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                    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.
            2245 - 2256 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
                
                Ischemic heart disease (IHD) Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Ischemic heart disease (IHD)
    
    
                            Conditions: 
                                    
        
            
                        Ischemic heart disease (IHD)
                    
                                    
                
                                    A Multicenter Patient Registry on Outcomes From Cryoanalgesia of the Intercostal Nerves
                                
            
            
        Recruiting
                            
            
                This is a retrospective and prospective, multicenter, observational patient registry to record outcomes from patients undergoing cryoablation of the intercostal nerves (cryoanalgesia) for post-operative pain management.             
        
        
    Gender:
                ALL
            Ages:
                12 years and above
            Trial Updated:
                03/18/2025
            
            Locations: The Christ Hospital, Cincinnati, Ohio         
        
        
            Conditions: Post Operative Pain
        
            
        
    
                
                                    A Safety and Dose-finding Study of PRL-02 Depot in Men With Advanced Prostate Cancer
                                
            
            
        Recruiting
                            
            
                Medicines that reduce the amount of testosterone in the body are commonly used to treat prostate cancer. PRL-02 depot is a potential treatment for men with advanced prostate cancer. It is given by an injection into the muscle. Men with advanced prostate cancer can take part in this study. Their cancer has come back after previous cancer treatment, or the previous cancer treatment they had didn't work.
The main aims of the study are:
* to check the safety of PRL-02 depot given with and without...  Read More             
        
        
    Gender:
                MALE
            Ages:
                18 years and above
            Trial Updated:
                03/18/2025
            
            Locations: Helios Clinical Research, LLC, Middleburg Heights, Ohio         
        
        
            Conditions: Prostate Cancer, Metastatic Castration Resistant Prostate Cancer, Metastatic Castration-sensitive Prostate Cancer
        
            
        
    
                
                                    CI Following VS Removal or Labyrinthectomy
                                
            
            
        Recruiting
                            
            
                This study is a prospective, clinical study to determine if it is safe and effective to use a cochlear implant over time in individuals undergoing removal of a vestibular schwannoma (VS), benign tumor of the hearing and balance nerve or undergoing a labyrinthectomy for treatment of Meniere's disease. Individuals undergoing these surgeries will be deaf on the surgical side after the procedure. Currently, cochlear implants are approved for use and not considered investigational in individuals with...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 70 years
            Trial Updated:
                03/18/2025
            
            Locations: The Ohio State University, Columbus, Ohio         
        
        
            Conditions: Vestibular Schwannoma, Meniere Disease
        
            
        
    
                
                                    EEG-based Personalized Transcranial Magnetic Stimulation (eTMS) to Treat Post-Traumatic Stress Disorder
                                
            
            
        Recruiting
                            
            
                This is a randomized, sham controlled study of the Electroencephalogram (EEG) based Transcranial Magnetic Stimulation (eTMS) treatment for Post-Traumatic Stress Disorder (PTSD). The recruitment goal is 110 participants who are United States Military veterans or first responders (e.g., firefighters, police, paramedics, etc.). The Study includes an EEG recording in order to determine the optimal treatment parameters for the eTMS system, followed by 15 in-office visits that take place over 21-28 to...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 22 years and 65 years
            Trial Updated:
                03/17/2025
            
            Locations: Wright State University, Dayton, Ohio         
        
        
            Conditions: Stress Disorder, Post Traumatic
        
            
        
    
                
                                    Early Assessment and Initiation of GuideLine-Directed Evidence-Based Management-HF
                                
            
            
        Recruiting
                            
            
                EAGLE-HF (Early Assessment and initiation of GuideLine-directed Evidence-based management-HF) is a prospective single site study of a multinational, unblinded, randomized-controlled, longitudinal trial called SYMPHONY. Primary, secondary and exploratory outcomes that are part of SYMPHONY are not described herein as they replicate SYMPHONY outcomes. Data associated with SYMPHONY outcomes will be sent to the SYMPHONY coordinating center. In EAGLE-HF, site investigators will examine if a new-onset...  Read More             
        
        
    Gender:
                ALL
            Ages:
                40 years and above
            Trial Updated:
                03/17/2025
            
            Locations: Cleveland Clinic, Cleveland, Ohio         
        
        
            Conditions: Heart Failure, Socioeconomic Adversity
        
            
        
    
                
                                    Assessment of Biomarker-Guided CNI Substitution In Kidney Transplantation
                                
            
            
        Recruiting
                            
            
                800 adult first time kidney transplant recipients will be enrolled in the Observational Study and followed to evaluate their Human Leukocyte Antigen (HLA)-DR/DQ molecular mismatch (mMM) score as a risk-stratifying prognostic biomarker. Six months after transplant the study will identify those who meet the eligibility criteria for the Nested Randomized Control Trial (RCT). 300 eligible subjects will be randomized 2:1 to abatacept or Standard of care (SOC) in the randomization and followed for 18...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 70 years
            Trial Updated:
                03/17/2025
            
