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Efficiency of unani formulation in ringworm disease

Phase 2
Conditions
Health Condition 1: L088- Other specified local infections of the skin and subcutaneous tissue
Registration Number
CTRI/2022/03/041124
Lead Sponsor
ational Institute of Unani Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

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

ï??Patients aged 18-60 years of either sex with a clinical diagnosis of Tinea corporis and/or Tinea cruris with <= 5% body surface area involvement

ï??Patients with Global assessment score of >= 5 with positive KOH mount

ï??Patients who will give consent and are able to do follow up

Exclusion Criteria

ï??Immuno-compromised patients

ï??Patients with extensive Dermatophytosis, other forms of tinea infections, superadded bacterial infection

ï??Patients with contact dermatitis, atopic dermatitis, psoriasis, other skin diseases

ï??Patients with a history of hypersensitivity to allylamine antifungals

ï??Patients who received topical antifungal within 1 week and systemic antifungals within 4 weeks prior to enrolment

ï??Patients with a known history or clinical evidence of bleeding disorders, severe systemic illness and uncontrolled diabetes mellitus

ï??Pregnant and lactating females

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Comparison of achieved complete clearance among groups at the end of treatmentTimepoint: Baseline and after treatment
Secondary Outcome Measures
NameTimeMethod
a.Comparison of achieved clinical cure among groups at the end of treatment <br/ ><br>b.Comparison of achieved Mycological cure among groups at the end of treatment <br/ ><br>c.Comparison of relapse among groups at the end of treatment <br/ ><br>d.Improvement in DLQI <br/ ><br>Timepoint: before and After study
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