Trials / Unknown
UnknownNCT02782260
Assessment of the Efficacy of Ocular Dipyridamole in the Treatment of Dry Eye Symptomology in Subjects With Pterygium
- Status
- Unknown
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 40 (estimated)
- Sponsor
- Ariel University · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Subjects with pterygium and associated dry eye symptoms (DES) are randomized into an active cohort (receiving ocular administration of Dipyridamole) or placebo cohort (ocular administration of vehicle). Monthly follow up is conducted for 12 months. Testing conducted at follow up will assess dry eye / pterygium symptoms and endpoints and review the efficacy of the intervention.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | Dipyridamole | |
| DRUG | Placebo |
Timeline
- Start date
- 2016-07-01
- Primary completion
- 2017-10-01
- Completion
- 2018-01-01
- First posted
- 2016-05-25
- Last updated
- 2016-05-25
Source: ClinicalTrials.gov record NCT02782260. Inclusion in this directory is not an endorsement.