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                    Connecticut Paid Clinical Trials
A listing of 1248  clinical trials  in Connecticut  actively recruiting volunteers for paid trials and research studies in various therapeutic areas.
            1237 - 1248 of 1248
        
                Connecticut is currently home to 1248 active clinical trials, seeking participants for engagement in research studies. These trials take place at a variety of cities in the state, including New Haven, Hartford, Farmington and Stamford. 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)
                    
                                    
                
                                    Congenital Heart Disease GEnetic NEtwork Study (CHD GENES)
                                
            
            
        Recruiting
                            
            
                Congenital heart defects (CHD) are the most common major human birth malformation, affecting \~8 per 1,000 live births. CHD are associated with significant morbidity and mortality, and are second only to infectious diseases in contributing to the infant mortality rate. Current understanding of the etiology of pediatric cardiovascular disorders is limited.
The Congenital Heart Disease GEnetic NEtwork Study (CHD GENES) is a multi-center, prospective observational cohort study. Participants will b...  Read More             
        
        
    Gender:
                ALL
            Ages:
                99 years and below
            Trial Updated:
                08/29/2023
            
            Locations: Yale University, New Haven, Connecticut         
        
        
            Conditions: Congenital Heart Defects
        
            
        
    
                
                                    OSTEOAMP Lumbar Fusion Intra-Patient Controlled Study
                                
            
            
        Recruiting
                            
            
                The objective of this clinical study is to compare OSTEOAMP SELECT Fibers to Infuse Bone Graft, in terms of effectiveness and safety, when used as a bone graft substitute in in skeletally mature patients qualified for 2-lumbar interbody fusion (LIF) by means of an intra-patient control model.             
        
        
    Gender:
                ALL
            Ages:
                Between 21 years and 80 years
            Trial Updated:
                08/25/2023
            
            Locations: Yale University, New Haven, Connecticut         
        
        
            Conditions: Lumbar Spine Disease, Lumbar Spondylolisthesis, Lumbar Spine Instability, Lumbar Spondylosis, Degenerative Disc Disease
        
            
        
    
                
                                    Kids Rehydration During Exercise
                                
            
            
        Recruiting
                            
            
                The present study aims to measure the impact of consuming a lower sugar flavored water compared to an equal amount of plain water during exercise on selected rehydration markers in healthy children. Participants will complete two experimental visits designed to examine the differentiating effects of one of two selected beverages (1) lower sugar flavored water beverage and 2) plain water) on certain hydration markers and related perceptual variables during repeated bouts of exercise in a warm env...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 8 years and 10 years
            Trial Updated:
                08/04/2023
            
            Locations: University of Hartford, West Hartford, Connecticut         
        
        
            Conditions: Dehydration in Children, Dehydration Following Exertion (Disorder)
        
            
        
    
                
                                    Assessment of Gait Adaptation Due to an Asymmetric Walking Protocol
                                
            
            
        Recruiting
                            
            
                The purpose of this work is to conduct a comparative research-focused study to evaluate the effectiveness of how purposefully induced asymmetric walking protocols restore healthy, symmetric limb loading in individuals following post-anterior cruciate ligament reconstruction (ACLR) surgery. Additionally, computational modeling and machine learning to model knee loading in the clinic to determine the optimal asymmetric walking protocol to restore healthy gait in post-ACLR individuals.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 30 years
            Trial Updated:
                07/27/2023
            
            Locations: University of Connecticut, Storrs, Connecticut         
        
        
            Conditions: Anterior Cruciate Ligament Reconstruction
        
            
        
    
                
                                    Management of Volume Overload HF Patients by Individual DSR Treatment adJustment-a clinicAl inVestigation of InfusatE2.0
                                
            
            
        Recruiting
                            
            
                This study is a multi-center, prospective, randomized (2:1), open-label study to evaluate the safety and efficacy of DSR therapy using the Infusate 2.0 peritoneal solution (composed of 30% icodextrin and 10% dextrose) in diuretic resistant patients with HF and persistent volume overload.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                07/25/2023
            
            Locations: Yale University, New Haven, Connecticut         
        
        
            Conditions: Heart Failure, Volume Overload
        
            
        
    
                
                                    AMP SCZ® Observational Study: PREDICT-DPACC
                                
            
            
        Recruiting
                            
            
                The Accelerating Medicines Partnership® Schizophrenia (AMP® SCZ) is a large international collaboration to develop algorithms using a set of clinical and cognitive assessments, multi-modal biomarkers, and clinical endpoints that can be used to predict the trajectories and outcomes of individuals at clinical high risk (CHR) for psychosis and to advance the testing of pharmacological interventions for CHR individuals in need. The goal is to accurately predict which individuals are likely to remit,...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 12 years and 30 years
            Trial Updated:
                06/06/2023
            
