N/A
N=400
An Observational Study of Dry Eye Prior to Laser-Assisted in Situ Keratomileusis (LASIK) Therapy
Dry Eye Syndromes
Bottom Line
View on ClinicalTrials.gov: NCT01854905 ↗Enrolled (actual)
400
Serious AEs
—
Results posted
Mar 2014
Primary outcome: Primary: Percentage of Patients in Each Category of the Dry Eye Workshop Severity (DEWS) Scale — 65.0; 29.0; 4.2; 1.8 Percentage of Patients
Study Design & Population
- Study type
- Observational
- Phase
- N/A
- Interventions
- No Treatment (Other)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Allergan
- Primary completion
- Sep 2013
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Percentage of Patients in Each Category of the Dry Eye Workshop Severity (DEWS) Scale |
65.0; 29.0; 4.2; 1.8 | — |
Summary
This is an observational, study of dry eye in patients at the consultation visit prior to LASIK surgery. There is no treatment administered or intervention during the study.
Eligibility Criteria
Inclusion Criteria
- Attending an ophthalmology consultation for LASIK
Exclusion Criteria
- None
Data sourced from ClinicalTrials.gov (NCT01854905). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.