A randomised cross-over pilot study of Entonox for pain relief in ophthalmic laser

Completed

• Conditions: Signs and Symptoms: Pain; Signs and Symptoms; Pain

• Registration Number: ISRCTN02817810
• Lead Sponsor: Record Provided by the NHSTCT Register - 2004 Update - Department of Health (UK)

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2004-09-30
• Last Update Posted: 13 January 2015

Recruitment & Eligibility

• Status: Completed
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Patients attending for a course of laser pan-retinal photocoagulation will undergo a standardised treatment, receiving entonox on alternative visits. A pain score will be assessed after each treatment.

Exclusion Criteria

Not provided at time of registration

Study & Design

• Study Type: Interventional
• Study Design: Not specified