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                    Overland Park, KS Paid Clinical Trials
A listing of 178  clinical trials  in Overland Park, KS  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            109 - 120 of 178
        
                There are currently 178 clinical trials in Overland Park, Kansas looking for participants to engage in research studies. Trials are conducted at various facilities, including Menorah Medical Center, University of Kansas Cancer Center-Overland Park, Saint Luke's South Hospital and Pfizer Investigational Site. 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
                    
                                    
                
                                    High-Dose Vitamin D Supplementation for ADT-Induced Bone Loss in Older Prostate Cancer Patients
                                
            
            
        Recruiting
                            
            
                This phase III trial tests whether high-dose vitamin D works in treating androgen-deprivation therapy (ADT)-induced bone loss in patients with prostate cancer who are undergoing androgen-deprivation therapy. Vitamins are substances that the body needs to grow and develop normally. Vitamin D helps the body absorb calcium. Calcium is one of the main building blocks of bone. A lack of vitamin D can lead to bone diseases such as osteoporosis or rickets. This trial may help researchers determine if h...  Read More             
        
        
    Gender:
                MALE
            Ages:
                60 years and above
            Trial Updated:
                06/03/2025
            
            Locations: University of Kansas Cancer Center-Overland Park, Overland Park, Kansas         
        
        
            Conditions: Stage I Prostate Cancer AJCC v8, Stage II Prostate Cancer AJCC v8, Stage III Prostate Cancer AJCC v8, Stage IVA Prostate Cancer AJCC v8
        
            
        
    
                
                                    Hydrus® Microstent New Enrollment Post-Approval Study
                                
            
            
        Recruiting
                            
            
                The purpose of this post-approval study is to evaluate the rate of Hydrus Microstent malposition and associated clinical sequelae occurring within 24 months post-operation. Qualified subjects will undergo uncomplicated cataract surgery with placement of a monofocal intraocular lens (IOL), followed by implantation of the Hydrus Microstent.             
        
        
    Gender:
                ALL
            Ages:
                45 years and above
            Trial Updated:
                06/02/2025
            
            Locations: Stiles Eyecare Excellence Cataracts and Glaucoma, Overland Park, Kansas         
        
        
            Conditions: Primary Open Angle Glaucoma
        
            
        
    
                
                                    Study to Assess the Efficacy of Rina-S Compared to Treatment of Investigator's Choice in Participants With Platinum Resistant Ovarian Cancer
                                
            
            
        Recruiting
                            
            
                This phase 3 study will be conducted in different countries all over the world.
The purpose of this study is to compare how well Rina-S works against platinum-resistant ovarian cancer compared to chemotherapy drugs that are already approved and used for platinum-resistant ovarian cancer.
Treatment in this study could be Rina-S or it could be 1 of 4 indicated chemotherapy agents that are considered standard medical care. There is an equal (50:50) chance of getting Rina-S or an approved chemothe...  Read More             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                06/02/2025
            
            Locations: HCA Midwest Health, Overland Park, Kansas         
        
        
            Conditions: Platinum-resistant Ovarian Cancer
        
            
        
    
                
                                    ENA-001 for Opioid Induced Respiratory Depression
                                
            
            
        Recruiting
                            
            
                This study is a Phase I clinical trial to assess the safety, tolerability, and pharmacokinetic (PK) and pharmacodynamic (PD) profiles with single intravenous (IV) and intramuscular (IM) doses of ENA-001.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 55 years
            Trial Updated:
                05/29/2025
            
            Locations: Dr. Vince Clinical Research, Overland Park, Kansas         
        
        
            Conditions: Respiratory Depression
        
            
        
    
                
                                    Evaluation of VX-828 in Healthy Participants and in Participants With Cystic Fibrosis
                                
            
            
        Recruiting
                            
            
                The purpose of the study is to evaluate safety, tolerability, and pharmacokinetics of VX-828 and VX-828 in triple combination (TC) with Tezacaftor (TEZ)/ VX-118 or TEZ/ deutivacaftor (D-IVA) in healthy participants and VX-828 in combination with D-IVA with or without TEZ in participants with cystic fibrosis (CF).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/23/2025
            
            Locations: Altasciences Clinical Kansas, Overland Park, Kansas         
        
        
            Conditions: Cystic Fibrosis
        
            
        
    
                
                                    Evaluate the Safety and Effectiveness of iSTAR Medical's MINIject™ Implant for Lowering Intraocular Pressure (IOP) in Subjects With Primary Open-angle Glaucoma.
                                
            
            
        Recruiting
                            
            
                Evaluate the safety and effectiveness of iSTAR Medical's MINIject™ implant for lowering intraocular pressure (IOP) in subjects with primary open-angle glaucoma.             
        
