Corneal Sensitivity Cross-linking Keratoconus

Keratoconus Clinical Trial

— CSK  

Official title:

Corneal Sensitivity Changes Following Cross-linking for Progressive Lower Stage Keratoconus

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01743443
• Other study ID #: ARVO - BN - 2013
• Status: Completed
• Phase: Phase 2/Phase 3
• First received: December 1, 2012
• Last updated: December 4, 2012
• Start date: March 2009
• Est. completion date: October 2012

Study information

• Verified date: December 2012
• Source: Instituto de Olhos de Goiania
• Contact: n/a
• Is FDA regulated: No
• Health authority: Brazil: National Health Surveillance Agency
• Study type: Interventional

Clinical Trial Summary

To evaluate corneal sensitivity changes following corneal cross-linking (CXL) in patients with progressive lower stage keratoconus.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 19
• Est. completion date: October 2012
• Est. primary completion date: October 2012
• Accepts healthy volunteers: No
• Gender: Both
• Age group: 18 Years to 26 Years

Eligibility

Inclusion Criteria:

• Be at least 18 years of age

• Provide written consent and sign a HIPAA form

• Willingness and ability to follow all instructions and comply with schedule for follow-up visits

• For females capable of becoming pregnant,agreet o have uurine pregnancy testing performed prior to treatment; must not be lactating, and must agree to use a medically acceptable form of birth control for at least one week prior to the treatment and continue to use the method until 1 month after the last dose of investigational product.

• Having topographic evidence of keratoconus which is graded as lower stage progressive keratoconus

• Presence of central or inferior steepening on the Pentacam map

• Steepest keratometry (Kmax) value greater than or equal to 51.00D

• BSCVA of 80 letters or fewer for keratoconus on ETDRS chart

• Contact lens wearers only: remove contact lenses one week prior to the screening refraction

• Contact lens wearers only: manifest refraction must be stable between two visits that occur at least 7 days apart

Exclusion Criteria:

• Contraindications, sensitivity or known allergy to the use of the test articles(S) or their components

• If female, be pregnant, nursing, or planning a pregnancy or have a positive urine pregnancy test at Visit 2 prior to treatment or during the course of the study

• Eyes classified as either normal,atypical normal,keratoconus suspect or mild keratoconus on the severity grading scheme

• A history of the insertion of INTACS in the eye to be treated

• A history of previous limbal relaxing incision procedure in the eye to be treated

• Corneal pachymetry that is <350 microns at the thinnest point measured by Pentacam in the eye to be treated

• Eyes which are aphakic

• Eyes which are pseudophakic and do not have a UV blocking lens implanted

• Previous ocular condition (other than refractive error) in the eye to be treated that may predispose the eye for future complications.

• A history of delayed epithelial healing in the eye to be treated

• Patients with nystagmus or any other condition that would prevent a steady gaze during the treatment or other diagnostic tests

• Patients with a currnet condition that, in the investigator's opinion,would interfere with or prolong epithelial healing

• Taking Vitamin C (ascorbic acid) supplements within 1 week of the crosslinking treatment

• A history of previous corneal crosslinking treatment in the eye to be treated

• Have used an investigational drug or device within 30 days of the study or be concurrently enrolled in another investigational drug or device study within 30 days of the study

Study Design

Endpoint Classification: Safety Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic

Related Conditions & MeSH terms

• Keratoconus

Intervention

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.

Locations

Country	Name	City	State
Brazil	Instituto de Olhos de Goiania	Goiania	GO

Sponsors (1)

Lead Sponsor	Collaborator
Instituto de Olhos de Goiania

Country where clinical trial is conducted

Brazil, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Corneal sensitivity	To evaluate corneal sensitivity changes following corneal cross-linking (CXL) in patients with progressive lower stage keratoconus.	Central corneal sensitivity was measured preoperatively, after 7 days, and once a month after surgery until recovery of the baseline preoperative level. The avarage was 12 weeks	Yes