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Vitamin D Supplementation in Acne

H

HITEC-Institute of Medical Sciences

Status

Enrolling

Conditions

Acne Vulgaris

Treatments

Drug: Adapalene
Drug: Azithromycin 250 milligram Oral Capsule
Dietary Supplement: D Max Drops

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The goal of this clinical trial is to compare in acne vulgaris patients. The main question it aims to answer is:

• To assess the therapeutic benefit of vitamin D supplement in acne vulgaris treatment, following a 2-month treatment regimen that includes vitamin D supplementation compared to conventional (systemic azithromycin and topical retinoid) treatment alone.

Participants will receive vitamin D supplements in addition to capsule Azithromycin and topical retinoid.

Researchers will compare groups to determine efficacy of Vitamin D supplements in the treatment of Acne vulgaris.

Enrollment

58 estimated patients

Sex

All

Ages

13 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Individuals aged between 13 and 40 years with diagnoses of Acne vulgaris are included.

Exclusion criteria

  • Individuals currently undergoing treatment for polycystic ovary syndrome (PCOs)
  • Those with obesity
  • Individuals employing vitamin supplementation
  • Those under the influence of topical or systemic steroids and acne treatment in the last 2 months.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

58 participants in 2 patient groups

Vitamin D
Experimental group
Treatment:
Dietary Supplement: D Max Drops
Drug: Azithromycin 250 milligram Oral Capsule
Drug: Adapalene
Placebo
Active Comparator group
Treatment:
Drug: Azithromycin 250 milligram Oral Capsule
Drug: Adapalene

Trial contacts and locations

1

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Central trial contact

Aqsa Naheed, MBBS

Data sourced from clinicaltrials.gov

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