Evaluation of dexmedetomidine in reducing postoperative ocular pai

Phase 3

• Conditions: Condition 1: Strabismus. Condition 2: Esotropia. Condition 3: Exotropia.; Unspecified strabismus; Unspecified esotropia; Exotropia; H50.9; H50.00; H50.1

• Registration Number: IRCT20200503047291N1
• Lead Sponsor: Mashhad University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 17 August 2020

Recruitment & Eligibility

• Status: Complete
• Sex: All
• Target Recruitment: 30

Inclusion Criteria

Children over 7 years
No other medical problems
No history of surgery or manipulation of the extraocular muscles
strabismus
candidate for extra ocular muscle surgery

Exclusion Criteria

Patients with drug abuse
presence of liver,heart or renal disease
unable to answer questions of checklist

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
The amount of postoperative pain. Timepoint: In the designated hours, 4 hours, 8 hours, 12 hours, 24 hours, 48 hours of surgery, the patient's pain rate was assessed using VAS (Visual analogue scale). Method of measurement: Visual Analogue Scale.