Clinical Trials Directory

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

TypeNameDescription
OTHERCochet-Bonnet esthesiometer central corneal sensitivityUsing 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.