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Clinical Study of Self-gripping Mesh in TAPP Versus Lichtenstein Hernia Repair

J

Jilin University

Status

Completed

Conditions

Inguinal Hernia

Treatments

Procedure: Lichtenstein hernia repair.
Procedure: Laparoscopic transabdominal preperitoneal hernia repair.

Study type

Interventional

Funder types

Other

Identifiers

NCT06240858
(2022) Annual Audit No. (175)

Details and patient eligibility

About

The goal of this prospective study is to compare the clinical efficacy of self-gripping mesh in laparoscopic transabdominal preperitoneal versus Lichtenstein hernia repair, in order to improve the outcome of inguinal hernia treatment. The main question it aims to answer is, in which procedure is the self-gripping mesh more effective.

Participants will be divided into the TAPP group and the Lichtenstein group by random number table method, the TAPP group underwent laparoscopic transperitoneal preperitoneal hernia repair, and the Lichtenstein group underwent Lichtenstein hernia repair, both groups used self-gripping meshes.

Researchers will compare the operation time, postoperative time out of bed, postoperative hospital stay, hospital costs and postoperative complications between the two groups to see the clinical efficacy of self-gripping mesh in laparoscopic transabdominal preperitoneal versus Lichtenstein hernia repair.

Enrollment

130 patients

Sex

Male

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Male patients aged 18 years and older.
  • Patients with a definite diagnosis of unilateral primary inguinal hernia.
  • Patients and their families were informed about the study protocol and agreed to participate in the study.

Exclusion criteria

  • Patients with femoral, recurrent, bilateral, incarcerated and strangulated hernias.
  • Patients with previous history of lower abdominal surgery.
  • Patients with contraindications to anaesthesia.
  • Patients with contraindications to laparoscopic surgery.
  • Failure to follow up patients as scheduled.
  • Patients with abdominal infections.
  • Those who cannot tolerate general anaesthesia surgery due to serious coagulation disorders, cardiopulmonary disorders, etc.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

130 participants in 2 patient groups

TAPP group
Experimental group
Description:
The TAPP group underwent laparoscopic transperitoneal preperitoneal hernia repair.
Treatment:
Procedure: Laparoscopic transabdominal preperitoneal hernia repair.
Lichtenstein group
Experimental group
Description:
The Lichtenstein group underwent Lichtenstein hernia repair.
Treatment:
Procedure: Lichtenstein hernia repair.

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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