Geneva, Feb. 2 -- International Clinical Trials Registry received information related to the study (ISRCTN13314346) titled 'Intracorneal prosthesis for corneal blindness' on Jan. 23.
Study Type: Interventional
Study Design:
Allocation: N/A: single arm study
Masking: Open (masking not used)
Control: Uncontrolled
Assignment: Single
Purpose: Assessment of the safety of the application of Intra-Ker
Primary Sponsor: Veneto Eye Bank Foundation
Condition:
Corneal blindness
Eye Diseases
Intervention:
Based on the frequency of retroprosthetic inflammatory membranes formation after intraocular prosthesis implant (24.8% in an average follow-up period of 8.5 months), the sample size was estimated that, based on the one-tailed binomial test, ...