Efficacy Assessment of Two Methods for Pain Management Following Anorectal Surgery
Phase 2
- Conditions
- Anorectal Disease.Disease of anus and rectum, unspecified
- Registration Number
- IRCT2016100515640N4
- Lead Sponsor
- Vice chancellor for research, Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
Inclusion Criteria: Patients with American Society of Anesthesiologists (ASA) Class I or II; candidate for elective anorectal surgery under general anesthesia
Exclusion Criteria
Pregnancy; opium addiction; documented cardiovascular or pulmonary disease; allergy to the drugs using in trial
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pain. Timepoint: 0, 6, 12, 24 hours after surgery. Method of measurement: Numerical Rating Scale (NRS).;Patient Satisfaction. Timepoint: Until 24 hours after surgery. Method of measurement: Numerical Rating Scale (NRS).
- Secondary Outcome Measures
Name Time Method Side effects. Timepoint: Until 24 hours after surgery. Method of measurement: Serial physical exam.