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                    Oklahoma City, OK Paid Clinical Trials
A listing of 672  clinical trials  in Oklahoma City, OK  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            661 - 672 of 672
        
                There are currently 672 clinical trials in Oklahoma City, Oklahoma looking for participants to engage in research studies. Trials are conducted at various facilities, including University of Oklahoma Health Sciences Center, Mercy Hospital Oklahoma City, GSK Investigational Site and Lynn Health Science Institute. Whether you're a healthy volunteer looking to participate in paid medical research or seeking trials related to a specific condition, the city provides a diverse range of opportunities near you. 
            
                                        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)
                    
                                    Featured Trial
                
                Cardiovascular Disease Clinical Study
            
        Recruiting
            
        A clinical study for people that suffer with Cardiovascular Disease
    
    
                            Conditions: 
                                    
        
            
                        Cardiovascular Disease
                    
                                    
                
                                    Effects of Exoskeleton-Assisted Gait Training on Functional Rehabilitation Outcomes in Patients With Stroke
                                
            
            
        Recruiting
                            
            
                The goal of this study is to determine the efficacy of electromechanical exoskeleton-assisted gait training on rehabilitation functional outcomes in patients with stroke undergoing therapy in an in-patient rehabilitation facility.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 90 years
            Trial Updated:
                11/29/2023
            
            Locations: Oklahoma City VA Health Care System, Oklahoma City, Oklahoma         
        
        
            Conditions: Stroke, Weakness of Extremities as Sequela of Stroke
        
            
        
    
                
                                    Screening for Atrial Fibrillation in Patients With Cancer: A Pilot Randomized Controlled Clinical Trial
                                
            
            
        Recruiting
                            
            
                Patients with cancer have a higher incidence of AF but despite the higher incidence of AF in the cancer population, there are no randomized controlled trials (RCTs) for AF screening in this population. RCTs of AF screening in the general population have shown that screening can effectively detect AF earlier, and helps to identify candidates for appropriate anticoagulation that may lead to improvement in clinical outcomes.             
        
        
    Gender:
                ALL
            Ages:
                Between 65 years and 90 years
            Trial Updated:
                11/20/2023
            
            Locations: University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma         
        
        
            Conditions: Cancer
        
            
        
    
                
                                    Genotype and Phenotype Correlation in Hereditary Thrombotic Thrombocytopenic Purpura (Upshaw-Schulman Syndrome)
                                
            
            
        Recruiting
                            
            
                Hereditary thrombotic thrombocytopenic purpura (Upshaw-Schulman syndrome) is a rare disorder characterized by thrombocytopenia as a result of platelet consumption, microangiopathic hemolytic anemia, occlusion of the microvasculature with von Willebrand factor-platelet-thrombic and ischemic end organ damage. The underlying patho-mechanism is a severe congenital ADAMTS13 (a disintegrin and metalloproteinase with thrombospondin type 1 motif, 13) deficiency which is the result of compound heterozygo...  Read More             
        
        
    Gender:
                ALL
            Ages:
                All
            Trial Updated:
                10/10/2023
            
            Locations: University of Oklahoma Health Sciences Center, Department of Medicine, PO Box 26901, Oklahoma City, Oklahoma         
        
        
            Conditions: Thrombotic Thrombocytopenic Purpura, Congenital Thrombotic Thrombocytopenic Purpura, Familial Thrombotic Thrombocytopenic Purpura, Thrombotic Thrombocytopenic Purpura, Congenital, Upshaw-Schulman Syndrome
        
            
        
    
                
                                    CAN-Stim Compared to SNS in Treatment of Urinary Urgency Incontinence With Wireless Neuromodulation Technology
                                
            
            
        Recruiting
                            
            
                This is a prospective, randomized, controlled, multi-center, study in which 150 evaluable subjects will be randomized 1:1 to receive either a Protect CAN-Stim or SNS InterStim® system. Subjects from both groups will immediately start with therapy. The primary endpoint is a ≥ 50% reduction in number of incontinence episodes associated with urgency at the 3-month visit, with additional measurements assessed at 14 days, 1, 6, 9 and 12-months.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                10/03/2023
            
