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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT06141330
Other study ID # Vit-D
Secondary ID
Status Not yet recruiting
Phase N/A
First received
Last updated
Start date December 1, 2023
Est. completion date March 2024

Study information

Verified date November 2023
Source HITEC-Institute of Medical Sciences
Contact Aqsa Naheed, MBBS
Phone 0323-6513804
Email aqsanahid@gmail.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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.


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 58
Est. completion date March 2024
Est. primary completion date March 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 13 Years to 40 Years
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

Dietary Supplement:
D Max Drops
Vitamin D
Drug:
Azithromycin 250 milligram Oral Capsule
Anti Biotic
Adapalene
Retinoid

Locations

Country Name City State
Pakistan Hitec-Ims Islamabad Punjab

Sponsors (1)

Lead Sponsor Collaborator
HITEC-Institute of Medical Sciences

Country where clinical trial is conducted

Pakistan, 

Outcome

Type Measure Description Time frame Safety issue
Primary Efficacious Improvement in Global Acne Grading System Score from baseline to after 2 months of treatment 2 months
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