Vitamin D Supplementation in Acne

NCT ID: NCT06141330

Last Updated: 2024-08-29

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

58 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-02-24

Study Completion Date

2024-10-31

Brief Summary

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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.

Detailed Description

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Conditions

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Acne Vulgaris

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Participants

Study Groups

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Vitamin D

Group Type EXPERIMENTAL

D Max Drops

Intervention Type DIETARY_SUPPLEMENT

Vitamin D

Azithromycin 250 milligram Oral Capsule

Intervention Type DRUG

Anti Biotic

Adapalene

Intervention Type DRUG

Retinoid

Placebo

Group Type ACTIVE_COMPARATOR

Azithromycin 250 milligram Oral Capsule

Intervention Type DRUG

Anti Biotic

Adapalene

Intervention Type DRUG

Retinoid

Interventions

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D Max Drops

Vitamin D

Intervention Type DIETARY_SUPPLEMENT

Azithromycin 250 milligram Oral Capsule

Anti Biotic

Intervention Type DRUG

Adapalene

Retinoid

Intervention Type DRUG

Eligibility Criteria

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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.
Minimum Eligible Age

13 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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HITEC-Institute of Medical Sciences

OTHER

Sponsor Role lead

Responsible Party

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Aqsa Naheed

Professor, MBBS, FCPS

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Hitec-Ims

Islamabad, Punjab Province, Pakistan

Site Status RECRUITING

Countries

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Pakistan

Central Contacts

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Aqsa Naheed, MBBS

Role: CONTACT

0323-6513804

Facility Contacts

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Wajeeha Mahjabeen, MBBS

Role: primary

+92 333 4219210

Other Identifiers

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Vit-D

Identifier Type: -

Identifier Source: org_study_id

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