N/A
N=10
Controlled Adverse Environment: A Pilot Study to Evaluate Tear Film Stability and Tear Evaporation
Environmental Exposure
Bottom Line
View on ClinicalTrials.gov: NCT01448356 ↗Enrolled (actual)
10
Serious AEs
0.0%
Results posted
Dec 2012
Primary outcome: Primary: Tear Evaporation Rate — 39.0; 44.8; 30.6; 26.7 Watt/meter^2
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- temperature and humidity (Procedure)
- Age
- Adult, Older Adult · 21+ yrs
- Sex
- All
- Sponsor
- Singapore Eye Research Institute
- Primary completion
- Apr 2012
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Tear Evaporation Rate |
39.0; 44.8; 30.6; 26.7 | — |
| SECONDARY Tear Film Break up Time |
5.9; 4.4; 5.0; 4.6 | — |
Summary
Dry eye and ocular surface disease account for a lot of morbidity and socio-economic burden in Asia and the rest of the world. This is a small pilot study to evaluate tear function under different conditions of humidity and temperature. This data will be useful for designing future trials in ocular surface and dry eye. The data will likely be used to propose a larger national funded project involving clinical trials. This study involves collaboration between engineers, ocular surface clinicians as well as specialists from the defence science organisation. When successfully completed, the project will increase the capability of Singapore Eye Research Institute and Singapore National Eye Centre to support future industry and academic research in the ocular surface.
Eligibility Criteria
Inclusion Criteria
- must have undergone screening examination
Exclusion Criteria
- unable to go to the DSO laboratory or undergo any of the study procedures
Data sourced from ClinicalTrials.gov (NCT01448356). 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.