Search
                    Ohio Paid Clinical Trials
A listing of 3204  clinical trials  in Ohio  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            2269 - 2280 of 3204
        
                Ohio is currently home to 3204 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Cincinnati, Columbus, Cleveland and Dayton. 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
                
                Cardiovascular Disease Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Cardiovascular Disease
    
    
                            Conditions: 
                                    
        
            
                        Cardiovascular Disease
                    
                                    
                
                                    JUPITER 4.0 - Risk Factors for Failure of Isolated Medial Patellofemoral Ligament Reconstruction
                                
            
            
        Recruiting
                            
            
                The goal of this observational study is to learn about the outcomes of medial patellofemoral ligament (MPFL) reconstruction for the treatment of recurrent patellar instability. The main questions it aims to answer are:
* What are the risk factors for recurrent patellar instability after MPFL reconstruction?
* What functional outcomes do patients report after MPFL reconstruction?
Participants undergoing MPFL reconstruction will answer survey questions about their knee and activity level 1 year...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 10 years and 35 years
            Trial Updated:
                03/12/2025
            
            Locations: Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio         
        
        
            Conditions: Patellar Dislocation, Recurrent, Patellar Dislocation, Patellar Instability, Patellofemoral Dislocation, Patellofemoral Joint Dislocation, Patellofemoral Disorder
        
            
        
    
                
                                    Multi-Site Detection of Barrett's Esophagus in Patients Without Chronic GERD Symptoms
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to develop a method to detect Barrett's esophagus in individuals with a new office based diagnostic test. Barrett's esophagus is a condition in which the flat pink lining of the swallowing tube that connects the mouth to the stomach (the esophagus) becomes damaged by acid reflux. The main question it aims to answer is: Can this approach demonstrate efficacy for screening of Barrett's esophagus?
Participants will:
* Participate in a questionnaire.
* Undergo a...  Read More             
        
        
    Gender:
                ALL
            Ages:
                50 years and above
            Trial Updated:
                03/12/2025
            
            Locations: University Hospitals Cleveland Medical Center, Cleveland, Ohio         
        
        
            Conditions: Barrett Esophagus, Gastroesophageal Reflux, Esophageal Adenocarcinoma
        
            
        
    
                
                                    Vulvovaginal Graft-versus-Host Disease: Diagnosis and Microbiome Evaluation
                                
            
            
        Recruiting
                            
            
                The goal of this observational study is to investigate the development of vulvovaginal graft-versus-host- disease (GVHD), an under-reported and under-recognized manifestation of chronic GVHD. This study aims to characterize the vaginal microbiome in participants undergoing allogeneic hematopoietic cell transplantation (HCT). The main questions it aims to answer are:
* Is the vaginal microbiome altered during allogeneic HCT?
* What changes may help researchers understand the development of vulvo...  Read More             
        
        
    Gender:
                FEMALE
            Ages:
                Between 18 years and 70 years
            Trial Updated:
                03/12/2025
            
            Locations: Cleveland Clinic Taussig Cancer Institute, Case Comprehensive Cancer Center, Cleveland, Ohio         
        
        
            Conditions: Graft Vs Host Disease, Vulvovaginal Signs and Symptoms
        
            
        
    
                
                                    Precise and Objective Identification of Bertolotti Syndrome Using Novel Kinematic Biomarkers
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to collect lumbar rotations, velocity, and accelerations, along with pain scores using a novel dynamic VAS device, from twenty (20) Bertolotti Syndrome patients and twenty (20) non-Bertolotti low back pain patients during range-of-motion tasks. The assessments will be analyzed to determine the differences in kinematics and continuous pain scores between Bertolotti patients and non-Bertolotti low back pain patients.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                03/12/2025
            
            Locations: Cleveland Clinic, Cleveland, Ohio         
        
        
            Conditions: Bertolotti's Syndrome, Lower Back Pain
        
            
        
    
                
                                    A Study of Vedolizumab in Children and Teenagers With Ulcerative Colitis or Crohn's Disease
                                
            
            
        Recruiting
                            
            
                The main aim of this study is to learn how the body of a child or teenager with moderately to severely active ulcerative colitis (UC) or Crohn's disease (CD) processes vedolizumab (pharmacokinetics) given just under the skin subcutaneously (SC).
The participants will be treated with vedolizumab for up to 34 weeks.
During the study, participants will visit their study clinic several times.             
        
