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Weekly Isotretinoin vs Tetracycline for Moderate Acne - Trial NCT06225570

Access comprehensive clinical trial information for NCT06225570 through Pure Global AI's free database. This Phase 1 trial is sponsored by Medical University of South Carolina and is currently Not yet recruiting. The study focuses on Acne Vulgaris. Target enrollment is 50 participants.

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NCT06225570
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT06225570
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Weekly Isotretinoin vs Tetracycline for Moderate Acne
Randomized Controlled Trial of Weekly Oral Isotretinoin vs. Oral Tetracyclines for the Treatment of Moderate Acne Vulgaris

Study Focus

Acne Vulgaris

Isotretinoin

Interventional

drug

Sponsor & Location

Medical University of South Carolina

Timeline & Enrollment

Phase 1

Feb 01, 2024

Jun 01, 2025

50 participants

Primary Outcome

Efficacy using Comprehensive Acne Severity Scale

Summary

In the effort to find better treatments for Moderate Acne, which often relies on long-term
 antibiotic use, researchers are exploring alternative options. While Isotretinoin, a Vitamin
 A derivative, is highly effective for severe acne, its side effects limit its use for milder
 cases. A recent study from our institution investigated a new approach: weekly Isotretinoin
 dosing. The results were promising, with acne improvement and no major side effects. This
 suggests that weekly Isotretinoin could be a successful alternative for moderate acne in both
 males and females. To validate these findings, investigators propose a randomized controlled
 trial comparing weekly Isotretinoin to daily Doxycycline over four months. This study could
 confirm the safety and effectiveness of weekly Isotretinoin, as well as shed light on patient
 satisfaction, and long-term results compared to standard antibiotics. This research may offer
 a breakthrough in treating moderate acne while addressing concerns about antibiotic overuse.

ICD-10 Classifications

Acne vulgaris
Acne
Acne, unspecified
Acnรฉ excoriรฉe
Other acne

Data Source

ClinicalTrials.gov

NCT06225570

Non-Device Trial