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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.
            745 - 756 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)
                    
                                    
                
                                    Comparing Combinations of Drugs to Treat Newly Diagnosed Multiple Myeloma (NDMM) When a Stem Cell Transplant is Not a Medically Suitable Treatment
                                
            
            
        Recruiting
                            
            
                This phase III trial compares three-drug induction regimens followed by double-or single-drug maintenance therapy for the treatment of newly diagnosed multiple myeloma in patients who are not receiving a stem cell transplant and are considered frail or intermediate-fit based on age, comorbidities, and functional status. Treatment for multiple myeloma includes initial treatment (induction) which is the first treatment a patient receives for cancer followed by ongoing treatment (maintenance) which...  Read More             
        
        
    Gender:
                ALL
            Ages:
                All
            Trial Updated:
                05/29/2025
            
            Locations: Smilow Cancer Hospital-Derby Care Center, Derby, Connecticut         
        
        
            Conditions: Plasma Cell Myeloma
        
            
        
    
                
                                    SV2A Density Cannabis Use Disorder
                                
            
            
        Recruiting
                            
            
                The main purpose of this study is to determine whether hippocampal synaptic vesicle density estimated by hippocampal \[11C\]APP-311/\[11C\]UCB-J binding in individuals diagnosed with cannabis use disorder (CUDs) improves with at least 4 weeks of confirmed abstinence from cannabis, in comparison to healthy controls (HCs). Furthermore, any change in synaptic vesicle density will be placed in functional context by measuring verbal memory, which is sensitive to hippocampal function, before and after...  Read More             
        
        
    Gender:
                ALL
            Ages:
                Between 18 years and 75 years
            Trial Updated:
                05/29/2025
            
            Locations: Yale University School of Medicine, New Haven, Connecticut         
        
        
            Conditions: Cannabis Use Disorder, Healthy
        
            
        
    
                
                                    Safety and Tolerability of Fb-PMT in Recurrent Glioblastoma
                                
            
            
        Recruiting
                            
            
                Glioblastoma is a highly aggressive and fatal form of primary malignant brain tumor with limited treatment options. fb-PMT affects a large group of cancer cell signaling pathways and thus may be effective in heterogeneous, treatment-resistant tumors such as Glioblastoma. fb-PMT also is actively transported across the blood-brain barrier into the brain. This study is being conducted to determine the dose level for further clinical development of fb-PMT to treat recurrent Glioblastoma.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/29/2025
            
            Locations: Smilow Cancer Hospital, New Haven, Connecticut         
        
        
            Conditions: Glioma, Malignant
        
            
        
    
                
                                    A Study of Dostarlimab vs Placebo After Chemoradiation in Adult Participants With Locally Advanced Unresected Head and Neck Squamous Cell Carcinoma
                                
            
            
        Recruiting
                            
            
                The goal of this study is to assess the safety and effectiveness of Dostarlimab compared to Placebo in adult participants with HNSCC (Head and Neck Squamous Cell Carcinoma)             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/28/2025
            
            Locations: GSK Investigational Site, Farmington, Connecticut         
        
        
            Conditions: Neoplasms, Head and Neck
        
            
        
    
                
                                    Exploration of Synaptotrophic Effects of Psilocybin in Opioid Use Disorder (OUD)
                                
            
            
        Recruiting
                            
            
                This study will examine the synaptotrophic effects of psilocybin among medically healthy, detoxified OUD subjects. Eligible OUD participants will undergo pre- and post- psilocybin administration PET scans with the \[11C\]-UCB-J radiotracer while inpatient.             
        
        
    Gender:
                ALL
            Ages:
                Between 21 years and 55 years
            Trial Updated:
                05/28/2025
            
            Locations: Yale University, New Haven, Connecticut         
        
        
            Conditions: Opioid Use Disorder
        
            
        
    
                
                                    A Platform Study of Novel Immunotherapy Combinations as First-Line Treatment in Participants With PD-L1 Positive Recurrent/Metastatic Squamous Cell Carcinoma of the Head and Neck- GALAXIES H&N-202
                                
            
            
        Recruiting
                            
            
                The primary purpose of the study is to evaluate the antitumor activity and safety of novel immunotherapy combinations compared with dostarlimab in participants with Programmed death ligand 1 (PD-L1) positive Recurrent/Metastatic (R/M) Head and Neck Squamous Cell Carcinoma (HNSCC).             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/28/2025
            
            Locations: GSK Investigational Site, New Haven, Connecticut         
        
        
            Conditions: Neoplasms, Head and Neck
        
            
        
