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Evaluating the safety and efficacy of unani formulation in treating N ?r F ?rsi(Eczema)

A Randomized, Parallel Group, Open Label, Active Controlled Clinical Study to evaluate the Safety and Efficacy of Safuf Mu?affi Kh ?? plus topical Unani Formulation in the Management of N ?r F ?rsi (Eczema) - NIL

Status
Active, not recruiting
Phases
Phase 2Phase 3
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2024/11/077215
Enrollment
60
Registered
2024-11-21
Start date
Unknown
Completion date
Unknown
Last updated
2024-12-09

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

Conditions

Health Condition 1: L309- Dermatitis, unspecified Health Condition 2: L309- Dermatitis, unspecified

Interventions

Intervention1: 1.Safuf-e-Musaffi-e-Khas (oral) 2.Marham (Topical) : 1.Safuf-e-Musaffi-e-Khas Dosage form:powder Dose:5gm OD Mode of administration:oral Composition of Safuf-e-Musaffi-e-Khas: Amla (K

Sponsors

National Research Institute of Unani Medicine for Skin Disorders
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1.Participants of any gender between 18 to 65 years 2.Participants having the following any signs and symptoms of disease likeItching, Erythema, Visible flexural eczema, Excoriation, Hyperpigmentation, Burning sensation,Lichenification, Crusting, Dry skin 3.Chronicity of more than 6 months and less than 2 years

Exclusion criteria

Exclusion criteria: 1.Known cases of significant Pulmonary/Cardiovascular/Hepato-renal Dysfunction, Malignancy, HIV infection, AIDS, etc. 2.Any other clinical condition that in the opinion of the investigator wouldcompromise the patient’s safety or successful participation in the trial. 3.Pregnancy and Lactation 4. Known allergy, sensitivity or intolerance to the study drug or any of its ingredients 5. Participants who are using steroids or other drugs 6.Participants with active alcohol intake and/or drug abuse

Design outcomes

Primary

MeasureTime frame
Reduction in EASI Score from baselineTimepoint: 56 DAYS

Secondary

MeasureTime frame
Improvement in CDSQ Score from baselineTimepoint: 56 DAYS

Countries

India

Contacts

Public ContactDr K Mohammed Nasar

National Research Institute of Unani Medicine for Skin Disorders

drnasar.nriumsd@gmail.com8328446962

Outcome results

None listed

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