Exploring nasal neurostimulation for managing contact lens discomfort

Not Applicable

Completed

• Conditions: Contact lens discomfort; Eye - Diseases / disorders of the eye

• Registration Number: ACTRN12615000745549
• Lead Sponsor: Associate Professor Jennifer P. Craig

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2015-07-20
• Last Update Posted: 13 January 2020

Recruitment & Eligibility

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

Inclusion Criteria

Contact lens wearers reporting end of day discomfort with regular soft contact lens wear

Exclusion Criteria

Non soft contact lens wearers
Contact lens wearers unwilling to wear a fresh pair of lenses at the start of each week
Evidence or history of ocular trauma, infection or surgery
Use of systemic medication that has altered in previous 3 months
Participation in a clinical trial within 3 months of current trial start date
Use of topical medications other than lubricant use for dry eye discomfort

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Hours of comfortable contact lens wear, as advised by daily text or email to the researchers[Day 5 (Values recorded daily over 5 consecutive days)]

Secondary Outcome Measures

Name	Time	Method
Hours of total contact lens wear each day, as advised by daily text or email to the researchers[Day 5 (Values recorded daily over 5 consecutive days)];Number of rescue tear supplement drops required to be instilled to enable wear, as advised by daily text or email to the researchers[Day 5 (Values recorded daily over 5 consecutive days)]