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Study of the treatment of Acne by Unani ointment

A Clinical Study to Evaluate the Efficacy and Safety of Tila-i Muhasa in the Management of Busur Labaniyya (Acne Vulgaris)

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2017/12/010974
Enrollment
60
Registered
2017-12-26
Start date
Unknown
Completion date
Unknown
Last updated
2021-11-24

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

Conditions

Health Condition 1: L700- Acne vulgaris Health Condition 2: null- Busur Labaniyya (Acne Vulgaris)

Interventions

Intervention1: Group (A) Unani Drugs: Tila-i Muhasa (Local): Patients will be advised to apply Tila-i Muhasa (in the form of paste) locally. 5-10 gm according to affected area, once daily for 42 days.

Sponsors

Central Research Institute of Unani Medicine
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: i)Patients of any sex in the age group between 14 and 40 years ii) Clinically stable patients iii) Patients having the following symptoms of Busur Labaniyya: 1. Comedones 2. Papules 3. Pustules 4. Nodules 5. Itching 6. Erythema

Exclusion criteria

Exclusion criteria: 1. Patients aged 40 years 2. Pregnant or Lactating Women 3. Mentally retarded person 4. Patients on corticosteroid or anticonvulsant therapy or taking oral contraceptives 5. Patients suffering from other concomitant diseases like acne rosacea, acne fulminance, acne necrotica, psoriasis, eczema, etc. 6. Significant Pulmonary/Cardiovascular/Hepato-renal dysfunction 7. Patient not willing to attend treatment schedule regularly

Design outcomes

Primary

MeasureTime frame
The response to treatment will be assessed using the following parameters: 1. Global Acne Grading System (GAGS) 2. Photographic Standards for Acne Grading (PSAG) 3. Photographic Standards for Acne Grading (PSAG)Timepoint: at baseline 2wk 4wk and 6wk

Secondary

MeasureTime frame
To compare the improvement in quality of life in patients with Acne Vulgaris assessed by PGA on VAS and IGATimepoint: at baseline 2wk 4wk and 6wk

Countries

India

Contacts

Public ContactDr Mohammad Nawab

Central Research Institute of Unani Medicine, Hyderabad

ccrumhqrsnd58@gmail.com8700027178

Outcome results

None listed

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