The city of Hartford, Connecticut, currently has 4 active clinical trials seeking participants for Pain research studies.
MagnetOs Flex Matrix Compared to Trinity Elite Mixed with Local Autograft in Patients Undergoing Up to Four-level Instrumented Posterolateral Fusion
Recruiting
This is a phase IV post-marketing study for MagnetOs Flex Matrix. MagnetOs Flex Matrix is a synthetic bone graft extender product that is routinely used by surgeons as a treatment for patients with degenerative disc disease and undergoing spinal fusion surgery. In this study, MagnetOs Flex Matrix will be used according to the latest U.S. Instructions For Use, specifically as a bone graft extender mixed with autograft in a 1:1 vol.% in the posterolateral spine. Trinity Elite will also be used a... Read More
Gender:
ALL
Ages:
18 years and above
Trial Updated:
01/06/2025
Locations: Hartford Hospital, Hartford, Connecticut
Conditions: Degenerative Disc Disease, Spine Fusion, Leg Pain and/or Back Pain
Effects of Oral Tranexamic Acid Following Total Knee Arthroplasty
Recruiting
The primary purpose of this study is to evaluate postoperative pain. Secondary outcomes evaluated in this study will include range of motion (ROM), opioid consumption, and ambulation. Each outcome measure will be evaluated, oral tranexamic acid (TXA) in the experiment arm and placebo in the control arm, after total knee arthroplasty (TKA) at postoperative days 0-3, and weeks 1, 2, 6, and 12.
Gender:
ALL
Ages:
Between 18 years and 89 years
Trial Updated:
12/09/2024
Locations: Trinity Health Of New England/CT Joint Replacement Institute, Hartford, Connecticut
Conditions: Postoperative Pain
Subpectoral Bupivacaine for Pain Management in Adolescent Reduction Mammaplasty
Recruiting
The main question this randomized control trial aims to answer is: • Is the use of intraoperative subpectoral bupivacaine associated with decreased post-operative pain in adolescent patients who undergo bilateral reduction mammaplasty Participants will be randomized into the study group that intraoperatively receives 20cc of subpectoral bupivacaine injections or into the control group that intraoperatively receives 20cc of injectable saline subpectorally. All participants will keep a pain log... Read More
Gender:
ALL
Ages:
Between 13 years and 25 years
Trial Updated:
09/26/2024
Locations: Connecticut Children's, Hartford, Connecticut
Conditions: Macromastia, Post-operative Pain
Pain and Weight Treatment: Development and Trial of PAW
Recruiting
Pediatric weight management efficacy is impacted by failure to complete treatment protocols and, for those that do complete treatment, a return to unhealthy behaviors. This project tests whether treating pain, a common comorbid condition to pediatric obesity, will enhance treatment. This study will generate results that can be translated into immediate improvements in care for families seeking treatment for pediatric obesity.
Gender:
ALL
Ages:
Between 12 years and 18 years
Trial Updated:
06/12/2024
Locations: Connecticut Children's Medical Center, Hartford, Connecticut
Conditions: Obesity, Adolescent, Pain, Chronic, CBT