Inguinal hernia repair with local anesthesia
Not Applicable
- Conditions
- ocal anesthesia.Complication of surgical and medical care, unspecified
- Registration Number
- IRCT201403316803N6
- Lead Sponsor
- Vice chancellor for research, Mazandaran University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Informed written consent; Age between 18 - 70 years; Elective inguinal hernia.
Exclusion criteria: Recurrent hernia; Incarcerated hernia; Hydrocele; Femoral hernia; Bilateral hernia; Pregnancy; Sensitivity to local anesthetic drugs; Diabetes mellitus; Coagulopathy disorder; substance abuse.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Intensity of postoperative pain. Timepoint: At the end of surgery and 3, 6, 12 and 24 hours after surgery. Method of measurement: Visual Analogue Scale.
- Secondary Outcome Measures
Name Time Method Duration of surgery. Timepoint: During surgery. Method of measurement: Questionnaire.;Urinary retention. Timepoint: After surgery. Method of measurement: Questionnaire.;Hematoma in the area of operation. Timepoint: After surgery and at the end of the first week. Method of measurement: Questionnaire.;Surgical site infection. Timepoint: At the end of the first week. Method of measurement: Questionnaire.;Postoperative length of stay. Timepoint: After surgery. Method of measurement: Questionnaire.;Analgesic consumption in the first 24 hours after surgery. Timepoint: In the first 24 hours after surgery. Method of measurement: Questionnaire.