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                    Iowa Paid Clinical Trials
A listing of 815  clinical trials  in Iowa  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            541 - 552 of 815
        
                Iowa is currently home to 815 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including Iowa City, Des Moines, Sioux City and West Des Moines. 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)
                    
                                    
                
                                    Investigation to Evaluate the Safety and Effectiveness of Cochlear Implantation in Children and Adults With Unilateral Hearing Loss/Single-sided Deafness
                                
            
            
        Recruiting
                            
            
                The aim of the study is to assess the continued efficacy and safety of cochlear implantation in participants aged 5 years and above with Unilateral Hearing Loss (UHL)/Single Sided Deafness (SSD) supporting a change indication for use.             
        
        
    Gender:
                ALL
            Ages:
                5 years and above
            Trial Updated:
                05/18/2025
            
            Locations: University of Iowa, Iowa City, Iowa         
        
        
            Conditions: Hearing Loss, Unilateral, Deafness, Unilateral
        
            
        
    
                
                                    Evaluation of Genetic Abnormalities Amongst Calcium Phosphate Stone Formers
                                
            
            
        Recruiting
                            
            
                Kidney stones continue to affect more and more people in the United States with the most recent estimate being 1 in 9 people will develop a stone in their life. While family history is a known risk factor for stone disease, it remains unclear whether this is related to learned dietary habits or a truly inheritable genetic condition. Known inheritable genetic conditions linked to stone formation are uncommon, and thus, routine genetic testing is not currently recommended by any major urologic org...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 90 years
            Trial Updated:
                05/16/2025
            
            Locations: University of Iowa, Iowa City, Iowa         
        
        
            Conditions: Nephrolithiasis
        
            
        
    
                
                                    Parkinson's Foundation PD GENEration Genetic Registry
                                
            
            
        Recruiting
                            
            
                Development of a central repository for PD-related genomic data for future research.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/16/2025
            
            Locations: University of Iowa, Iowa City, Iowa         
        
        
            Conditions: Parkinson's Disease
        
            
        
    
                
                                    Testing Olaparib for One or Two Years, With or Without Bevacizumab, to Treat Ovarian Cancer
                                
            
            
        Recruiting
                            
            
                This phase III trial compares the effect of olaparib for one year versus two years, with or without bevacizumab, for the treatment of BRCA 1/2 mutated or homologous recombination deficient stage III or IV ovarian cancer. Olaparib is a polyadenosine 5'-diphosphoribose polymerase (PARP) enzyme inhibitor and may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Bevacizumab is in a class of medications called antiangiogenic agents. It works by stopping the format...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/15/2025
            
            Locations: Mary Greeley Medical Center, Ames, Iowa         
        
        
            Conditions: Fallopian Tube Endometrioid Adenocarcinoma, Fallopian Tube High Grade Serous Adenocarcinoma, FIGO Stage III Ovarian Cancer 2014, FIGO Stage IV Ovarian Cancer 2014, Ovarian Carcinoma, Primary Peritoneal Endometrioid Adenocarcinoma, Primary Peritoneal High Grade Serous Adenocarcinoma, Ovarian High Grade Serous Adenocarcinoma, Ovarian High Grade Endometrioid Adenocarcinoma
        
            
        
    
                
                                    Phase 3 Trial to Evaluate the Efficacy and Safety of Aficamten Compared to Placebo in Adults With Symptomatic nHCM
                                
            
            
        Recruiting
                            
            
                This clinical trial will study the effects of aficamten (versus placebo) on the quality of life, exercise capacity, and clinical outcomes of patients with non-obstructive hypertrophic cardiomyopathy.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 85 years
            Trial Updated:
                05/15/2025
            
            Locations: University of Iowa Hospitals and Clinics, Iowa City, Iowa         
        
        
            Conditions: Symptomatic Non-Obstructive Hypertrophic Cardiomyopathy
        
            
        
    
                
                                    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: University of Iowa Hospitals and Clinics, Iowa City, Iowa         
        
        
            Conditions: Triple Negative Breast Cancer, PD-L1 Negative
        
            
        
