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Reconstructing the ocular surface with grafts of non-ocular origin from the same individual

Not Applicable
Registration Number
CTRI/2009/091/000906
Lead Sponsor
Dr. Radhika Tandon
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
20
Inclusion Criteria

Patients with bilateral ocular surface disease with bilateral limbal stem cell deficiency with vision < 6/60 with quiescent disease for >1yr without inflammation or trachomatous scarring who are willing to give informed consent and come for regular post-op follow-up. Patients should not be long term tobacco users.

Exclusion Criteria

Simultaneous presence of any other ocular anterior segment disease or any other systemic disease which seriously compromises the general condition / immune response of the individual; pregnant / lactating mothers / patients with vision > 6/60; patients who are unwilling to come for regular post-op follow up or those who refuse to give consent to enroll in the study; patients with known hypersensitivity / allergy to common drugs

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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