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comparitive study of two antifungal medicines in treatment of superficial fungal infection

Not yet recruiting
Conditions
Fungal infected stable patients.
Registration Number
CTRI/2018/07/015063
Lead Sponsor
IMS BHU
Brief Summary

this is a comparative study with two drugs (terbinafine and itraconazole) with recommended daily doses, double daily doses and combination of both drugs with daily doses. Total study period is of 8 weeks.

primary and secondary outcomes are complete clearing of skin lesions.

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
275
Inclusion Criteria

Tinea cruris Tinea corporis Tinea faciei.

Exclusion Criteria
  • weight more than 80 kg Any other co-morbidities like hepatic disorders, renal disorders, cardiac disorders, etc.
  • history of oral antifungal agents within one month of start of study.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Complete clearance of skin lesionsevery 2 weeks for 8 weeks
Secondary Outcome Measures
NameTimeMethod
Experienced as primary outcome.Every 2 weeks for 8 weeks.

Trial Locations

Locations (1)

Sir Sunderlal Hospital

🇮🇳

Varanasi, UTTAR PRADESH, India

Sir Sunderlal Hospital
🇮🇳Varanasi, UTTAR PRADESH, India
Najuma Subba
Principal investigator
9198120582
najumasubba@gmail.com

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