Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID07618884

TransREctus Sheath PrePeritoneal Procedure (TREPP) for Inguinal Hernia Repair: A Single-center Prospective Study

Led by Assiut University · Updated on 2026-06-01

30

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Inguinal hernia repair is one of the most common surgeries worldwide, with tension-free mesh repair being the main treatment. This research evaluates the trans rectus sheath extra-peritoneal procedure (TREPP), a minimally invasive open approach that accesses the preperitoneal space through the rectus sheath. TREPP aims to avoid interfering with the inguinal nerves, which are believed to play a key role in chronic postoperative inguinal pain (CPIP), a common long-term issue after open hernia repair. The study involves patients undergoing the TREPP procedure for inguinal hernia repair. TREPP is performed as a minimally invasive open surgery that uses a medial approach through the rectus sheath to reach the preperitoneal space, avoiding the lateral abdominal wall nerves. This prospective cohort study will monitor patients after surgery to evaluate outcomes such as hernia recurrence and chronic pain. Participants will be followed for about one year to assess the primary outcome of hernia recurrence and the secondary outcome of chronic postoperative inguinal pain three months after surgery. Researchers will monitor patients through clinical follow-up visits and assessments to measure these outcomes. The study aims to better understand the effectiveness and safety of the TREPP technique in reducing long-term pain and hernia recurrence.

CONDITIONS

Brief Title

TransREctus Sheath PrePeritoneal Procedure (TREPP) for Inguinal Hernia Repair

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults with primary unilateral or bilateral inguinal hernia
Not Eligible

You will not qualify if you...

  • Strangulated hernias
  • Severe comorbidities precluding surgery (ASA Class IV,V)

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Surgery and Immediate Post-operative Care

Duration - 1 day

Participants undergo the TREPP surgical procedure to repair inguinal hernia and receive immediate post-operative care.

1 surgery visit (in-person)

Post-operative Follow-up

Duration - Up to 1 year

Participants are monitored for recovery, including assessment of chronic postoperative inguinal pain at 3 months and evaluation of hernia recurrence up to 1 year after surgery.

Approximately 4 to 6 follow-up visits over 1 year

Trial Site Locations

Total: 1 location

1

Faculty of Medicine-Assiut University -Assiut-Egypt

Asyut, Asyut Governorate, Egypt, 71515

Actively Recruiting

Loading map...

Research Team

M

Mohamad Raafat, MD

F

Faculty of Medicine-Assiut University

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

Similar Trials

A Pilot Study of Local Anesthesia for Inguinal Hernia Surger...

Inguinal Hernia

Actively Recruiting

3 locations

Activity Restrictions After Inguinal Hernia Repair

Inguinal Hernia

Actively Recruiting

1 location

Chronic Pelvic Pain Management in Female and Male Adult Pati...

Pelvic Pain Syndrome

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here