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                    South Carolina Paid Clinical Trials
A listing of 1173  clinical trials  in South Carolina  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            397 - 408 of 1173
        
                South Carolina is currently home to 1173 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Charleston, Greenville, Spartanburg and Columbia. 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.
As a valued user, you’re eligible for $50 off your first program with code policy-lab-50.
    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)
                    
                                    
                
                                    Sleep for Stroke Management and Recovery Trial
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to determine whether treatment of obstructive sleep apnea (OSA) with positive airway pressure starting shortly after acute ischemic stroke (1) reduces recurrent stroke, acute coronary syndrome, and all-cause mortality 6 months after the event, and (2) improves stroke outcomes at 3 months in patients who experienced an ischemic stroke.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/01/2025
            
            Locations: Palmetto Health Richland, Columbia, South Carolina         
        
        
            Conditions: Ischemic Stroke, Sleep Apnea, Sleep Apnea, Obstructive, Stroke, CPAP, Telemedicine, Home Sleep Apnea Test, Randomized Clinical Trial, Multicenter Trial
        
            
        
    
                
                                    A Phase III Study of AZD0780 on Major Adverse CV Events in Patients With a History of ASCVD Events or at High Risk for a First Event
                                
            
            
        Recruiting
                            
            
                The purpose of this phase 3, randomized, placebo controlled, event-driven study is to assess the effect of AZD0780, an oral PCSK9 inhibitor, compared with placebo in reducing the risk of MACE-PLUS in patients with established ASCVD or at high risk for a first ASCVD event. The effect of AZD0780 vs placebo on the risk of MACE-PLUS will be evaluated from randomisation until the primary analysis censoring date (PACD). The Study Closure Visit will be scheduled to occur after the PACD and will be the...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/31/2025
            
            Locations: Research Site, Charleston, South Carolina         
        
        
            Conditions: Cardiovascular Disease
        
            
        
    
                
                                    A Study to Assess the Efficacy and Safety of Verekitug in Participants With COPD
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to assess the efficacy and safety of verekitug (UPB-101) in participants with moderate-to-severe Chronic Obstructive Pulmonary Disease (COPD), an inflammatory lung disease.             
        
        
    Gender:
                ALL
            Ages:
                Between 40 years and 85 years
            Trial Updated:
                07/31/2025
            
            Locations: Velocity Clinical Research, Gaffney, Greenville, South Carolina         
        
        
            Conditions: Chronic Obstructive Pulmonary Disease
        
            
        
    
                
                                    Investigation of Skin Pigmentation Effect on Performance of Masimo Pulse Oximetry (INSPIRE)
                                
            
            
        Recruiting
                            
            
                The objective of this study is to evaluate the performance of Masimo RD SET® SpO2 sensors in subjects with light and dark skin pigmentation in the intensive care therapeutic area.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 89 years
            Trial Updated:
                07/31/2025
            
            Locations: Medical University of South Carolina, Charleston, South Carolina         
        
        
            Conditions: Hypoxemia
        
            
        
    
                
                                    tFUS Induced Transient Scotoma for Individual Dosing
                                
            
            
        Recruiting
                            
            
                The purposes of this research study is to:
1. Develop a technique of transcranial Focused Ultrasound Stimulation (tFUS) where meaningful effects on the brain can be easily measured.
2. Use this technique to measure threshold for effective tFUS in individuals.
3. Determine whether disruption of conscious visual detection, versus non-conscious visually-guided behavior have different thresholds for disruption with tFUS.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 70 years
            Trial Updated:
                07/31/2025
            
            Locations: Medical University of South Carolina Brain Stimulation Division, Charleston, South Carolina         
        
        
            Conditions: Healthy
        
            
        
    
                
                                    Study to Evaluate the Effect of Balcinrenone/Dapagliflozin in Patients With Heart Failure and Impaired Kidney Function
                                
            
            
        Recruiting
                            
            
                This is a Phase III, international, multi-centre, randomised, double-blind, parallel-group, double-dummy, active-controlled, event-driven study in patients with chronic HF and impaired kidney function who had a recent HF event. The aim is to evaluate the effect of balcinrenone/dapagliflozin vs dapagliflozin, given once daily on top of other classes of SoC, on CV death and HF events.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 130 years
            Trial Updated:
                07/31/2025
            
