Trials / Completed
CompletedNCT00741624
Pain Reduce Following Refractive Surgery
Mitigating Pain Following Refractive Surgery
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 2 (actual)
- Sponsor
- FORSIGHT Vision3 · Industry
- Sex
- All
- Age
- 18 Years – 60 Years
- Healthy volunteers
- Not accepted
Summary
applying a material over the exposed stromal bed following refractive surgery to prevent local abrasion and significantly reduce pain
Detailed description
Assessed for pain at 1, 2 and 4 hours and 1, 3 and 5 days. Comparison to non study eye will be performed.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Bandage | one application for one week |
Timeline
- Start date
- 2008-09-01
- Primary completion
- 2008-10-01
- Completion
- 2008-12-01
- First posted
- 2008-08-26
- Last updated
- 2009-06-03
Locations
1 site across 1 country: Israel
Source: ClinicalTrials.gov record NCT00741624. Inclusion in this directory is not an endorsement.