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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.
            733 - 744 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)
                    
                                    
                
                                    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: Hartford Hospital, Hartford, Connecticut         
        
        
            Conditions: Platinum-resistant Ovarian Cancer
        
            
        
    
                
                                    Primary Subtalar Arthrodesis for Calcaneal Fractures
                                
            
            
        Recruiting
                            
            
                Management of severe injuries to the heel (displaced intra-articular calcaneus fractures) continues to be a major challenge for orthopedic surgeons. Previous studies have demonstrated poor outcomes, and results show that patients experience long-term pain and decreased quality of life postoperatively. Poor outcomes are driven by pain, in particular, which is linked to post-traumatic subtalar arthritis.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                06/02/2025
            
            Locations: Yale University School of Medicine, New Haven, Connecticut         
        
        
            Conditions: Calcaneus Fracture
        
            
        
    
                
                                    CONVERGE Post-Approval Study (PAS)
                                
            
            
        Recruiting
                            
            
                The primary objective of CONVERGE PAS is to evaluate clinical outcomes (peri-procedural and long-term) in a cohort of patients treated during commercial use of the EPi-Sense® Guided Coagulation System or EPi-Sense ST™ Coagulation System to treat symptomatic long-standing persistent atrial fibrillation (AF) patients who are refractory or intolerant to at least one Class I and/or III AAD.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                06/02/2025
            
            Locations: Bridgeport Hospital System, Bridgeport, Connecticut         
        
        
            Conditions: Chronic Atrial Fibrillation
        
            
        
    
                
                                    CA-4948-101: Open-Label, Dose Escalation and Expansion Trial of Emavusertib (CA-4948) in Relapsed or Refractory Primary Central Nervous System Lymphoma (R/R PCNSL)
                                
            
            
        Recruiting
                            
            
                This is a multi-center, open-label study to evaluate the safety, pharmacokinetics (PK), and anti-cancer activity of oral administration of emavusertib alone or in combination with ibrutinib in adult participants with relapsed or refractory (R/R) hematologic malignancies.
This trial will be completed in four parts. In Part A1, emavusertib will be evaluated first in a dose escalating monotherapy setting to establish the safety and tolerability (complete). In Part A2, emavusertib will be evaluated...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                06/02/2025
            
            Locations: Smilow Cancer Hospital at Yale-New Haven, New Haven, Connecticut         
        
        
            Conditions: Relapsed Hematologic Malignancy, Refractory Hematologic Malignancy, Relapsed Primary Central Nervous System Lymphoma, Refractory Primary Central Nervous System Lymphoma
        
            
        
    
                
                                    Study of ONO-4685 in Patients With Relapsed or Refractory T Cell Lymphoma
                                
            
            
        Recruiting
                            
            
                This study will investigate the safety, tolerability, pharmacokinetics, and preliminary efficacy of ONO-4685 in patients with relapsed or refractory T cell Lymphoma             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                06/01/2025
            
            Locations: Yale Cancer Center, New Haven, Connecticut         
        
        
            Conditions: Relapsed or Refractory T Cell Lymphoma
        
            
        
    
                
                                    Study of Tirabrutinib (ONO-4059) in Patients With Primary Central Nervous System Lymphoma (PROSPECT Study)
                                
            
            
        Recruiting
                            
            
                This study will evaluate the efficacy, safety, and pharmacokinetics of tirabrutinib monotherapy in patients with relapsed or refractory PCNSL (Part A), and tirabrutinib in combination with one of two different high dose methotrexate based regimens (methotrexate/ temozolomide/rituximab or rituximab/methotrexate/procarbazine/ vincristine) as first line therapy in patients with newly diagnosed, treatment naïve PCNSL (Part B)             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                06/01/2025
            
            Locations: Yale Cancer Center, New Haven, Connecticut         
        
        
            Conditions: Refractory Primary Central Nervous System Lymphoma, Primary CNS Lymphoma
        
            
        
    
                
                                    Prevalence of Antibodies and Cytokines in Participants With Chronic Granulomatous Disease
                                
            
            
        Recruiting
                            
            
                This research study is designed to assess the prevalence of specific antibodies and inflammatory cytokines in adult and pediatric participants with CGD.             
        
