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Evaluating the effect of topical phage cocktail for the treatment of acne

Clinical trial of the effect of topical phage cocktail for the treatment of acne vulgaris

Status
Recruiting
Phases
Phase 3
Study type
Interventional
Source
IRCT
Registry ID
IRCT20111224008507N7
Enrollment
100
Registered
2025-02-10
Start date
2025-02-19
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

Acne vulgaris. Acne vulgaris

Interventions

Intervention 1: Intervention group: In the intervention group, 1% clindamycin topical ointment with a phage cocktail gel is applied for 8 weeks. Every morning and evening, patients wash their face wit

Sponsors

Mazandaran University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 25 Years

Inclusion criteria

Inclusion criteria: Age 12 to 25 years Mild to moderate acne vulgaris

Exclusion criteria

Exclusion criteria: Active cancer Immune system defect History of allergy Uncontrolled systemic disease Receiving topical anti-acne treatment 2 months before or during the study Systemic antibiotic treatment during the study Use of oral contraceptive pills (OCP) and spironolactone 30 days before or during the study History of treatment with systemic retinoids Having a skin disease that may interfere with diagnosis or evaluation

Design outcomes

Primary

MeasureTime frame
Reducing the number of skin lesions. Timepoint: First visit before treatment, second, fourth and eighth weeks. Method of measurement: Skin lesion count.;Reducing the number of inflammatory skin lesions. Timepoint: First visit before treatment, second, fourth and eighth weeks. Method of measurement: Skin lesion count.;Reducing the number of total skin lesions. Timepoint: First visit before treatment, second, fourth and eighth weeks. Method of measurement: Skin lesion count.;Reducing the acne severity index. Timepoint: First visit before treatment, second, fourth and eighth weeks. Method of measurement: Acne severity index = papules + (2 × pustules) + (comedones /4).

Secondary

MeasureTime frame
Side effects such as redness, itching, burning, and inflammation. Timepoint: Second, fourth and eighth weeks. Method of measurement: Asking the patient or the patient's mother.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactMohammadsadegh Rezai

Mazandaran University of Medical Sciences

drmsrezaii@yahoo.com+98 11 3334 2334

Outcome results

None listed

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