Orthokeratology for Keratoconus
Sponsor
Hadassah Medical Organization (Other)
Overall Status
Unknown status
CT.gov ID
NCT00816569
Collaborator
(none)
30
1
1
5.9
5
Study Details
Study Description
Brief Summary
To investigate a possible benefit of Orthokeratology contact lenses to improve uncorrected visual acuity of keratoconus patients
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
|
N/A |
Study Design
Study Type:
Interventional
Anticipated Enrollment
:
30 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Orthokeratology Contact Lenses for Keratoconus
Study Start Date
:
Feb 1, 2009
Anticipated Primary Completion Date
:
Jul 1, 2009
Anticipated Study Completion Date
:
Aug 1, 2009
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Keratoconus One eye of Keratoconus patient |
Device: Orthokeratology contact lenses
Wearing Orthokeratology lens in one eye of a keratoconus patient
|
Outcome Measures
Primary Outcome Measures
- Uncorrected Visual acuity [After 1 month]
Secondary Outcome Measures
- Amount of change in corneal video-topography [At one month]
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
to 45 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
-
Moderate Keratoconus
-
No apical scars
Exclusion Criteria:
-
Advanced Keratoconus
-
Apical scaring
-
Contact lens intolerance
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | : Hadassah Medical Organization, | Jerusalem, | Israel | 91120 |
Sponsors and Collaborators
- Hadassah Medical Organization
Investigators
None specified.Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
,
,
ClinicalTrials.gov Identifier:
NCT00816569
Other Study ID Numbers:
- dvleyes-HMO-CTIL
First Posted:
Jan 1, 2009
Last Update Posted:
Jan 1, 2009
Last Verified:
Dec 1, 2008