Study of Laparoscopic Inguinal Hernia Repair

NCT02920307 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 400

Last updated 2016-09-30

No results posted yet for this study

Summary

Although mesh fixation has been associated to an increased incidence of nerve injury and involves increased operative costs, many surgeons feel that fixation is necessary to reduce the risk of hernia recurrence. The aim of this study is to evaluate the outcomes of laparoscopic herniorrhaphies performed with and without mesh fixation at our institution.

Conditions

  • Hernia, Inguinal
  • Inguinal Hernia, Direct
  • Inguinal Hernia, Indirect
  • Hernia, Femoral
  • Recurrence
  • Neuralgia, Atypical
  • Neuralgia, Ilioinguinal
  • Neuralgia, Iliohypogastric Nerve

Interventions

PROCEDURE

TEP without fixation

Standard totally extraperitoneal preperitoneal (TEP) inguinal hernia repair

PROCEDURE

TEP with fixation

Standard totally extraperitoneal preperitoneal (TEP) inguinal hernia repair

PROCEDURE

TAPP without fixation

Standard transabdominal preperitoneal (TAPP) inguinal hernia repair without mesh fixation

PROCEDURE

TAPP with fixation

Standard transabdominal preperitoneal (TAPP) inguinal hernia repair

Sponsors & Collaborators

  • Muğla Sıtkı Koçman University

    collaborator OTHER
  • Bahçeşehir University

    collaborator OTHER
  • Medical Park Gaziantep Hospital

    lead OTHER

Principal Investigators

  • Mehmet Kaplan, M.D. · Bahçeşehir Üniversitesi Tıp Fakültesi

  • Onder Ozcan, M.D. · Mugla University, School of Medicine

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-05-31
Primary Completion
2014-09-30
Completion
2016-09-30

Countries

  • Turkey (Türkiye)

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02920307 on ClinicalTrials.gov