        
    Gender:
                ALL
            Ages:
                Between 2 years and 17 years
            Trial Updated:
                03/12/2025
            
            Locations: Cleveland Clinic Foundation, Cleveland, Ohio         
        
        
            Conditions: Ulcerative Colitis, Crohn's Disease
        
            
        
    
                
                                    Safety and Efficacy of NMD670 in Ambulatory Adult Patients With Type 3 Spinal Muscular Atrophy
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to evaluate the efficacy, safety, tolerability and pharmacokinetics of NMD670 in the treatment of ambulatory adults with spinal muscular atrophy type 3             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                03/12/2025
            
            Locations: The Ohio State University Wexner Medical Center, Columbus, Ohio         
        
        
            Conditions: Spinal Muscular Atrophy
        
            
        
    
                
                                    Lung-MAP: A Master Screening Protocol for Previously-Treated Non-Small Cell Lung Cancer
                                
            
            
        Recruiting
                            
            
                This screening and multi-sub-study randomized phase II/III trial will establish a method for genomic screening of similar large cancer populations followed by assigning and accruing simultaneously to a multi-sub-study hybrid Master Protocol (Lung-MAP). The type of cancer trait (biomarker) will determine to which sub-study, within this protocol, a participant will be assigned to compare new targeted cancer therapy, designed to block the growth and spread of cancer, or combinations to standard of...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                03/12/2025
            
            Locations: Aultman Alliance Community Hospital, Alliance, Ohio         
        
        
            Conditions: Previously Treated Non-Small Cell Lung Cancer
        
            
        
    
                
                                    Ethanol Induces Skeletal Muscle Autophagy
                                
            
            
        Recruiting
                            
            
                In this study we plan to demonstrate that ethanol induces skeletal muscle autophagy to degrade MAA adducts.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 65 years
            Trial Updated:
                03/12/2025
            
            Locations: Cleveland Clinic, Cleveland, Ohio         
        
        
            Conditions: Alcoholic Liver Disease
        
            
        
    
                
                                    Mechanisms of Malnutrition in Cirrhosis With Portosystemic Shunting
                                
            
            
        Recruiting
                            
            
                Cirrhosis is characterized by loss of muscle as well as fat mass, which increases morbidity and mortality before, during, and after liver transplantation. A common mechanism for the reduced muscle and fat mass in cirrhosis is an increased expression of the TGF (transforming growth factor)beta superfamily member, myostatin, in the muscle and adipose tissue. The present study will examine the expression of myostatin, its receptor and intracellular signaling pathways in the skeletal muscle and mese...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 70 years
            Trial Updated:
                03/12/2025
            
            Locations: Cleveland Clinic Foundation, Cleveland, Ohio         
        
        
            Conditions: Cirrhosis
        
            
        
    
                
                                    Comparing Two Surgical Techniques for Building Up the Bone Where a Dental Implant is to Be Placed
                                
            
            
        Recruiting
                            
            
                The goal of this observational study is to compare two techniques routinely used to increase bone volume in the jaw prior to placing a dental implant, called osseocondensation and osseodensification. The study participants are healthy adults who are planning to get a dental implant. The main questions it aims to answer are:
* Is there a difference in wound closure and soft tissue healing following implant placement using osseocondensation versus osseodensification?
* Is there a difference in bo...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                03/11/2025
            
            Locations: The Ohio State University College of Dentistry, Columbus, Ohio         
        
        
            Conditions: Dental Implant, Sinus Floor Augmentation
        
            
        
    
                
                                    Quantra Point-of-Care Hemostasis Monitoring
                                
            
            
        Recruiting
                            
            
                The investigators will test the hypothesis that utilization of a blood and blood component transfusion algorithm guided by the POC Quantra QPlus System in patients undergoing complex cardiac surgery will reduce RBC, plasma, cryoprecipitate, and platelet transfusion during surgery and the first 12 postoperative hours, compared to standard of care (central laboratory transfusion monitoring at the primary anesthesia provider's discretion).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                03/11/2025
            
            Locations: Cleveland Clinic Foundation, Cleveland, Ohio         
        
        
            Conditions: Bleeding, Hemostatic Disorder
        
            
        
    
                
                                    A Study of CBX 12 in Subjects With Platinum Resistant or Refractory Ovarian Cancer
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to assess the safety, tolerability, and efficacy of CBX-12 in female subjects with platinum resistant or refractory ovarian cancer at 2 doses; 125 mg/m2 every 21 days or 100 mg/m2 every 21 days.             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                03/11/2025
            
            Locations: University Hospitals Seidman Cancer Center, Cleveland, Ohio         
        
        
            Conditions: Platinum-resistant Ovarian Cancer, Refractory Ovarian Carcinoma
        
            
        
    