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The effect of topical semisolid formulation of metformin on severity and number of skin lesions in acne patients.

The comparison of therapeutic effect on severity and number of skin lesions, between metformin semisolid formulation and placebo, in patients with mild to moderate Acne vulgaris.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT2017013132319N1
Enrollment
20
Registered
2017-05-01
Start date
2017-05-22
Completion date
Unknown
Last updated
2018-02-22

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: The case group, will receive semisolid formulation of metformin, twice a day, for two months and Azithromycin 250mg caplet will be used every other day. Intervention 2: The control gro
Treatment - Drugs
Placebo
The case group, will receive semisolid formulation of metformin, twice a day, for two months and Azithromycin 250mg caplet will be used every other day.
The control group will receive the base of semisolid formulation, the preparation will be administrated topically , two times in a day and for two months and Azithromycin 250mg caplet will be used eve

Sponsors

Shiraz University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Inclusion criteria:Patients with mild to moderate acne, defined as a score of 1 to 30 on the global acne grading system (GAGS) scale, who did not get any treatment before, or were not satisfied with their previous acne therapies, will be participated in the study after giving written informed consent. Exclusion criteria: Patients will be excluded if they are diabetic or have an uncontrolled systemic disease; have received topical anti acne therapy two months before or during the study or any systemic therapy, 30 days before or during the study; were known to be allergic or sensitive to any of the study medications or their components; have a skin disease that might interfere with the diagnosis or evaluation of their skin lesions; pregnant women and lactating ones.

Exclusion criteria

Exclusion criteria:

Design outcomes

Primary

MeasureTime frame
Skin lesions. Timepoint: 0 , 4 , 8 weeks. Method of measurement: Observation.

Secondary

MeasureTime frame
Patients satisfaction. Timepoint: 0,4,8 weeks. Method of measurement: determined by a 10 point scale ranging.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactDr Nasrin Saki

Shahid Faghihi Skin and Dermatology Clinic- Shiraz-Iran

nasrinsa85@yahoo.com+98 71 3235 1090

Outcome results

None listed

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