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Desarda Tissue Technique vs Lichtenstein Technique for Primary Inguinal Hernia Repair (HP-tis)

C

Consorci Sanitari de l'Alt Penedès i Garraf

Status

Enrolling

Conditions

Complications of Surgical Procedures or Medical Care
Inguinal Hernia Unilateral

Treatments

Procedure: Lichtenstein
Procedure: Desarda

Study type

Interventional

Funder types

Other

Identifiers

NCT06650878
CSAPG-65

Details and patient eligibility

About

This study aims to evaluate whether a surgical technique (Desarda) is superior to the commonly used surgical technique (Lichtenstein) in inguinal hernia repair concerning the occurrence of postoperative complications. The Lichtenstein technique involves the use of a mesh, while the Desarda technique does not.

Enrollment

478 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Diagnosed with primary inguinal hernia.
  • Body mass index below 31
  • Indication for inguinal hernia repair via anterior approach, either as outpatient surgery (CMA) or elective admission.
  • Legal capacity to provide informed consent.

Exclusion criteria

  • Patients with a weak, thin, or divided external oblique aponeurosis.

  • Participants diagnosed with any of the following conditions:

    • Ongoing oncological disease
    • Cirrhotic patients classified as Child B or higher
  • Women who have previously undergone a cesarean section

  • Cognitive or affective conditions that limit the ability to cooperate with the study procedures

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Triple Blind

478 participants in 2 patient groups

Desarda Technique
Experimental group
Description:
Patients asigned to this arm will be treated with Desarda Technique
Treatment:
Procedure: Desarda
Lichtenstein Technique
Active Comparator group
Description:
Patients asigned to this arm will be treated with Lichtenstein Technique
Treatment:
Procedure: Lichtenstein

Trial contacts and locations

1

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Central trial contact

Javier Errando, MD; Noemi Casaponsa

Data sourced from clinicaltrials.gov

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