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To study whether adding topical steroid eye drops to the standard of care in acanthamoeba keratitis aids in the healing of the conditio

Phase 3
Conditions
Health Condition 1: H188- Other specified disorders of cornea
Registration Number
CTRI/2024/02/062387
Lead Sponsor
ational Institute of Health-National Eye Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

a) Smear culture PCR Confocal positive Acanthamoeba keratitis

b) Acanthamoeba keratitis patients treated with antiamoebic therapy and have corneal episcleral or anterior chamber inflammation at 4 weeks

c) Appropriate written and informed consent

Exclusion Criteria

a) No consent

b) Fungal or Herpetic keratitis

c) Corneal perforation and impending corneal perforation

d) Prior keratoplasty

e) Visual acuity of No light perception in the affected eye

f) Debilitated patient

g) Patients on systemic corticosteroids

h) Corticosteroids allergy

i) Pregnant mothers

j) Steroids responders

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Improved 6 month best corrected visual acuity and hasten the time for acanthamoeba keratitis clinical resolution in the steroid groupTimepoint: 4 years
Secondary Outcome Measures
NameTimeMethod
To study the contribution of organism virulence factors and host factors for severe inflammatory outcomes by metagenomic deep sequencingTimepoint: 4 years
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