A Clinical Study on the Efficacy of Unani Formulations in the Management of Qooba e Ras (Tinea Capitis)

A Single Blind Randomised Clinical Study on the Efficacy of Unani Formulations in the Management of Qooba e Ras (Tinea Capitis) - NIL

Status

Active, not recruiting

Phases

Phase 2

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2026/05/110625

Enrollment

Registered

2026-05-19

Start date

Unknown

Completion date

Unknown

Last updated

2026-06-01

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

Conditions

Health Condition 1: B350- Tinea barbae and tinea capitis

Interventions

Intervention1: Test Drugs - Gandhak (Sulphur), Zaj (Alum) ,Sibr (Aloe barbadensis),Kundur (Boswelia Serrata) ,Samagh e arabi (Acacia senegal) and Sat e Mundi(Sphaeranthus indicus extract).: Topical a

Eligibility

Inclusion criteria

Inclusion criteria: Clinically diagnosed patients of Qooba e Ras Tinea capitis. Patients of either sex. Patients between age group of 5 to 60 years. Willing to comply with the consent.

Exclusion criteria

Exclusion criteria: Children below 5 years of age. Patients above 60 years of age. Patients with comorbid conditions like CKD, DM, HTN. Patients with secondarily infected lesions. Mentally ill patients. Patients who do not want to fill consent form

Design outcomes

Primary

Measure	Time frame
SALT (Severity of Alopecia Tool) Photography of the affected site. Assessment of safety by clinical examination and investigationsTimepoint: 14 th , 28th, 42th , 56 th day	—

Secondary

Measure	Time frame
Reduction of itching, scaling ,erythema,hair loss by clinical examinationTimepoint: 14 th , 28th, 42th , 56 th day	—

Countries

India

Contacts

Public ContactShafeen Ajaz

Ajmal Khan Tibbiya College, Faculty of Unani Medicine,AMU

drzamiramrohi@gmail.com8475007594

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026