    
                
                                    Biorepository and Registry for Plasma Exchange Patients
                                
            
            
        Recruiting
                            
            
                Patients who have immune mediated diseases commonly undergo plasma exchange (PLEX) procedures to remove pathological substances, typically believed to be antibodies. At our facility about 400 of these procedures are performed annually on 40-60 different patients. These procedures are considered within the standard of care for these patients and are covered by insurance. This study will not influence the treatment plan for subjects who participate in this study. The goal of the study is to collec...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 12 years and 99 years
            Trial Updated:
                05/15/2025
            
            Locations: DeGowin blood Center, Iowa City, Iowa         
        
        
            Conditions: Antibody-mediated Rejection, NMO Spectrum Disorder, TTP, CIDP
        
            
        
    
                
                                    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: Heartland Oncology and Hematology LLP, Council Bluffs, Iowa         
        
        
            Conditions: Ovarian Carcinoma
        
            
        
    
                
                                    Evaluation of Dosing Procedures of Chemotherapy Treatment (Carboplatin) With the Contrast Agent Iohexol
                                
            
            
        Recruiting
                            
            
                This trial studies how well iohexol works in helping doctors calculate the dose of carboplatin given to patients with cancer. Drugs used in chemotherapy, such as carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Understanding how to best calculate the dose of carboplatin given to patients with cancer may help doctors learn how to improve the use of carboplatin in the future.             
        
        
    Gender:
                MALE
            Ages:
                18 years and above
            Trial Updated:
                05/15/2025
            
            Locations: UI Health Care Mission Cancer and Blood - Ankeny Clinic, Ankeny, Iowa         
        
        
            Conditions: Malignant Solid Neoplasm
        
            
        
    
                
                                    The Pediatric Anesthesia Quality Improvement Project
                                
            
            
        Recruiting
                            
            
                The Study is designed to collect information about adverse events that occur in children undergoing anesthesia in participating hospitals. Demographic information will be collected on all anesthetics. An analysis of each adverse event will be performed and entered into the database. From this information we will devise strategies to prevent these adverse events.             
        
        
    Gender:
                ALL
            Ages:
                21 years and below
            Trial Updated:
                05/15/2025
            
            Locations: University of Iowa Stead Family Children's Hospital, Iowa City, Iowa         
        
        
            Conditions: Surgery, Anesthesia, Children
        
            
        
    
                
                                    A Phase 2b, Randomized, Double-blind, Active-controlled Study of Single Dose CVXGA Intranasal COVID-19 Vaccine in Adults
                                
            
            
        Recruiting
                            
            
                The purpose of this trial is to assess the safety and relative efficacy of CVXGA (CVXGA50), a KP.2 containing vaccine, compared to COMIRNATY® (COVID-19 Vaccine, mRNA; 2024-2025 Formula), a currently approved COVID-19 vaccine in the prevention of symptomatic, RT-PCR-confirmed SARS-CoV-2 infection. The trial will enroll up to 10016 healthy participants.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 100 years
            Trial Updated:
                05/14/2025
            
            Locations: Velocity Clinical Research, Sioux City, Sioux City, Iowa         
        
        
            Conditions: COVID-19
        
            
        
    
                
                                    A Study to Evaluate Impact of Efanesoctocog Alfa on Long-term Joint Health in Participants With Hemophilia A
                                
            
            
        Recruiting
                            
            
                This is a prospective, observational, multi-center longitudinal cohort study to describe the real-world effectiveness, safety and treatment usage of efanesoctocog alfa in patients with hemophilia A treated per standard of care in the US and Japan.
Patients will be enrolled in the study after the introduction of efanesoctocog alfa in the hemophilia treatment landscape in each study country. Decision to initiate treatment with commercially available efanesoctocog alfa will be made by the treating...  Read More             
        
        
    Gender:
                ALL
            Ages:
                All
            Trial Updated:
                05/13/2025
            
            Locations: University Of Iowa Hospitals And Clinics- Site Number : 8400026, Iowa City, Iowa         
        
        
            Conditions: Hemophilia A
        
            
        
    