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Clinical outcomes of Descemet Stripping Only in treatment for Fuchs Endothelial Corneal Dystrophy in Thai participants

Phase 1
Conditions
18 years and older thai participants who have Fuchs Endothelial corneal Dystrophy with clinical presentation of Photophobia or night blindness with Snellen Best Corrected Visual Acuity lower than 20/40with modified Krachmer grading of corneal dystrophy not more than gr.IV
Fuchs Endothelial Corneal Dystrophy , Fuchs Endothelial Dystrophy , FECD ,FED ,Descemet Stripping Only , DSO
Registration Number
TCTR20221019001
Lead Sponsor
/A
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending (Not yet recruiting)
Sex
All
Target Recruitment
5
Inclusion Criteria

1.18 years and older thai participants
2.Patient who have Fuchs Endothelial corneal Dystrophy with clinical presentation of
2.1 Photophobia or visual problems in dim light .
2.2 Snellen Best Corrected Visual Acuity lower than 20/40
2.3 Modified Krachmer grading of corneal dystrophy not more than gr.IV with peripheral corneal endothelial cells greater than 1,000 cells/mm2 and corneal thickness 580-640 um

Exclusion Criteria

1.No light perception
2.Have chronic disease that effect on wound healing process , or uncontrolled underlying disease eg. uncontrolled Hypertension and Chronic kidney disease.
3.Immunocopromise patient.
4.Not well co-operative patient or patient who's inconvenient to follow-up
5.Patient who have other eye pathology that effects on vision eg. infectious/autoimmune keratitis or significant cataract
6.History of Rho Kinase Inhibitors drug allergy

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
visual outcome at 12 months after intervention visual acuity, Endothelial cell count, Corneal Thickness
Secondary Outcome Measures
NameTimeMethod
complication of DSO surgery 12 months after intervention visual acuity, Endothelial cell count, Corneal Thickness
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