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                    Orlando, FL Paid Clinical Trials
A listing of 697  clinical trials  in Orlando, FL  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            445 - 456 of 697
        
                There are currently 697 clinical trials in Orlando, Florida looking for participants to engage in research studies. Trials are conducted at various facilities, including AdventHealth Orlando, Orlando Clinical Research Center, GSK Investigational Site and Nemours Children's Hospital. 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
                    
                                    
                
                                    First-in-human Study of CRB-601-01 to Treat Patients With Advanced Solid Tumor.
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to determine the safety, blood concentrations and treatment effect of CRB-601 in combination with immunotherapy in patients who have advanced solid tumors (cancer) and have exhausted other therapeutic options.CRB-601 targets a protein called avb8 integrin which is expressed by some cancers and not others. This study will focus on tumor types which are know to highly or moderately express this protein.
Researchers will evaluate the side effects caused by treatment, l...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/29/2025
            
            Locations: Advent Health Oncology Hematology, Orlando, Florida  +1 locations         
        
        
            Conditions: Solid Tumor
        
            
        
    
                
                                    Role of Body Composition in Large for Gestational Age Infants (LGA) With Oral Feeding Difficulty
                                
            
            
        Recruiting
                            
            
                Large for Gestational Age (LGA) infants have excess fat-mass (FM) proportion secondary to prolonged in utero exposure to an energy-rich environment. Our preliminary data suggest that excess FM proportion can be associated with oral feeding delay and a potentially modifiable therapeutic target to improve oral feeding outcomes. The objective of this study is to determine the impact of a short-term Fat-free mass (FFM)-indexed feeding on the oral intake volumes in LGA infants with oral feeding diffi...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 1 week and 10 weeks
            Trial Updated:
                05/28/2025
            
            Locations: Nemours Children's Hospital, Orlando, Florida         
        
        
            Conditions: Body Composition, Nutrition Disorder, Infant, Feeding; Difficult, Newborn
        
            
        
    
                
                                    A Study to Evaluate the Safety, Tolerability, Drug Levels, and Preliminary Efficacy of Relatlimab Plus Nivolumab in Pediatric and Young Adults With Hodgkin and Non-Hodgkin Lymphoma
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to assess the safety, tolerability, drug levels, and preliminary efficacy of relatlimab plus nivolumab in pediatric and young adult participants with recurrent or refractory classical Hodgkin lymphoma and non-Hodgkin lymphoma.             
        
        
    Gender:
                ALL
            Ages:
                30 years and below
            Trial Updated:
                05/28/2025
            
            Locations: Local Institution - 0017, Orlando, Florida         
        
        
            Conditions: Lymphoma, Non-Hodgkin, Hodgkin Disease
        
            
        
    
                
                                    Regorafenib in Combination With Pembrolizumab or Pembrolizumab for MSI-H Colorectal Cancer
                                
            
            
        Recruiting
                            
            
                This is a trial of Regorafenib in combination with pembrolizumab for patients with MSI-H colorectal cancer consisting of lead-in phase examining preliminary efficacy and safety, followed by a randomized phase to further examine efficacy.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/28/2025
            
            Locations: AdventHealth Orlando, Orlando, Florida         
        
        
            Conditions: MSI-H Colorectal Cancer
        
            
        
    
                
                                    Efficacy/Safety of ALTB-268 in Subjects w/Moderately to Severely Active UC Refractory to Biologics
                                
            
            
        Recruiting
                            
            
                ALTB-268-201 is a Phase 2a, multicenter, single arm, multiple-dose, open-label study evaluating the efficacy and safety of ALTB-268 in subjects with moderately to severely active UC. The study consists of a Screening Phase, an Induction Phase, a Maintenance Phase, and an OLE.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                05/28/2025
            
            Locations: Digestive and Liver Center of Florida, LLC, Orlando, Florida         
        
        
            Conditions: Ulcerative Colitis
        
            
        
    
                
                                    A Study of Vedolizumab With and Without Upadacitinib in Adults With Crohn's Disease
                                
            
            
        Recruiting
                            
            
                The main aim of this study is to learn whether vedolizumab and upadacitinib given together (also called dual targeted therapy or DTT) reduces bowel inflammation and ulcers in the bowel compared to vedolizumab only (also called monotherapy) in adults with moderately or severely active Crohn's Disease (CD) after 12 weeks of treatment. Other aims are to learn how safe and effective DTT is compared to monotherapy for these participants.
All participants will receive DTT (either vedolizumab and upad...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 65 years
            Trial Updated:
                05/28/2025
            
