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A Clinical Study to compare the Efficacy and Safety of Marham-e-DÄd with Terbinafine in the Management of QÅ«bÄ (Ringworm)

Phase 2
Not yet recruiting
Conditions
Tinea corporis,
Registration Number
CTRI/2023/03/051134
Lead Sponsor
National Research Institute of Unani Medicine for Skin Disorders
Brief Summary

-The prevalence rate of *QÅ«bÄ*(Ringworm) has been found to be 20-25% worldwide.

-It is more prevalent in tropical and subtropical countries like India where the heat and humidity is high throughout the year. –

*-QÅ«bÄ* (Ringworm) also has many ill impact on the patient’s quality of life.

-In conventional medicine, some antifungal drugs are used in the treatment of Ringworm, which are becoming resistant to the organism and also have certain adverse effects with antifungal drugs are erythema, itching, dryness, irritation  nausea, hepatotoxity, abdominal pain, headache, rashes, hypokalemia and oligozoospermia etc.

-Hence, there is need to search more effective and safe drugs in management of *QÅ«bÄ* (Ringworm).keeping this in view, a unani formulation *Marham-e- DÄd* has been selected to evaluate its efficacy and safety in the management of *QÅ«bÄ* (ringworm)

Detailed Description

Not available

Recruitment & Eligibility

Status
Not Yet Recruiting
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Circumscribed lesions having any of the following signs and symptoms on body: .Presence of pruritus and burning .Presence of scales_ .Presence of central clearing .Erythematous papules b) Participants with positive mycology (KOH positive).
  • c)| Participants of either sex in age group of 19-60 years.
Exclusion Criteria
  • a) Co-morbid conditions of the participants b) Pregnant or Lactating Women c) Significant Pulmonary/Cardiovascular/Hepato-renal Dysfunction d) Known cases of Immuno-compromised states (HIV/ AIDS, etc.)/Malignancies Participants not willing to attend treatment schedule regularly e) History of hypersensitivity to Itraconazole and Terbinafine.
  • F) Patient having diabetic.
  • g) Participants using the following medications: .
  • Systemic antifungal within 15 days of baseline visit.
  • Systemic corticosteroids within 15 days of baseline visit.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Total Signs and Symptoms Score(TSSS)42 days
Secondary Outcome Measures
NameTimeMethod
1.Conversion to Negative Mycology2.Systemic Safety Assesssment

Trial Locations

Locations (1)

National Research Institute of Unani Medicine for Skin Disorders

🇮🇳

Hyderabad, TELANGANA, India

National Research Institute of Unani Medicine for Skin Disorders
🇮🇳Hyderabad, TELANGANA, India
Anam Farah Sayyed Nisar
Principal investigator
8055669281
anamsyd1996@gmail.com

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