Trials / Completed
CompletedNCT01743443
Corneal Sensitivity Cross-linking Keratoconus
Corneal Sensitivity Changes Following Cross-linking for Progressive Lower Stage Keratoconus
- Status
- Completed
- Phase
- Phase 2 / Phase 3
- Study type
- Interventional
- Enrollment
- 19 (actual)
- Sponsor
- Instituto de Olhos de Goiania · Academic / Other
- Sex
- All
- Age
- 18 Years – 26 Years
- Healthy volunteers
- Not accepted
Summary
To evaluate corneal sensitivity changes following corneal cross-linking (CXL) in patients with progressive lower stage keratoconus.
Detailed description
Thirty eight eyes of 19 patients (11 women, 8 men) were included in a prospective, nonrandomized clinical study. Mean patient age was 22 years (range, 18-26 years). Inclusion criteria were low stage bilateral progressive keratoconus, transparent cornea and thinnest corneal thickness ≥ 440 µm. Using the Cochet-Bonnet esthesiometer central corneal sensitivity was measured preoperatively, after 7 days, and once a month after surgery until recovery of the baseline preoperative level. Normal levels of central corneal sensitivity were considered above 40mm.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| OTHER | Cochet-Bonnet esthesiometer central corneal sensitivity | Using the Cochet-Bonnet esthesiometer central corneal sensitivity was measured preoperatively, after 7 days, and once a month after surgery until recovery of the baseline preoperative level. Normal levels of central corneal sensitivity were considered above 40mm. |
Timeline
- Start date
- 2009-03-01
- Primary completion
- 2012-10-01
- Completion
- 2012-10-01
- First posted
- 2012-12-06
- Last updated
- 2012-12-06
Locations
1 site across 1 country: Brazil
Source: ClinicalTrials.gov record NCT01743443. Inclusion in this directory is not an endorsement.