Evaluation of the preventive effects of Aminophylline Plasil and Paracetamol on the pain intensity after strabismus surgery

Phase 3

• Conditions: strabismus.; Exotropia; H50.1

• Registration Number: IRCT20150106020588N6
• Lead Sponsor: Esfahan University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 October 2019

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 120

Inclusion Criteria

abbsence of taking analgesics, paracetamol, aminophylline or plasil in 24 hours before the surgery
Filled written informed consent

Exclusion Criteria

Any background of allergy to Aminophylline Plasil and Paracetamol
Reporting chronic pain prolonged more than 6 months

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Intensity of pain after strabismus surgery. Timepoint: entering the recovery, 30 , 60 mins and 2 , 4,8,16,24 hours after entering to recovery. Method of measurement: VAS.