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OpenTrials
Completed

NCT Number: NCT06050538

Laparscopic Hernioplasty in Recurrent Inguinal Hernia

The purpose of this study was to compare between laparoscopic transabdominal preperitoneal (TAPP) and totally extraperitoneal (TEP) repair of inguinal hernia in recurrent inguinal hernia.

Completed

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Mansoura University Hospitl

Al Mansurah, Egypt

About this study

The primary objective in this study was to compare postoperative pain between the TAPP group and the TEP group. The secondary objective was to compare operative time, intraoperative complications (bleeding, bowel injury, vascular injury), postoperative complications (hematoma, seroma, wound infection), length of hospital stay and recurrence rate with possible risk factors which include gender, age, BMI ,cord lipomas and location of the hernia.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients diagnosed with unilateral or bilateral recurrent inguinal hernias.
  • Patients between 18 and 70 years old
  • Fit for anesthesia.
  • Agree to participate in the study
  • Both genders were included.

Exclusion criteria

  • Unfitness for general anesthesia and operation.
  • Age < 18 years or >70 years.
  • Complicated hernias (acute irreducible, obstruction or strangulation).
  • The presence of mental or psychological disorders.
  • Refusal to participate in the study.

Treatment and study plan

Transabdominal preperitoneal (TAPP) using polyprolene mesh

Procedure

Transabdominal preperitoneal (TAPP) approach for recurrent inguinal hernia using polyprolene mesh

Total extraperitoneal (TEP) hernioplasty using polyprolene mesh

Procedure

Total extraperitoneal (TEP) approach for recurrent inguinal hernia using polyprolene mesh

Primary outcomes

  1. Postoperative pain

    Time frame: 6 months

    by use of visual analog scale (VAS) where (0) refereed to no pain and (10) refereed to the severest pain.

Secondary outcomes

  1. operative time

    Time frame: 6 months

    operative time by minutes was reported to get mean and standard deviation

  2. complications

    Time frame: 6 months

    complications will be described as number and percentages in each group

Sponsors and collaborators

Lead sponsor

Mansoura University

Other

Registry information

Official study title

A Prospective Randomized Pilot Study Comparing Transabdominal Properitoneal (TAPP) Versus Totally Extra Peritoneal (TEP) Laparoscopic Inguinal Hernioplasty in Recurrent Inguinal Hernia

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Sep 22, 2023
Registry last updated
Sep 22, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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