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Comparing Efficacy of Azithromycin and Probiotics for Treatment of Acne Vulgaris

Comparing Efficacy of Azithromycin and Probiotics for Treatment of Acne Vulgaris

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05629468
Enrollment
75
Registered
2022-11-29
Start date
2021-10-15
Completion date
2022-08-31
Last updated
2022-12-05

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

Conditions

Acne Vulgaris

Brief summary

the goal of this clinical trial is to measure the efficacy of probiotics for treatment of acne vulgaris, to compare it with azithromycin and to measure the synergistic effect of azithromycin and probiotics for treatment of acne vulgaris

Detailed description

this study aims to answer this research question: in patients of acne vulgaris, is use of probiotics as efficacious as azithromycin in treating acne lesions & improving quality of life? total 75 patients were divided into 3 groups. group A received azithromycin, group B received probiotics and group C received both drugs. a topical cream was also advised to all groups. outcome was measured as reduction in total lesion count and improvement in patients' quality of life via reduction in Dermatology Life Quality Index score.

Interventions

DRUGAzithromycin

antibiotic

probiotics

DRUGBenzoyl Peroxide 4 % Topical Cream

topical cream

Sponsors

Pak Emirates Military Hospital
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
15 Years to 35 Years
Healthy volunteers
No

Inclusion criteria

* Diagnosed Patients of Mild and Moderate acne * Aged between 15 and 35 years

Exclusion criteria

* Severe acne or any systemic inflammatory disease * Other oral treatment for acne * Allergic to any drug being used in the study * Pregnancy * PCOs * Any drug which can interact with azithromycin

Design outcomes

Primary

MeasureTime frameDescription
change or reduction in the Total Lesion Countat start of the study (baseline), 2 weeks (1st follow up visit), 4 weeks (2nd follow up visit), 8 weeks (3rd follow up visit) and 12 weeks (4th follow up visit).number of acne lesions are counted at every follow up to see whether lesions are reduced than the baseline or not

Secondary

MeasureTime frameDescription
change or reduction in the Dermatology Life Quality Index scoreat start of the study (baseline) and 12 weeks (last follow up visit).improvement in patients' quality of life was assessed to see whether the score has been reduced than the baseline score or not. it was assessed by a 10-item self assessment questionnaire i.e Dermatology Life Quality Index. the score ranges between 0 to 30. higher score means worst outcome and the lower score means better outcome.

Countries

Pakistan

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026