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A study to evaluate the efficacy and safety of 3 study drugs in treatment of patients with with any type of eczematous disorderassociated with underlying tinea / yeast infection

Phase 4
Completed
Conditions
eczematous disorder with underlying tinea/yeast infection
Registration Number
CTRI/2012/09/003000
Lead Sponsor
Abbott Healthcare Pvt Ltd
Brief Summary

This study is done to evaluated the efficacy and safety of a combination of clobetasol, neomycin and miconazole versus combination of  betamethasone, clotrimazole, neomycin versus combination of betamethasone, gentamicin, miconazole in patients with any type of eczematous disorder associated with underlying tinea / yeast infectionxml:namespace prefix = o ns = "urn:schemas-microsoft-com:office:office" /

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
All
Target Recruitment
54
Inclusion Criteria

•Patients aged 18 years and above diagnosed with any type of eczematous disorder associated presenting clinical features of underlying tinea/yeast infection •Patients who agree to adhere to the study design •Patients who give their consent for participation in this study.

Exclusion Criteria

•Pregnant or lactating females •Indications for use of systemic therapy •Patients sensitive to corticosteroids •Patients who have immune deficiency, hepatic or renal impairment •Patients who have been on any therapy within 1 month prior to enrollment in the study •Patients who are using any other concomitant therapy.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
•Improvement in clinical score from baselineBaseline, Day3, Day5 and Day7
Secondary Outcome Measures
NameTimeMethod
•Improvement in scaling and inflammation•Improvement in burning and itching

Trial Locations

Locations (1)

Anand Bhavan Clinic

🇮🇳

Mumbai, MAHARASHTRA, India

Anand Bhavan Clinic
🇮🇳Mumbai, MAHARASHTRA, India
DrHasmukh Shroff
Principal investigator
9820506431
hjshroff@yahoo.com

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