Comparison of anti-inflammatory eye drops in cataract surgery

Phase 3

• Conditions: Postoperative pain.; Acute pain; R52.0

• Registration Number: IRCT20130719014056N13
• Lead Sponsor: Arak University of Medical Sciences

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 7 February 2023

Recruitment & Eligibility

• Status: Pending
• Sex: All
• Target Recruitment: 99

Inclusion Criteria

Cataract surgery candidate by Phaco method
Obtaining informed consent for the intervention
Age 35 to 85 years both sexes
ASA class 1 and 2

Exclusion Criteria

Lack of patient permission
Presence of mental disorders
History of chronic use of sedatives
Alcohol and drug use
Having an allergy to the drugs used

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Postoperative pain. Timepoint: Every 5 minutes during surgery and recovery and 1, 2 and 4 hours after surgery. Method of measurement: Visual analogue scale.;Mean arterial pressure. Timepoint: Every 5 minutes until the end of the operation and during recovery. Method of measurement: non invasive blood pressure monitoring.;Heart rate. Timepoint: Every 5 minutes until the end of the operation and during recovery. Method of measurement: Cardiac monitoring.;The amount of sedation. Timepoint: Every 5 minutes during surgery and recovery and 1, 2 and 4 hours after surgery. Method of measurement: Ramsay scale.