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Completed

NCT Number: NCT06884826

Evaluation of Desarda Technique in Management of Complicated Inguinal Hernia

This study aims to evaluate the desarda technique in management of complicated inguinal hernia.

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Key information

Conditions

Desarda Complicated Hernia Hernia, Abdominal Hernia, Inguinal Inguinal Hernia Pathological Conditions, Anatomical Pathological Conditions, Signs and Symptoms

Age range

14 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Minia University

Minya, Minya Governorate, 61611, Egypt

About this study

Desarda technique is one of the best surgical methods suitable for emergency hernia surgery repair, but there is still limited consensus. The purpose of this study is to assess the Long-term outcome of the pure tissue Desarda technique for the treatment of emergency inguinal hernias repair (Incarcerated, Irreducible, and Obstructed Patients) regarding Postoperative Complications, Groin Pain, and recurrence rate.

Surgical techniques for emergency inguinal hernia surgery remain an important less documented area. Emergency inguinal hernia can have different presentations. Incarceration is characterized by the irreducibility of contents and strangulation by the compromise of the blood supply of the contents (e.g., bowel, omentum).

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age above 14 years old.
  • Irreducible, incarcerated & obstructed inguinal or inguinoscrotal hernia; unilateral or bilateral

Exclusion criteria

  • Recurrent Hernias.
  • Intra-operative finding of separated thin and/or weak external oblique aponeurosis.

Treatment and study plan

Desarda technique

Procedure

Patients will undergo Desarda technique.

Primary outcomes

  1. Incidence of postoperative complications

    Time frame: 24 hours postoperatively

    Incidence of postoperative complications such as groin pain, hemorrhage, infection, seroma, orchitis, and testicular atrophy will be recorded.

Secondary outcomes

  1. Stop of postoperative analgesic

    Time frame: 6 days postoperatively

    Stop of postoperative analgesic (Within 3 days, 3-6 day, More than 6 days) will be recorded.

  2. Incidence of recurrence

    Time frame: 1 year postoperatively

    Incidence of recurrence will be recorded.

Sponsors and collaborators

Lead sponsor

Minia University

Other

Registry information

Important dates

Study start
2022
Primary completion
2024
Study completion
2025
First posted
Mar 19, 2025
Registry last updated
May 19, 2026

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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