Impact of fullring and cross-linking in treatment of keratoconus
- Conditions
- keratoconus.other disorders of cornea
- Registration Number
- IRCT2015030813567N9
- Lead Sponsor
- Vice chancellor for research, Tehran University of Medical Science
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 60
The inclusion criteria: Older than 21 year and less than 35 year ; Glasses or hard contact lens intolerance ; mean keratometery less than 53 diopter ; Central corneal thickness more than 400 micron ; maximum myopia and astigmatism 10 diopter ; Best corrected visual acuity more than 4/10
The exclusion criteria: Central corneal scar ;History of any ocular surgery ;pregnancy and lactation ;History of herpetic keratitis ;History of cross-linking ;Patients with connective tissue diseases
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Visual acuity. Timepoint: Before intervention-one week,one month,three month and six month after intervention. Method of measurement: snellen chart.;Refractive error. Timepoint: Before intervention-one week,one month,three month and six month after intervention. Method of measurement: Retinoscopy.;Keratometery. Timepoint: Before intervention-one week,one month,three month and six month after intervention. Method of measurement: Pentacam.;Corneal high order aberration. Timepoint: Before intervention-one week,one month,three month and six month after intervention. Method of measurement: iTrace.;Depth position of the full ring in corneal stroma. Timepoint: Before intervention-one week,one month,three month and six month after intervention. Method of measurement: OCT Casia.;Corneal endothelial cell count. Timepoint: Before intervention-one week,one month,three month and six month after intervention. Method of measurement: Specular microscopy.
- Secondary Outcome Measures
Name Time Method