Skip to content

Jiajianqufengrunmian powder in the Treatment of Acne Vulgaris with Damp Toxicity and Stasis: A multicenter, large sample, placebo-controlled, randomized, double-blind, controlled trial

Jiajianqufengrunmian powder in the Treatment of Acne Vulgaris with Damp Toxicity and Stasis: A multicenter, large sample, placebo-controlled, randomized, double-blind, controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900020479
Enrollment
Unknown
Registered
2019-01-01
Start date
2019-02-01
Completion date
Unknown
Last updated
2019-01-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

acne vulgaris

Interventions

1:modified Qufeng Runfan Powder
2:placebo

Sponsors

China-Japan Friendship Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
15 Years to 30 Years

Inclusion criteria

Inclusion criteria: (1) The clinical diagnosis conforms to the diagnostic criteria of acne vulgaris, the grade I and II of Pillsbury classification method, and the syndrome differentiation criteria of dampness, toxin and blood stasis syndrome in traditional Chinese medicine; (2) Acne vulgaris patients aged 15-30 years in outpatient clinics; (3) untreated persons for nearly a week; (4) Those who consent to treatment and sign written informed consent.

Exclusion criteria

Exclusion criteria: (1) Pregnancy, trauma and other stress states; (2) those who had taken hormones, antibiotics, retinoic acid and other drugs for external use or oral administration within 2 weeks; those who received phototherapy within 2 weeks; (3) Patients with severe primary diseases, such as circulatory system, respiratory system, digestive system, urinary system, endocrine system and hematopoietic system, uncontrolled by routine medication; (4) Those who are participating in other drug clinical trials or who have participated in other clinical trials within one month; (5) People who have allergies to any kind of traditional Chinese medicine or matrix ingredients in this medicine have been exposed to it all over the body or locally.

Design outcomes

Primary

MeasureTime frame
Acne severity score;

Secondary

MeasureTime frame
visia;Soft Skin tester;DLQI;

Countries

China

Contacts

Public ContactBai Yan-Ping

Beijing University of Chinese Medicine

zhi@tsinghua.edu.cn+86 13910758509

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 28, 2026