Treatment of QÅ«bÄ- (Dermatophytosis) by Unani medicine - Habbe Kibreet Sagheer
- Conditions
- Infections of the skin and subcutaneous tissue,
- Registration Number
- CTRI/2023/04/051529
- Lead Sponsor
- Central Council for Research in Unani Medicine
- Brief Summary
Participants attending the GOPD of National Research Institute of Unani Medicine for Skin Disorders, Hyderabad will be evaluated for presence of *QÅ«bÄ*. The participants will be assessed for clinical and laboratory parameters. If, they do not meet the exclusion criteria and fulfil the inclusion criteria, they will be enrolled in the present study. They will be informed about the nature and objectives of the study, and details of other study related procedures. Written and signed informed consent form will be obtained from the participants before enrolling them into the study. A detailed clinical history will be recorded and complete physical examination will be carried out to record the various signs and symptoms of *QÅ«bÄ*. Blood samples will be collected for pathological and biochemical investigations. Study drug will be dispensed as per schedule and participants will be instructed to take the medicine as per the protocol. i.e. *Habbe Kibreet Sagheer- one pill of 250 mg to be taken twice daily orally with water for 4 weeks.*
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- All
- Target Recruitment
- 100
- QÅ«bÄ (Dermatophytosis) of < 2 weeks duration 2.
- Patients with KOH positive 3.
- lesions having any of the following symptoms: Presence of pruritus and burning, Presence of scales, Presence of central clearing, Erythematous papules.
- 1.Co-morbid conditions of the participants 2.Pregnant or Lactating Women 3.Significant Pulmonary/Cardiovascular/Hepato-renal Dysfunction 4.Known cases of Immuno-compromised states (HIV/ AIDS, etc.) Malignancies •Participants not willing to attend treatment schedule regularly 5.History of hypersensitivity to clotrimazole 6.Participants using the following medications: 7.Systemic antifungal within 15 days of baseline visit.
- 8.Systemic corticosteroids within 15 days of baseline visit.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess the safety of Unani Pharmacopoeial formulation Habbe-kibreet Sagheer in cases of QÅ«bÄ (Dermatophytosis). 1st week , 4th week
- Secondary Outcome Measures
Name Time Method •To assess the efficacy of Unani Pharmacopoeial formulation Habbe-kibreet Sagheer in cases of QÅ«bÄ (Dermatophytosis). 1st, 2nd, 3rd, 4th week
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, IndiaDR SYED GULNAWAZ AHMEDPrincipal investigator9848716693skgulnawaz@gmail.com