Comparison of Inguinal Hernia Repair with Laparoscopic and open Methods

Not Applicable

• Conditions: Inguinal Hernia.; Unilateral inguinal hernia, without obstruction or gangrene, not specified as recurrent; K40.90

• Registration Number: IRCT20200727048228N1
• Lead Sponsor: Shahid Beheshti University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 September 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 84

Inclusion Criteria

Consent of the Patients
Unilateral Non-Incarcerated Primary Inguinal Hernia (Non-Recurrent)

Exclusion Criteria

Patient Dissent
Recurrent Hernia
Bilateral Hernia
Patients with Underlying Diseases (e.g; Asthma, Benign prostatic hyperplasia, Chronic obstructive pulmonary disease)
Heavy Workers

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Severity of Post-op Pain. Timepoint: Just After Surgery, 8h, 24h, 48h and a week after the operation. Method of measurement: Visual Analogue Scale.;Surgical Site Infection. Timepoint: 2 and 7 days after surgery. Method of measurement: Physical Examination.;Seroma. Timepoint: 2 and 7 days after surgery. Method of measurement: Physical Examination.;Hematoma. Timepoint: 2 and 7 days after surgery. Method of measurement: Physical Examination.;Recurrence. Timepoint: 6 months and a year after surgery. Method of measurement: Physical Examination.