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Primary Inguinal Hernia clinical trials

View clinical trials related to Primary Inguinal Hernia.

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NCT ID: NCT06406959 Recruiting - Clinical trials for Primary Inguinal Hernia

The Effect of Preemptive Regional Anesthesia (TAP-block) on Acute and Chronic Pain After Transabdominal Preperitoneal Inguinal Hernia Repair (TAPP)

ERA-TAPP
Start date: March 1, 2024
Phase: N/A
Study type: Interventional

The study is devoted to the impact of preemptive regional Transversus abdominal plane block on the postoperative acute and chronic pain after elective Transabdominal preperitoneal (TAPP) inguinal hernia repair.

NCT ID: NCT03488342 Recruiting - Clinical trials for Primary Inguinal Hernia

Rives Technique Versus Lichtenstein Repair for Primary Inguinal Hernia

Start date: September 2015
Phase: N/A
Study type: Interventional

Lichtenstein technique, inserting a mesh over the inguinal cord in the neurological plane, is considered the standard of inguinal hernia repair, but it has 4% recurrence and 12% chronic postoperative pain. Rives technique inserts the mesh in the preperitoneal space behind the neurological plane and the muscular plane, thus better fulfilling the principle of hydrostatics.

NCT ID: NCT01984996 Terminated - Clinical trials for Primary Inguinal Hernia

Freedom Inguinal Hernia Repair System Study

Start date: December 2013
Phase: N/A
Study type: Interventional

The primary objective of this study is to evaluate patient quality-of-life (QOL) after inguinal hernia repair. "Carolinas Comfort Scale" (CCS) assessments will be held at regular intervals. The secondary objective of the study is to follow short-term and long-term study-related complications/adverse events.

NCT ID: NCT01596049 Terminated - Clinical trials for Primary Inguinal Hernia

The Efficacy of a Self-fixating Mesh in Unilateral Open Inguinal Hernia Repair

Start date: May 2012
Phase: N/A
Study type: Observational

This study's objective is to assess the efficacy of a Self-fixating mesh in the surgical repair of unilateral inguinal hernia, which is becoming the new standard of care in open surgical repair of inguinal hernia. The study design is interventional, enrolling 300 patients above 18 years of age, admitted for elective repair in the surgical department of Rambam Medical Health Care Campus, an academic medical center. The study will assess several outcomes including post-surgical pain, recurrence, quality of life and post surgical complications (e.g. wound infection, the formation of hematoma or seroma, etc).