Trials / Completed
CompletedNCT03733899
An Investigation of the Impact of Localized Topical Anesthesia of the Ocular Surface on End-of-day Contact Lens Discomfort
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 22 (actual)
- Sponsor
- Johnson & Johnson Vision Care, Inc. · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
This is a controlled, randomized, subject-masked, 3x3 crossover, non-dispensing, contralateral study. Twenty subjects will be recruited based on their scores (with their habitual lenses) from the Contact Lens Dry Eye Questionnaire-8 and examined on four occasions.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIAGNOSTIC_TEST | Local Anesthesia | Minims Proxymetacaine hydrochloride Eye Drops |
| DIAGNOSTIC_TEST | Placebo | Sodium Chloride Solution |
Timeline
- Start date
- 2018-11-07
- Primary completion
- 2019-02-07
- Completion
- 2019-02-07
- First posted
- 2018-11-07
- Last updated
- 2025-04-25
- Results posted
- 2020-02-06
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT03733899. Inclusion in this directory is not an endorsement.