            Locations: Orlando Health Ambulatory Care Center, Orlando, Florida         
        
        
            Conditions: Crohn's Disease
        
            
        
    
                
                                    STAND - Study of the AGN1 LOEP SV Kit Compared to PMMA in Patients With Vertebral Compression Fractures
                                
            
            
        Recruiting
                            
            
                This is a multicenter, single-blinded, randomized controlled clinical trial evaluating the safety and efficacy of the AGN1 LOEP SV Kit for the treatment of painful vertebral compression fragility fractures (VCFs). The objective of this study is to demonstrate non-inferiority of the AGN1 LOEP SV Kit for the treatment of VCFs to standard of care vertebroplasty treatment using bipedicular injection of PMMA bone cement.             
        
        
    Gender:
                ALL
            Ages:
                50 years and above
            Trial Updated:
                05/27/2025
            
            Locations: Orlando Neurosurgery (Conquest Research), Orlando, Florida         
        
        
            Conditions: Vertebral Compression Fracture, Compression Fracture, Vertebral Compression
        
            
        
    
                
                                    Artificial Intelligence in Endoscopic Ultrasound
                                
            
            
        Recruiting
                            
            
                The objective of the study is to determine if this artificial intelligence system is capable of detecting abnormalities in the pancreas that are identified by an endoscopist at endoscopic ultrasound procedures.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 100 years
            Trial Updated:
                05/27/2025
            
            Locations: Orlando Health, Orlando, Florida         
        
        
            
        
    
                
                                    Study of Bemnifosbuvir/Ruzasvir as a Fixed-dose Combination in Subjects With Normal or Severely Impaired Renal or Hepatic Function
                                
            
            
        Recruiting
                            
            
                To Assess the Effect of Severe Hepatic or Renal Impairment on the Pharmacokinetics of Bemnifosbuvir/Ruzasvir After a Single Dose             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                05/27/2025
            
            Locations: Atea Study Site, Orlando, Florida         
        
        
            Conditions: Healthy Volunteer Study, Hepatic Impairment, Renal Impairment
        
            
        
    
                
                                    A Trial of Centanafadine Efficacy and Safety in Adults With Attention-deficit/Hyperactivity Disorder and Comorbid Anxiety
                                
            
            
        Recruiting
                            
            
                Phase 3b, Randomized, Double-blind, 8-week, Placebo-controlled Trial to Evaluate the Efficacy and Safety of Centanafadine Once Daily Extended-release Capsules for the Treatment of Adults with Attention-deficit/Hyperactivity Disorder and Comorbid Anxiety             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 65 years
            Trial Updated:
                05/27/2025
            
            Locations: Clinical Research Site #006 - CNS Healthcare Orlando, Orlando, Florida         
        
        
            Conditions: ADHD, Anxiety, Generalized Anxiety, Social Anxiety Disorder
        
            
        
    
                
                                    Breaking Disparities in Access to Advanced Diabetes Technologies in Children With Type 1 Diabetes
                                
            
            
        Recruiting
                            
            
                50 children/adolescents (ages 6 to \<18yrs) with T1D in suboptimal control (HbA1c≥8.0%) and lower SES (below 200% poverty line) on insulin therapy (either injections or open-loop pumps) will be recruited at Nemours \~ 1/3 each AA, Hispanic/Latino, non-Hispanic whites. All families that qualify and agree to transition to closed-loop technologies will be recruited to allow data to be gathered before and after use of devices. They will go through the process of approval with the assistance of an in...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 6 years and 17 years
            Trial Updated:
                05/26/2025
            
            Locations: Nemours Children's Health, Orlando, Florida         
        
        
            Conditions: Diabetes Mellitus, Type 1, Child, Delivery of Health Care, Equipment and Supplies
        
            
        
    
                
                                    Lysosomal Acid Lipase (LAL) Deficiency Registry
                                
            
            
        Recruiting
                            
            
                This is an observational, multi-center, international disease registry designed to collect longitudinal data and create a knowledge base that will be utilized to improve the care and treatment of patients with LAL Deficiency. Participation in the Registry by both physicians and patients is voluntary.             
        
        
    Gender:
                ALL
            Ages:
                All
            Trial Updated:
                05/23/2025
            
            Locations: Clinical Trial Site, Orlando, Florida         
        
        
            Conditions: Lysosomal Acid Lipase Deficiency, Cholesterol Ester Storage Disease, Wolman Disease, Acid Cholesteryl Ester Hydrolase Deficiency, Type 2, Acid Lipase Deficiency, LIPA Deficiency, LAL-Deficiency
        
            
        
    445 - 456 of 697
            