            Locations: Research Site, Anderson, South Carolina         
        
        
            Conditions: Heart Failure and Impaired Kidney Function
        
            
        
    
                
                                    Cord Clamping Among Neonates With Congenital Heart Disease
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to compare 2 different timepoints for clamping the umbilical cord at birth for term-born infants with a prenatal diagnosis of congenital heart disease (CHD). The main questions it aims to answer are:
* Does Delayed Cord Clamping at 120 seconds (DCC-120) or Delayed Cord Clamping at 30 seconds (DCC-30) after birth lead to better health outcomes?
* Does DCC-120 seconds or DCC-30 seconds after birth lead to better neuromotor outcomes at 22-26 months of infant age...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 37 weeks and 42 weeks
            Trial Updated:
                07/31/2025
            
            Locations: Medical University of South Carolina, Columbia, South Carolina         
        
        
            Conditions: Congenital Heart Disease (CHD)
        
            
        
    
                
                                    Registry of the Patient Experience for Carpal Tunnel Release
                                
            
            
        Recruiting
                            
            
                Multi-center study to collect large scale, multidimensional real-world data on patients undergoing carpal tunnel release (CTR).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/31/2025
            
            Locations: Ortho SC (CTR-US), Conway, South Carolina         
        
        
            Conditions: Carpal Tunnel Syndrome, CTS
        
            
        
    
                
                                    Study Evaluating INS018_055 Administered Orally to Subjects With Idiopathic Pulmonary Fibrosis
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to learn about INS018_055 in adults with Idiopathic Pulmonary Fibrosis (IPF).
The primary objective is to evaluate the safety and tolerability of INS018_055 orally administered for up to 12 weeks in adult subjects with IPF compared to placebo.             
        
        
    Gender:
                ALL
            Ages:
                40 years and above
            Trial Updated:
                07/31/2025
            
            Locations: Bogan Sleep Consultants, LLC, Columbia, South Carolina         
        
        
            Conditions: Idiopathic Pulmonary Fibrosis (IPF)
        
            
        
    
                
                                    Novel Cellular Therapy for the Treatment of Pain Associated With Chronic Pancreatitis
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to test whether adult stem cells, called mesenchymal stem cells (MSCs) collected from the patient's bone marrow can help reduce pain caused by chronic pancreatitis and improve pancreatic function.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                07/31/2025
            
            Locations: Ralph H. Johnson VA Medical Center, Charleston, SC, Charleston, South Carolina         
        
        
            Conditions: Chronic Pancreatitis, Chronic Pain
        
            
        
    
                
                                    Long-term, Open-label Study of SAR447537 (INBRX-101) in Adults With Alpha-1 Antitrypsin Deficiency Emphysema
                                
            
            
        Recruiting
                            
            
                Phase 2 open label extension study to evaluate SAR447537 (INBRX-101) in adults with AATD emphysema             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                07/31/2025
            
            Locations: Velocity Clinical Research - Spartanburg - PPDS- Site Number : 120, Spartanburg, South Carolina         
        
        
            Conditions: Alpha 1-Antitrypsin Deficiency, Emphysema
        
            
        
    
                
                                    Study to Evaluate Safety, Efficacy and Pharmacokinetics (PK) of a Modified Regimen of Ublituximab
                                
            
            
        Recruiting
                            
            
                The primary purpose of this phase 3b study is to assess the efficacy of a modified regimen of ublituximab as measured by T1 Gadolinium (Gd)-enhancing lesions and pharmacokinetics in participants with Relapsing Multiple Sclerosis (RMS). The study consists of 2 parts: Part A is single-armed and open-label and Part B is randomized, double-blind, placebo-controlled.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 65 years
            Trial Updated:
                07/31/2025
            
            Locations: TG Therapeutics Investigational Trial Site, Greenville, South Carolina         
        
        
            Conditions: Relapsing Multiple Sclerosis
        
            
        
    