            Locations: Cleveland Clinic Foundation: Transplantation, Cleveland, Ohio         
        
        
            Conditions: Kidney Transplant
        
            
        
    
                
                                    Comparison of Anti-coagulation and Anti-Platelet Therapies for Intracranial Vascular Atherostenosis- Magnetic Resonance Imaging
                                
            
            
        Recruiting
                            
            
                CAPTIVA-MRI is an observational multimodal MR imaging study that is ancillary to the CAPTIVA trial \[a 3-arm, double-blind Phase III trial conducted at approximately 115 StrokeNet sites randomizing patients with stroke attributed to 70-99% intracranial atherosclerotic stenosis (ICAS) to aspirin plus ticagrelor, clopidogrel, or rivaroxaban.\] The primary goal of this ancillary study is to determine if MRI biomarkers can potentially identify ICAS patients who fail best medical management. The CAPT...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                03/17/2025
            
            Locations: UH Cleveland Medical Center, Cleveland, Ohio         
        
        
            Conditions: Stroke, Intracranial Atherosclerotic Stenosis (ICAS)
        
            
        
    
                
                                    Brief Cognitive Behavioral Therapy for People with Physical Disabilities
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to examine the effectiveness of a psychotherapy (non-medication) treatment, Brief Cognitive Behavioral Therapy for Suicide Prevention, in reducing suicide ideation and attempts for people with physical disabilities.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                03/17/2025
            
            Locations: The Ohio State Universitty Wexner Medical Center, Columbus, Ohio         
        
        
            Conditions: Suicide, Suicide, Attempted, Suicidal Ideation, Disability Physical, Disability Hearing, Disability, Vision
        
            
        
    
                
                                    Effect of Moderate Renal Impairment and Race/Ethnicity on Treosulfan Pharmacokinetics
                                
            
            
        Recruiting
                            
            
                This study aim is to assess, if treosulfan pharmacokinetics are influenced by declined renal function and by race/ethnicity of patients. The study also aims to determine an appropriate safe dose of treosulfan, when patient's renal function is impaired. The participants of this study are undergoing allogenic hematopoietic stem cell transplantation for treatment of acute myeloid leukemia or myelodysplastic syndrome.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                03/17/2025
            
            Locations: The Ohio State University, Columbus, Ohio         
        
        
            Conditions: Acute Myeloid Leukaemia (AML), Myelodysplastic Syndrome (MDS), Allogeneic Hematopoietic Stem Cell Transplantation (HSCT)
        
            
        
    
                
                                    Medtronic Deep Brain Stimulation (DBS) Therapy for Epilepsy Post-Approval Study (EPAS)
                                
            
            
        Recruiting
                            
            
                The purpose of this post-approval study is to further evaluate the long-term safety and effectiveness of Medtronic DBS therapy for epilepsy on seizure reduction in newly implanted participants through 3 years of follow-up.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                03/17/2025
            
            Locations: Cleveland Clinic, Cleveland, Ohio         
        
        
            Conditions: Epilepsy
        
            
        
    
                
                                    International Pediatric Adrenocortical Tumor Registry
                                
            
            
        Recruiting
                            
            
                This study aims to collect demographic and medical information including detailed family history of cancer of children and adolescents with adrenocortical tumors in order to learn more about the clinical and epidemiological aspects, treatment modalities, and outcome of patients with this rare disease, worldwide.
In addition, investigators at St. Jude Children's Research Hospital (SJCRH) plan to perform molecular studies of tumor cells aimed to clarify the role of the TP53 gene and other genetic...  Read More             
        
        
    Gender:
                ALL
            Ages:
                21 years and below
            Trial Updated:
                03/17/2025
            
            Locations: The Children's Medical Center, Dayton, Ohio         
        
        
            Conditions: Adrenocortical Tumor
        
            
        
    
                
                                    Safety and Efficacy of NMD670 in Adult Patients with Type 1 and Type 2 Charcot-Marie-Tooth Disease
                                
            
            
        Recruiting
                            
            
                This Phase 2a study aims to evaluate the efficacy, safety and tolerability of NMD670 vs placebo administered twice a day (BID) for 21 days in ambulatory adult patients with Charcot-Marie-Tooth disease type 1 and type.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 70 years
            Trial Updated:
                03/14/2025
            
            Locations: OSU Department of Neurology Division of Neuromuscular Diseases, Columbus, Ohio         
        
        
            Conditions: Charcot-Marie-Tooth Disease
        
            
        
    