Comparison of mesh fixation and non-fixation in laparoscopic Transabdominal prepritoneal inguinal hernia repair
Not Applicable
Recruiting
- Conditions
- K40.90Primary inguinal hernia.Unilateral inguinal hernia, without obstruction or gangrene, not specified as recurrent
- Registration Number
- IRCT20210309050650N2
- Lead Sponsor
- Zanjan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 112
Inclusion Criteria
Patients with primary inguinal hernia
Exclusion Criteria
Age under 18 years
Dementia and other psychological disorders
Impossibility of proper follow-up of the patient
Contraindications to general anesthesia
Contraindications Laparoscopic surgery
Bilateral inguinal Hernia
The hernia has recurred
History of previous abdominal surgery and intra-abdominal adhesions
drug abuse
Taking psychiatric drugs
Liver and kidney diseases
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain in patients. Timepoint: Patients' pain will be assessed on days 2, 7 and the third and sixth months after surgery. Method of measurement: Based on Visual Analogue Scale scale, data would be collected.
- Secondary Outcome Measures
Name Time Method