            Locations: Hartford Healthcare, Hartford, Connecticut         
        
        
            Conditions: Clinical High Risk, Psychosis, Remission, Conversion
        
            
        
    
                
                                    Gedatolisib Plus Fulvestrant With or Without Palbociclib vs Standard-of-Care for the Treatment of Patients With Advanced or Metastatic HR+/HER2- Breast Cancer
                                
            
            
        Recruiting
                            
            
                This is a Phase 3, open-label, randomized, clinical trial evaluating the efficacy and safety of gedatolisib plus fulvestrant with or without palbociclib for the treatment of patients with locally advanced or metastatic HR+/HER2- breast cancer following progression on or after CDK4/6 and aromatase inhibitor therapy.
Condition or disease:
Breast Cancer
Intervention/treatment:
Drug: Gedatolisib
Drug: Palbociclib
Drug: Fulvestrant
Drug: Alpelisib
Phase 3             
        
        
    Gender:
                All
            Ages:
                18 years and above
            Trial Updated:
                08/02/2022
            
            Locations: Yale Cancer Center - New Haven, New Haven, Connecticut         
        
        
            Conditions: Breast Cancer
        
            
        
    
                
                                    Kidney Precision Medicine Project
                                
            
            
        Recruiting
                            
            
                Acute kidney injury (AKI) and chronic kidney disease (CKD) impose a significant global health burden. Yet, no effective therapies currently exist for AKI, and only a few are available for CKD.
Despite significant effort from industry and academia, development of pharmacologic therapies for AKI and CKD has been hampered by:
Non-predictive animal models The inability to identify and prioritize human targets The limited availability of human kidney biopsy tissue A poor understanding of AKI and CK...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/18/2022
            
            Locations: Yale University, New Haven, Connecticut         
        
        
            Conditions: Acute Kidney Failure, Acute Kidney Insufficiency, Acute Renal Failure, Acute Renal Injury, Acute Renal Insufficiency, Kidney Failure, Acute, Kidney Insufficiency, Acute, Renal Failure, Acute, Renal Insufficiency, Acute, Chronic Kidney Diseases, Chronic Kidney Insufficiency, Chronic Renal Diseases, Chronic Renal Insufficiency, Kidney Insufficiency, Chronic
        
            
        
    
                
                                    Introducing Palliative Care (PC) Within the Treatment of End Stage Liver Disease (ESLD)
                                
            
            
        Recruiting
                            
            
                This is a comparative effectiveness study of two pragmatic models aiming to introduce palliative care for end stage liver disease patients. The 2 comparators are:
Model 1: Consultative Palliative Care (i.e. direct access to Palliative Care provider), Model 2: Trained Hepatologist- led PC intervention (i.e. a hepatologist will receive formal training to deliver Palliative Care services)
Primary Outcome: The change in quality of life from baseline to 3 months post enrollment as assessed by FACT-...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 120 years
            Trial Updated:
                04/05/2022
            
            Locations: VA West Haven, West Haven, Connecticut         
        
        
            Conditions: End Stage Liver Disease
        
            
        
    
                
                                    Study of Acalabrutinib (ACP-196) in Combination With Venetoclax (ABT-199), With and Without Obinutuzumab (GA101) Versus Chemoimmunotherapy for Previously Untreated CLL
                                
            
            
        Recruiting
                            
            
                The purpose of this study is to evaluate the efficacy and safety of acalabrutinib in combination with venetoclax and acalabrutinib in combination with venetoclax with and without obinutuzumab compared to chemoimmunotherapy in subjects with previously untreated CLL.             
        
        
    Gender:
                All
            Ages:
                Between 18 years and 130 years
            Trial Updated:
                01/14/2022
            
            Locations: Research Site, Hartford, Connecticut         
        
        
            Conditions: Chronic Lymphocytic Leukemia
        
            
        
    
                
                                    Clinical and Radiographic Outcomes of TLIF w/3D Printed Cellular Implant
                                
            
            
        Recruiting
                            
            
                This study is designed to evaluate clinical outcomes and spine fusion rates for patients undergoing transforaminal lumbar interbody fusion using the CONDUIT 3D printed titanium TLIF cage.             
        
        
    Gender:
                ALL
            Ages:
                Between 35 years and 80 years
            Trial Updated:
                01/14/2022
            
            Locations: Hartford Healthcare Bone and Joint Institute, Hartford, Connecticut         
        
        
            Conditions: Foraminal Stenosis, Degenerative Disc Disease, Lumbar Spondylolisthesis, Lumbar Spinal Stenosis
        
            
        
    
                
                                    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: University of Connecticut Health Center, Farmington, Connecticut         
        
        
            Conditions: Schizophrenia
        
            
        
    