Clinical Trial of corneal crosslinking for keratoconus and keratoectasia
Not Applicable
- Conditions
- Keratoconus, Keratoectasia
- Registration Number
- JPRN-UMIN000009372
- Lead Sponsor
- the University of Tokyo Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 15
Inclusion Criteria
Not provided
Exclusion Criteria
1)Those undergoing drug therapy for such as glaucoma, more than moderate dry eye or allergy 2)those with ocular disease such as uveitis 3)those with systemic disease that can affect wound healing, such as diabetes 4)Those without obvious progression of the disease for a year before sugery 5)Those with corneal melting disase 6)Those without lens 7)Those with intraocular lens which have no protective function against ultraviolet 8)Woman who are or might be pregnant 9)Lactating woman 10) Those who received other investigational clinical trials within 3 months before the beginning of this study 11) Patients who are judged to be unsuitable as a subject by investigator
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ncorrected and best corrected visual acuity, maximum corneal refractive power in corneal topography
- Secondary Outcome Measures
Name Time Method corneal thickness measured by anterior segment OCT