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Laparoscopic Inguinal Hernia Repair TEP vs TAPP

Comparison Between Laparoscopic Transabdominal Pre-peritoneal (TAPP) Versus Total Extraperitoneal (TEP) for Inguinal Hernia Repair.

Status
Active, not recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07108972
Enrollment
60
Registered
2025-08-07
Start date
2024-05-01
Completion date
2025-12-01
Last updated
2025-08-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Laparoscopic Inguinal Hernia Repair

Brief summary

This study is dedicated to compare between 2 different techniques is the management of inguinal hernia repair using laparoscopic intervention and how it may affect the patients life style covering both benefits and possible adverse affects for each method

Interventions

PROCEDURETransabdominal pre-peritoneal laparoscopic inguinal hernia repair

laparoscopic inguinal hernia repair surgical technique that it's main principal is placing the mesh pre-peritoneally through transabdominal approach

laparoscopic inguinal hernia repair surgical technique that it's main principal is placing the mesh pre-peritoneally through extraperitoneal approach

Sponsors

Sohag University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

\- All patients with inguinal hernias (direct and indirect ؛pubonocele type/funicular type؛) with age between 15 to 60 years and any sex at the period between May 2024 to May 2025 presented electively to the outpatient clinic of the department of General surgery, Sohag University Hospital

Exclusion criteria

* Patients with age below 15 years and more than 60 years. * Patients with mega hernias or complete indirect inguinal hernia. * Patients with obstructed or strangulated inguinal hernia. * Patients with abdominal malignancy & cirrhosis with end stage liver disease. * Pregnancy or planning to become pregnant. * History of forced hernial reduction.

Design outcomes

Primary

MeasureTime frameDescription
Persisting painpost-operatively up to 8 weeksa specific questionnaire will be used to assess the extent and nature of pain post-operative
Hernia recurrencepost-operatively up to 6 months

Secondary

MeasureTime frame
Duration of operation (min)Baseline
Length of hospital stay (Days)up to 2 weeks
Time to return to usual activities (Days)Post-operatively up to 8 weeks

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026