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Clinical Study of the treatment of pimples by Unani ointment.

A Prospective, Randomized, Parallel Group, Open Label, Active Controlled Clinical Study to Evaluate the Efficacy and Safety of a Polyherbal Unani Formulation in the Management of Buthūr Labaniyya (Acne Vulgaris)

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2021/08/036095
Enrollment
60
Registered
2021-08-31
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

Interventions

Intervention1: Polyherbal Unani Formulation (Local): Patients will be advised to apply Unani formulation (in the form of paste) locally on the affected site once daily. Control Intervention1: Benzoyl

Sponsors

National Research Institute of Unani Medicine for Skin Disorders
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients of any sex in the age group between 14 and 40 Years 2. Clinically stable patients 3. Patients having the following symptoms of Buthūr Labaniyya: Comedones, Papules, Pustules, Nodules, Itching, 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 safety to treatment will be assessed by following: 1. Adverse effects 2. Laboratory Investigations (haemogram, LFTs, KFTs).Timepoint: 1. At 2nd wk, 4th wk and 6th wk. 2. At baseline and 6th wk.

Secondary

MeasureTime frame
The response to treatment will be assessed by using the following parameters : 1. Global Acne Grading System (GAGS) 2. Photographic Standards for Acne Grading (PSAG) 3.To compare the improvement in quality of life in patients with Acne Vulgaris assessed by PGA on VAS. 4.Clinical recovery Timepoint: 1. At Fortnightly 2. At baseline and 6th wk. 3. At baseline and 6th wk 4. At Fortnightly

Countries

India

Contacts

Public ContactProf Qamar Uddin

National Research Institute of Unani Medicine for skin disorders

ccrumhqrsnd58@gmail.com8700027178

Outcome results

None listed

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