Comparison of two analgesic methods in control of Post-operative pai

Not Applicable

• Conditions: Acute pain; Acute post operation pain.

• Registration Number: IRCT201404297829N5
• Lead Sponsor: Vice chancellor for research Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 22 February 2018

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 300

Inclusion Criteria

patients with post operative pain; aged from 15 to 60 years; cooperative psychologically. Exclusion criteria: patients who need another analgesic method; head trauma or unconsciousness; any medical contraindication; aged beneath 15 or above 60 year

Exclusion Criteria

Not provided

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Patients' pain. Timepoint: 30 minutes after the surgery and then 24 hours later. Method of measurement: 0 to 10 visual analogue scale.;Patients' satisfaction. Timepoint: 24 hours after the surgery. Method of measurement: 0 to 100 designed scale.;Addiction. Timepoint: The first day of admission. Method of measurement: Interview.