        
    Gender:
                ALL
            Ages:
                All
            Trial Updated:
                05/30/2025
            
            Locations: Home-based telemedicine, Hartford, Connecticut         
        
        
            Conditions: Chronic Granulomatous Disease (CGD)
        
            
        
    
                
                                    Open-label Study of BBO-8520 in Adult Subjects With KRASG12C Non-small Cell Lung Cancer
                                
            
            
        Recruiting
                            
            
                A first in human study to evaluate the safety and preliminary antitumor activity of BBO-8520, a KRAS G12C (ON and OFF) inhibitor, as a single agent and in combination with pembrolizumab in subjects with locally advanced and unresectable or metastatic non-small cell lung cancer with a KRAS (Kirsten rat sarcoma) G12C mutation.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/30/2025
            
            Locations: Yale Cancer Center, New Haven, Connecticut         
        
        
            Conditions: Non-small Cell Lung Cancer, Metastatic Non-Small Cell Lung Cancer, NSCLC, KRAS G12C, Metastatic Lung Cancer, Advanced Lung Carcinoma
        
            
        
    
                
                                    An Open-Label ProSpective MultiCENTer Study to Evaluate Safety and Tolerability of Dry Powder Inhaled Treprostinil in PH
                                
            
            
        Recruiting
                            
            
                Study LTI-401 is an open-label, multicenter study which will evaluate the safety and tolerability of LIQ861 in subjects who have WHO Group 1 \& 3 PH.             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 80 years
            Trial Updated:
                05/30/2025
            
            Locations: Hartford Hospital, Hartford, Connecticut         
        
        
            Conditions: Pulmonary Hypertension, Interstitial Lung Disease
        
            
        
    
                
                                    Trial of Exercise and Lifestyle for Women With Ovarian and Endometrial Cancer
                                
            
            
        Recruiting
                            
            
                An anticipated 200 women with newly diagnosed ovarian and endometrial cancer scheduled to receive chemotherapy (adjuvant chemotherapy after surgery or neoadjuvant chemotherapy before surgery) will be recruited from Smilow Cancer Hospital Network at Yale Cancer Center (YCC) and Sylvester Comprehensive Cancer Center (SCCC) at University of Miami.
Participants will be randomized to an exercise and medical nutrition intervention arm with weekly counseling sessions throughout chemotherapy, or a cont...  Read More             
        
        
    Gender:
                FEMALE
            Ages:
                18 years and above
            Trial Updated:
                05/30/2025
            
            Locations: Yale University, New Haven, Connecticut         
        
        
            Conditions: Ovarian Cancer
        
            
        
    
                
                                    TTVR Early Feasibility Study
                                
            
            
        Recruiting
                            
            
                The objective of this early feasibility study is to gain early clinical insight into the performance of the Intrepid transcatheter tricuspid valve replacement (TTVR) system intended for transfemoral access to deliver a self-expanding bioprosthetic valve within the tricuspid valve.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/30/2025
            
            Locations: Hartford Hospital, Hartford, Connecticut         
        
        
            Conditions: Tricuspid Regurgitation
        
            
        
    
                
                                    A Phase 1/2 Study to Investigate CRB-701 in Solid Tumors
                                
            
            
        Recruiting
                            
            
                The goal of this clinical trial is to define a safe and effective dose of CRB-701 for participants with solid tumors that are expressing a protein called nectin-4.
The main questions it aims to answer are:
What is the the safe and effective dose of CRB-701 when used alone? What cancers can be treated effectively with CRB-701?
Participants will be asked to attend clinic and be given a intravenous infusion of CRB-701 on its own. They will have blood tests and other assessments to measure whethe...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/29/2025
            
            Locations: Yale Cancer Center, New Haven, Connecticut         
        
        
            Conditions: Solid Tumor, Adult
        
            
        
    