741624
Last Update Posted: 2009-06-03
Recruiting has ended
All Genders accepted | 18 Years-60 Years |
2 Estimated Participants | No Expanded Access |
Interventional Study | Does not accept healthy volunteers |
Pain Reduce Following Refractive Surgery
applying a material over the exposed stromal bed following refractive surgery to prevent local abrasion and significantly reduce pain
Assessed for pain at 1, 2 and 4 hours and 1, 3 and 5 days. Comparison to non study eye will be performed.
Eligibility
Relevant conditions:
Pain
If you aren't sure if you meet the criteria above speak to your healthcare professional. Criteria may be updated but not reflected here, do not hesitate to contact the study if you think are close to fitting criteria.
locations
Data sourced from ClinicalTrials.gov