Comparison of the effect of acupuncture on post operative pain relife in inguinal herniorrhaphy : A clinical trial
Not Applicable
- Conditions
- Inguinal hernia.Unilateral or unspecified inguinal hernia, without obstruction or gangrene
- Registration Number
- IRCT2017012932283N1
- Lead Sponsor
- Vice chancellor for Research and Technology, Islamic Azad University of Shahrood
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
Patients candidate for inguinal herniorrhaphy
Exclusion criteria: Recurrent hernia; bilateral hernia; opium addiction; history of chronic disease
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative pain. Timepoint: every hours up to 12 hours. Method of measurement: Visual Analog Scale(VAS).
- Secondary Outcome Measures
Name Time Method