    
                
                                    Evaluating the Unmet Needs of Older Adults to Promote Functional Recovery After a Critical Illness
                                
            
            
        Recruiting
                            
            
                This is a prospective longitudinal study that will evaluate the unmet needs of older adults (65 and older) who return home (either directly or after short-term rehab) after an ICU hospitalization, evaluate the association of these unmet needs with clinically relevant outcomes, and assess barriers and facilitators to addressing these unmet needs. The proposed research will inform the development and evaluation of a subsequent intervention to improve functional outcomes among older ICU survivors,...  Read More             
        
        
    Gender:
                ALL
            Ages:
                65 years and above
            Trial Updated:
                05/28/2025
            
            Locations: Yale New Haven Hospital, New Haven, Connecticut         
        
        
            Conditions: Critical Illness, Illness, Critical
        
            
        
    
                
                                    Clinical Study of Ivonescimab for First-line Treatment of Metastatic NSCLC Patients
                                
            
            
        Recruiting
                            
            
                This is a Phase 3 Randomized, double-blind, Multiregional Study of Ivonescimab Combined with Chemotherapy Versus Pembrolizumab Combined with Chemotherapy for the First-line Treatment of Metastatic Non-small Cell Lung Cancer. The primary endpoint is overall survival and progression free survival assessed by investigator. The key secondary endpoints include response and safety.             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/28/2025
            
            Locations: Clinical Study Site, Hartford, Connecticut         
        
        
            Conditions: Non-Small Cell Lung Cancer
        
            
        
    
                
                                    Incremental Hemodialysis for Veterans in the First Year of Dialysis (IncHVets)
                                
            
            
        Recruiting
                            
            
                In this pragmatic clinical trial, which will dovetail with Veterans' routine outpatient dialysis clinic visits in six VA medical centers, the investigators will study 252 Veterans with kidney disease who need to start dialysis treatment. If a Veteran is eligible for the study by making enough residual urine, he/she will have a 50% chance to be offered the usual three-times-per-week dialysis vs. twice-per-week dialysis that is gradually increased to three-times per- week over one year. The invest...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/28/2025
            
            Locations: VA Connecticut Healthcare System West Haven Campus, West Haven, CT, West Haven, Connecticut         
        
        
            Conditions: Chronic Kidney Disease (CKD) Stage 5, Kidney Dysfunction Requiring Dialysis (KDRD), Dialysis Dependency
        
            
        
    
                
                                    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: Yale University, New Haven, Connecticut         
        
        
            Conditions: Lymphoma, Non-Hodgkin, Hodgkin Disease
        
            
        
    
                
                                    TReatment for ImmUne Mediated PathopHysiology
                                
            
            
        Recruiting
                            
            
                TReatment for ImmUne Mediated PathopHysiology (TRIUMPH) is a multi-center, three arm, randomized, controlled trial of immunosuppressive therapy for children with acute liver failure. The study will determine if suppressing inflammatory responses with either corticosteroids or equine anti-thymocyte globulin therapy improves survival for children with this rare, life-threatening condition.             
        
        
    Gender:
                ALL
            Ages:
                Between 1 year and 18 years
            Trial Updated:
                05/28/2025
            
            Locations: Yale New Haven Children's Hospital, New Haven, Connecticut         
        
        
            Conditions: Acute Liver Failure, Fulminant Hepatic Failure, Hepatic Encephalopathy, Acute Liver Injury, Immune Dysregulation
        
            
        
    
                
                                    Study With ABBV-CLS-484 in Participants With Locally Advanced or Metastatic Tumors
                                
            
            
        Recruiting
                            
            
                The study will assess the safety, PK, PD, and preliminary efficacy of ABBVCLS-484 as monotherapy and in combination with a PD-1 targeting agent or with a or a vascular endothelial growth factor receptor (VEGFR) tyrosine kinase inhibitor (TKI).
The trial aims to establish a safe, tolerable, and efficacious dose of ABBVCLS-484 as monotherapy and in combination. The study will be conducted in three parts. Part 1 Monotherapy Dose Escalation, Part 2 Combination Dose Escalation and Part 3 Dose Expans...  Read More             
        
        
    Gender:
                ALL
            Ages:
                18 years and above
            Trial Updated:
                05/28/2025
            
            Locations: Yale University School of Medicine /ID# 225707, New Haven, Connecticut         
        
        
            Conditions: Advanced Solid Tumor Cancer
        
            
        
    