACT-...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 120 years
            Trial Updated:
                04/05/2022
            
            Locations: UNC Liver Center, Chapel Hill, North Carolina         
        
        
            Conditions: End Stage Liver Disease
        
            
        
    
                
                                    Analysis and Suppression of Tremor During Grasp Using Ultrasound Imaging and Electrical Stimulation
                                
            
            
        Recruiting
                            
            
                Individuals experiencing tremors face difficulty performing activities of daily living caused by involuntary oscillation of the muscles in the hands and arms. Current solutions to help suppress tremors include medication, surgery, assistive devices and lifestyle change. However, each of these has a drawback of its own including cost and unwanted side effects. Aside from the solutions listed, it has been shown that functional electrical stimulation(FES) is a possible solution to help suppress tre...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 90 years
            Trial Updated:
                03/25/2022
            
            Locations: Engineering Building III, Raleigh, North Carolina         
        
        
            Conditions: Parkinson Disease, Essential Tremor
        
            
        
    
                
                                    Study of Acalabrutinib (ACP-196) in Combination With Venetoclax (ABT-199), With and Without Obinutuzumab (GA101) Versus Chemoimmunotherapy for Previously Untreated CLL
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to evaluate the efficacy and safety of acalabrutinib in combination with venetoclax and acalabrutinib in combination with venetoclax with and without obinutuzumab compared to chemoimmunotherapy in subjects with previously untreated CLL.             
        
        
    Gender:
                All
            Ages:
                Between 18 years and 130 years
            Trial Updated:
                01/14/2022
            
            Locations: Research Site, Charlotte, North Carolina         
        
        
            Conditions: Chronic Lymphocytic Leukemia
        
            
        
    
                
                                    Antiretroviral Pregnancy Registry (APR)-Risk of Birth Defects
                                
            
            
        Recruiting
                            
            
                The APR began as the 'Zidovudine in pregnancy Registry' in January 1989 and became the 'Antiretroviral Pregnancy Registry' in January, 1993. The purpose of the APR is to detect any major teratogenic effects involving any of the Registry drugs when administered to pregnant HIV positive women. The Registry is intended to provide an early signal of teratogenicity associated with prenatal use of the antiretroviral drugs. The Registry collects data on prenatal exposures to antiretroviral drugs, poten...  Read More             
        
        
    Gender:
                Female
            Ages:
                All
            Trial Updated:
                10/04/2021
            
            Locations: GSK Investigational Site, Wilmington, North Carolina         
        
        
            Conditions: Infection, Human Immunodeficiency Virus, HIV Infections
        
            
        
    
                
                                    An Active and Placebo-Controlled Study of Brazikumab in Participants With Moderately to Severely Active Ulcerative Colitis
                                
            
            
        Recruiting
                            
            
                The present study D5272C00001 (Legacy # 3151-201-008) seeks to evaluate the efficacy and safety of brazikumab versus placebo in patients with moderately to severely active UC and will include assessments of clinical responses as demonstrated by improvement of symptoms and of colonic mucosal appearance as observed on endoscopy.             
        
        
    Gender:
                All
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                01/19/2021
            
            Locations: Research Site, Morehead City, North Carolina         
        
        
            Conditions: Ulcerative Colitis
        
            
        
    
                
                                    Spinal Cord Injury Registry - North American Clinical Trials Network
                                
            
            
        Recruiting
                            
            
                The NACTN Spinal Cord Injury Registry is a network of clinical centers collecting de-identified data from patients admitted through the Emergency Department of a NACTN center at the time of injury with an initial (first time) spinal cord injury (SCI). Information will be collected on the natural history of SCI and course of treatment through the first 12 months from the date of injury or long as medically indicated. Data collected includes imaging information from CT or MRI scans, neurological a...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                09/22/2020
            
            Locations: Duke University, Durham, North Carolina         
        
        
            Conditions: Spinal Cord Injury
        
            
        
    
                
                                    Proton or Photon RT for Retroperitoneal Sarcomas
                                
            
            
        Recruiting
                            
            
                This research study is a Phase I clinical trial. Phase I clinical trials test the safety of an investigational intervention. Phase I studies also try to define the appropriate dose of the investigational therapy to use for further studies. "Investigational" means that the intervention is still being studied and that research doctors are trying to find out more about it.
Retroperitoneal sarcomas are soft tissue tumors located at the far back of the abdomen. Typically, patients with retroperitone...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                09/01/2020
            
            Locations: Duke University, Durham, North Carolina         
        
        
            Conditions: Retroperitoneal Sarcoma
        
            
        
    
                
                                    Clinical Trial Evaluating the Efficacy, Safety, and Tolerability of Cariprazine in a Dose-Reduction Paradigm in the Prevention of Relapse in Patients With Schizophrenia
                                
            
            
        Recruiting
                            
            
                To evaluate the efficacy and safety of cariprazine at a target dose of 4.5 mg/d compared with placebo in prevention of relapse in patients with schizophrenia
To evaluate the efficacy and safety of cariprazine at a target dose of 3.0 mg/d compared with placebo in prevention of relapse in patients with schizophrenia who were initially stabilized on a target dose of 4.5 mg/d             
        
        
    Gender:
                All
            Ages:
                Between 18 years and 64 years
            Trial Updated:
                08/17/2020
            
            Locations: New Hope Clinical Research, Charlotte, North Carolina         
        
        
            Conditions: Schizophrenia
        
            
        
    
                
                                    VENOUS: A Translational Study of Enterococcal Bacteremia
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to assemble a multicenter prospective cohort of patients with enterococcal bloodstream infections (BSIs) to provide data on outcomes of patients with enterococcal BSIs for sample size calculations for future trials, as well as to characterize enterococcal isolates causing BSIs in order to comprehensively dissect the molecular epidemiology of infecting organisms for future studies.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/26/2020
            
            Locations: University of North Carolina, Chapel Hill, North Carolina         
        
        
            Conditions: Enterococcal Bacteremia
        
            
        
    