            Locations: University of Oklahoma health Sciences Center, Oklahoma City, Oklahoma         
        
        
            Conditions: Urinary Incontinence, Urge
        
            
        
    
                
                                    A Phase 1/2, Open-label, Multicenter, Dose Escalation and Expansion Study of SLC-3010 Monotherapy and in Combination
                                
            
            
        Recruiting
                            
            
                This is a Phase 1/2, open-label, multicenter, dose escalation and expansion study, evaluating the safety, tolerability, pharmacokinetic, preliminary anti-tumor activity, and effects on pharmacodynamic markers following administration of SLC-3010 as monotherapy and in combination with gemcitabine, in patients with various advanced solid tumors.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                09/18/2023
            
            Locations: Selecxine Investigator site, Oklahoma City, Oklahoma         
        
        
            Conditions: Advanced Solid Tumor
        
            
        
    
                
                                    A Phase 3 Study to Investigate the Efficacy and Safety of SHR0302 With Moderately to Severely Active Ulcerative Colitis
                                
            
            
        Recruiting
                            
            
                This is a randomized, double-blind, placebo-controlled, multicenter Phase 3 study that will enroll approximately 368 subjects aged 18 to 75 years old with Moderately to Severely Active Ulcerative Colitis.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                09/01/2023
            
            Locations: DDSI, Oklahoma City, Oklahoma  +1 locations         
        
        
            Conditions: Ulcerative Colitis
        
            
        
    
                
                                    AltaValve Early Feasibility Study Protocol
                                
            
            
        Recruiting
                            
            
                Prospective, single-arm, multicenter study to evaluate the safety and performance of the AltaValve for the treatment of moderate to severe or severe mitral valve regurgitation in subjects who are considered high risk for mortality and morbidity from conventional open-heart surgery.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                08/31/2023
            
            Locations: Oklahoma Heart Hospital, Oklahoma City, Oklahoma         
        
        
            Conditions: Mitral Regurgitation, Mitral Insufficiency, Mitral Valve Incompetence, Mitral Valve Regurgitation, Mitral Incompetence
        
            
        
    
                
                                    Groningen International Study on Sentinel Nodes in Vulvar Cancer-III
                                
            
            
        Recruiting
                            
            
                Vulvar cancer patients with SN-metastasis \> 2mm will receive chemoradiation instead of an inguinofemoral lymphadenectomy.             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                07/27/2023
            
            Locations: University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma         
        
        
            Conditions: Vulvar Cancer, Sentinel Lymph Node, Lymph Node Metastases
        
            
        
    
                
                                    Physica System Total Knee Replacement Registry Study
                                
            
            
        Recruiting
                            
            
                The primary objective of this study is to obtain long-term implant survivorship (out to 10 years) and to assess clinical, patient-reported outcome measures, and radiographic data for the commercially available Physica system. For ancillary arm, from baseline to 5-year follow-up.             
        
        
    Gender:
                ALL
            Ages:
                22 years and above
            Trial Updated:
                03/17/2023
            
            Locations: Joint Reconstructive Specialist, Oklahoma City, Oklahoma         
        
        
            Conditions: Osteoarthritis, Knee, Traumatic Arthritis, Avascular Necrosis, Degenerative Joint Disease of Knee, Rheumatoid Arthritis, Deformity of Knee
        
            
        
    
                
                                    Study to Assess Allogeneic Anti-CD38 A2 Dimeric Antigen Receptor T Cells in Relapsed or Refractory Multiple Myeloma
                                
            
            
        Recruiting
                            
            
                This is a phase 1b, open-label, dose-escalation study of STI-1492 administered by a single intravenous infusion in subjects with relapsed or refractory multiple myeloma.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                01/12/2023
            
            Locations: University of Oklahoma, Oklahoma City, Oklahoma         
        
        
            Conditions: Multiple Myeloma
        
            
        
    
                
                                    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, Oklahoma City, Oklahoma         
        
        
            Conditions: Ulcerative Colitis
        
            
        
    
                
                                    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: Sooner Clinical Research, Oklahoma City, Oklahoma         
        
        
            Conditions: Schizophrenia
        
            
        
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