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comparative evaluation of oral voriconazole and oral ketoconazole in severe fungal keratitis

Phase 4
Conditions
Health Condition 1: null- severe fungal keratitisHealth Condition 2: H169- Unspecified keratitis
Registration Number
CTRI/2016/07/007103
Lead Sponsor
DR R P Centre AIIMS New Delhi
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Open to Recruitment
Sex
Not specified
Target Recruitment
40
Inclusion Criteria

SEVERE FUNGAL KERATITIS

EVIDENCE OF FUNGI IN SMEAR OR CULTURE

VN <3/60

CONSENT

WILLING TO BE TREATED AS INPATIENT AND RETURN IN 3 DAYS TILL EPITHELIZATIO

Exclusion Criteria

EVIDENCE OF BACTERIA OR ACANTHAMOEBA ON STAIN

EVIDENCE OF HERPETIC KERATITIS

B/L OR PERFORATED ULCER

H/O PREVIOUS OCULAR SX

PREGNANCY

IMMMUNOCOMPROMISED

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
VISUAL ACUITYTimepoint: DAY3,7,14,21,28,3 MNTHS
Secondary Outcome Measures
NameTimeMethod
TEAR FILM CONCENTRATION OF DRUG SENSITIVITY AGENTS <br/ ><br>DRUG SENSITIVITY PATTERNTimepoint: DAY7,14,21
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