        
    Gender:
                ALL
            Ages:
                46 years and above
            Trial Updated:
                05/21/2025
            
            Locations: Stiles Eyecare Excellene and Glaucoma Institute, Overland Park, Kansas         
        
        
            Conditions: Glaucoma
        
            
        
    
                
                                    S1827 (MAVERICK) Testing Whether the Use of Brain Scans Alone Instead of Brain Scans Plus Preventive Brain Radiation Affects Lifespan in Patients With Small Cell Lung Cancer
                                
            
            
        Recruiting
                            
            
                This phase III trial studies magnetic resonance imaging (MRI) surveillance and prophylactic cranial irradiation (PCI) to see how well they work compared to MRI surveillance alone in treating patients with small cell lung cancer. MRI scans are used to monitor the possible spread of the cancer with an MRI machine over time. PCI is radiation therapy that is delivered to the brain in hopes of preventing spread of cancer into the brain. The use of brain MRI alone may reduce side effects of receiving...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/20/2025
            
            Locations: University of Kansas Cancer Center-Overland Park, Overland Park, Kansas         
        
        
            Conditions: Extensive Stage Lung Small Cell Carcinoma, Limited Stage Lung Small Cell Carcinoma, Lung Small Cell Carcinoma
        
            
        
    
                
                                    ZILRETTA in Subjects With Shoulder Osteoarthritis
                                
            
            
        Recruiting
                            
            
                Primary Objective: To assess the efficacy of ZILRETTA on pain following an intra-articular (IA) injection in subjects with glenohumeral osteoarthritis (OA) relative to normal saline placebo
Secondary Objective:
* To assess the efficacy of ZILRETTA on pain following an IA injection in subjects with glenohumeral OA relative to triamcinolone acetonide injectable suspension, immediate release (TCA-IR) and normal saline placebo
* To assess the safety of ZILRETTA in subjects with glenohumeral OA rel...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 50 years and 80 years
            Trial Updated:
                05/19/2025
            
            Locations: Kansas City Bone & Joint Clinic - Overland Park, Overland Park, Kansas         
        
        
            Conditions: Glenohumeral Osteoarthritis
        
            
        
    
                
                                    A Study to Compare Two Surgical Procedures in Individuals With BRCA1 Mutations to Assess Reduced Risk of Ovarian Cancer
                                
            
            
        Recruiting
                            
            
                This clinical trial evaluates how well two surgical procedures (bilateral salpingectomy and bilateral salpingo-oophorectomy) work in reducing the risk of ovarian cancer for individuals with BRCA1 mutations. Bilateral salpingectomy involves the surgical removal of fallopian tubes, and bilateral salpingo-oophorectomy involves the surgical removal of both the fallopian tubes and ovaries. This study may help doctors determine if the two surgical procedures are nearly the same for ovarian cancer risk...  Read More             
        
        
    Gender:
                FEMALE
            Ages:
                Between 35 years and 50 years
            Trial Updated:
                05/15/2025
            
            Locations: University of Kansas Hospital-Indian Creek Campus, Overland Park, Kansas         
        
        
            Conditions: Ovarian Carcinoma
        
            
        
    
                
                                    Study of Sacituzumab Govitecan-hziy Versus Treatment of Physician's Choice in Patients With Previously Untreated Locally Advanced Inoperable or Metastatic Triple-Negative Breast Cancer
                                
            
            
        Recruiting
                            
            
                The primary objective of this study is to compare the progression-free survival (PFS) between sacituzumab govitecan-hziy (SG) versus treatment of physician's choice (TPC) in participants with previously untreated, locally advanced, inoperable or metastatic triple-negative breast cancer whose tumors do not express programmed cell death ligand 1 (PD-L1) or in participants previously treated with anti-programmed cell death (ligand or protein) 1 (Anti-PD-(L)1) Agents in the early setting whose tumor...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/15/2025
            
            Locations: The University of Kansas Cancer Center,12200 W. 110th Street, Overland Park, Kansas  +2 locations         
        
        
            Conditions: Triple Negative Breast Cancer, PD-L1 Negative
        
            
        
    
                
                                    Study to Assess the Efficacy and Safety of Iovera®° System in Subjects With Upper Extremity Spasticity
                                
            
            
        Recruiting
                            
            
                This multicenter, randomized, double-blind, sham-controlled study is designed to evaluate the efficacy and safety of the iovera° system in subjects with upper extremity spasticity. A total of approximately 132 subjects will be enrolled; 88 subjects will receive treatment with the iovera° system and 44 subjects will receive sham treatment (sham iovera° system treatment).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/14/2025
            
            Locations: Kansas Institute of Research - Kansas City Bone & Joint Clinic, Overland Park, Kansas         
        
        
            Conditions: Spasticity, Cerebral or Spinal Condition
        
            
        
    
                
                                    S1501 Carvedilol in Preventing Cardiac Toxicity in Patients With Metastatic HER-2-Positive Breast Cancer
                                
            
            
        Recruiting
                            
            
                This phase III trial studies how well carvedilol works in preventing cardiac toxicity in patients with human epidermal growth factor receptor (HER)-2-positive breast cancer that has spread to other places in the body. A beta-blocker, such as carvedilol, is used to treat heart failure and high blood pressure, and it may prevent the heart from side effects of chemotherapy.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/12/2025
            
            Locations: Menorah Medical Center, Overland Park, Kansas  +3 locations         
        
        
            Conditions: Cardiotoxicity, HER2/Neu Positive, Metastatic Malignant Neoplasm in the Brain, Recurrent Breast Carcinoma, Stage IV Breast Cancer AJCC v6 and v7
        
            
        
    109 - 120 of 178
            