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Hernia Clinical Trials

A listing of Hernia medical research trials actively recruiting patient volunteers. Search for closest city to find more detailed information on a research study in your area.

RESULTS

Found (151) clinical trials

Lotus Clinical Research is conducting a research study to evaluate the efficacy of an investigational pain medication in patients who require hernia repair surgery.

Phase

Lotus Clinical Research is conducting a research study to evaluate the safety and tolerability of an investigational medication in patients following hernia repair surgery.

Phase

Lotus Cinical Research está realizando un studio de investigación que evaluará la seguridad y tolerabilidad de un medicamento experimental en pacientes después de una cirugía de reparación de hernia.

Phase

A Comparison of Fortiva and Strattice Tissue Matrices in Complex Ventral Hernia Repair

This is a randomized, prospective, double-blinded study evaluating the efficacy of Fortiva Porcine Dermis versus Strattice Reconstructive Tissue Matrix in 120 patients with large complex abdominal wall ventral hernias undergoing single stage repair. The patient will be blinded to treatment as well as an independent qualified evaluator to confirm evidence ...

Phase N/A

The neoClose Abdominal Closure vs Carter-Thomason Trial

Both the neoClose abdominal closure to the standard Carter-Thomason closurewill be used to close 12 mm camera and stapler port sites upon completion of a robotic assisted laparoscopic gastric bypass. The procedure requires a 12 mm port be placed in the midline approximately 3 cm cephalad to the umbilicus and ...

Phase N/A

Prospective Analysis of Restorelle in the Treatment of Uterine Prolapse

This study is being done to evaluate the performance of the Restorelle system, which uses Smartmesh - an ultra-lightweight mesh for uterine prolapse management. Most patients undergo a hysterectomy i.e. removal of the uterus when they have a prolapse. However, this has often been found to be an unnecessary operation. ...

Phase N/A

Prevena Incision Management System Wound Care

Compare the outcomes for patients who have abdominal reconstruction for ventral hernia repair, regarding wound morbidity, post-operative pain and patient comfort to ambulation, with the use of Prevena to those patients who have ventral hernia repair to those who have standard wound care.

Phase N/A

A Longitudinal Prospective Outcomes Study of Laparoscopic Abdominal Wall Hernia Repair Using Symbotex Composite Mesh

This study is being done to validate the efficacy of Symbotex™ as an effective synthetic mesh option in the repair of grade I and II ventral hernias. It will also set the groundwork for a future clinical trial in which the efficacy of Symbotex® can be compared to other synthetic ...

Phase

Gastrointestinal Tract Recovery in Patients Undergoing Open Ventral Hernia Repair

Background: One of the most common occurrences following ventral incisional hernia repair is post-operative ileus. Post-operative ileus is a source of patient discomfort and morbidity that ultimately delays discharge from the hospital and is frequently a source of patient readmission. Prolonged length of hospital stay due to post-operative ileus increases ...

Phase N/A

Investigation to Minimize Prolapse Recurrence of the Vagina Using Estrogen

This is a double-blind randomized trial of intravaginal estrogen (conjugated estrogens, 0.625mg/1g cream) vs. placebo in postmenopausal women (n=222 total) with symptomatic prolapse beyond the hymen planning transvaginal native tissue repairs. Medication will be started 6-8 weeks before surgery and continued for 1 year postoperatively, i.e. until scar remodeling is ...

Phase