Evaluation and comparison of the results of hernioplasty treatment by spinal anesthesia and general anesthesia
Phase 2
Recruiting
- Conditions
- Inguinal hernia.Inguinal hernia
- Registration Number
- IRCT20200217046523N6
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Male
- Target Recruitment
- 110
Inclusion Criteria
Diagnosis of inguinal hernia
Patients between 50-60 years
Patients should not be contraindicated for spinal anesthesia or general anesthesia and laparoscopic surgery.
Obtaining written consent
Exclusion Criteria
Patients who have not sought follow-up treatment for any reason
Patients who for any reason do not want to continue to cooperate in this project
History of cardiovascular disease
History of major abdominal surgery
History of any cancer
Immunodeficiency
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 1 hour, 3 hours and 6 hours after surgery. Method of measurement: Visual Analogue Scale questionnaire.
- Secondary Outcome Measures
Name Time Method