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Treatment of fungal infection with Unani medicines Qurs Asfar and Zimad e Bars

An Open-Label, Clinical Validation Study to Evaluate the Efficacy and Safety of Unani Pharmacopoeial formulations– Qurs Asfar and Zimad e Bars in Qooba (Dermatophytosis) - Not applicable

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/03/063427
Enrollment
110
Registered
2024-03-01
Start date
Unknown
Completion date
Unknown
Last updated
2024-04-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: B359- Dermatophytosis, unspecified

Interventions

Intervention1: Qurs Asfar and Zimad e Bars: 1Tablet (775mg) twice daily to be taken orally with water and powder as required locally on affected part after rubbing for few seconds twice daily for 6 we

Sponsors

Central Council for Research in Unani Medicine CCRUM New Delhi
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of either sex in the age group of 18-65 years. 2. Subjects confirmed by direct microscopy 3. Clinical signs and symptoms suggestive of fungal infection

Exclusion criteria

Exclusion criteria: 1. Subjects on topical treatment within 2 weeks prior to entry into the study 2. Subjects on systemic therapy within 4 weeks prior to entry into the study 3. Subjects with Tinea capitis (tinea of scalp), Onychomycosis (tinea of nails) and Tinea barbae (tinea of beard) 4. Known cases of allergy to any ingredients of the study drug. 5. Subjects with history of diabetes mellitus and systemic illness requiring long-term treatment. 6. Lactating and pregnant women

Design outcomes

Primary

MeasureTime frame
Improvement in signs and symptoms of Qooba (Dermatophytosis) i.e. Annular/arcuate polycyclic lesion with clear centre, Papulo-vesiculation at margin, Scaling at margin, Erythema, Itching and Burning Timepoint: At baseline, Day 14, 28 and 42.

Secondary

MeasureTime frame
Haematological and biochemical assessment for safety assessment i.e. CBC, LFT, KFT, Urine Routine & microscopic examination.Timepoint: At baseline and end of treatment i.e. day 42

Countries

India

Contacts

Public ContactDr Pradeep Kumar

Central Council for Research in Unani Medicine (CCRUM)

naheedparveen802@gmail.com9213511298

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026