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Effect of Haridradi tail in Acne and Pigmentation

Clinical Study to assess the Efficacy and Safety of Haridradya Taila in Acne and Acne-induced Post-inflammatory Hyperpigmentation

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2022/01/039493
Enrollment
50
Registered
2022-01-17
Start date
Unknown
Completion date
Unknown
Last updated
2022-10-17

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

Conditions

Health Condition 1: L810- Postinflammatory hyperpigmentation

Interventions

None listed

Sponsors

Ms Ozone Pharmaceuticals Ltd
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients of either sex having mild to moderate facial Acne and mild to moderate acne induced PIH in clinical features. ïâ??· Patients of age between 18 - 45 years. ïâ??· Willing to take part in study and signing consent form

Exclusion criteria

Exclusion criteria: 1. With Present History of Skin Disease e.g. Psoriasis, Dermatitis, Vitiligo etc. related to face. 2. Person suffering from any infective or contagious skin disease 3. Under medication with antibiotics, antifungal and steroid during last one month. 4. Women on Oral contraceptives 5. Patients of known uncontrolled hormonal disease. 6. Any kind of diagnosed hereditary skin disorder. 7. Patient who had undergone any type of skin treatment like laser therapy in last 6 months

Design outcomes

Primary

MeasureTime frame
Primary endpoint ââ?¬â?? Changes from baseline to the end of trial period in ïâ??· Individual lesion count and overall lesion count in Acne ïâ??· Overall grading of Acne in Investigatorââ?¬â?¢s Global Assessment scale for Acne Timepoint: baseline, 4 weeks and 8 weeks

Secondary

MeasureTime frame
Secondary Endpoint ïâ??· ââ?¬â??Changes from baseline to the end of trial period in Acne induced Post inflammatory hyperpigmentation severity scale Safety/Tolerability Endpoints ïâ??· No visible Erythema, oedema, , scaling, dryness, burning, tingling stinging & itching ïâ??· Monitoring of adverse events throughout the course of the studyTimepoint: baseline, 4 weeks and 8 weeks

Countries

India

Contacts

Public ContactSumit Nathani

National Institute of Ayurveda

sumitnathani2@rediff.com7665809886

Outcome results

None listed

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