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Safety and Efficacy Study of Artificial Cornea

NCT01018888 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2013-01-08

No results posted yet for this study

Summary

The purpose of this study is to evaluate the stability of artificial cornea manufactured by Aurolab and to assess its visual outcomes.

Conditions

  • Corneal Transplantation

Interventions

DEVICE

Auro KPro (Keratoprosthesis)

Front plate with optical cylinder, a back plate and a titanium ring to hold the complex together

Sponsors & Collaborators

  • Aurolab

    lead OTHER

Principal Investigators

  • Dr. Jeena Mascarenhas, MBBS, MS · Aravind Eye Hospital, Madurai

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Max Age
80 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-08-31
Primary Completion
2014-06-30
Completion
2014-07-31

Countries

  • India

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01018888 on ClinicalTrials.gov