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Clinical Trials in China / NCT07007078
Recruiting Phase EARLY_PHASE1

Efficacy of Dihydroartemisinin for Treating Acne Vulgaris

NCT07007078 · tracked via the Priya Life Science China tracker
Sponsor
Shanghai Zhongshan Hospital
Phase
Phase EARLY_PHASE1
Started
2025-06
Last updated
2025-06-05

Condition(s) studied

Acne Vulgaris

Investigational drug(s) / intervention(s)

dihydroartemisinin

dihydroartemisinin: DHA 40mg tid for 90 days

Study summary

The goal of this clinical trial is to learn if dihydroartemisinin (DHA) works to treat Acne Vulgaris in adults. The main question it aims to answer is:

• Does DHA improve the acne severity by at least one grade after treatment. Researchers will treat patients who are clinically diagnosed as Acne Vulgaris to see if DHA works to alleviate the symptoms of Acne Vulgaris.

Participants will:

* Take DHA every day for 3 months
* Visit the clinic once every month for checkups and tests

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
No
Inclusion Criteria: * Clinically diagnosed with acne vulgaris; * For female patients, no pregnancy plans within the next 6 months. Exclusion Criteria: * Patients who have used sex hormones or other systemic medications for acne treatment within the past 3 months; * Patients who have used topical medications for acne within the past 2 weeks; * Pregnant or breastfeeding women; * Patients with known severe diseases of vital organs (e.g., heart, liver, kidney) or malignancies.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Zhongshan Hospital Fudan University Shanghai Shanghai Municipality Recruiting

More Shanghai Zhongshan Hospital trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07007078 on ClinicalTrials.gov ↗ ← All trials in China