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The anti-inflammatory effect of Keigai-rengyo-to extract and acupuncture in male patients with acne vulgaris: A randomized controlled pilot study

A randomized controlled clinical trial of Hyeonggaeyeongyotang extract and acupuncture treatment for acne vulgaris male patients

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
CRIS
Registry ID
KCT0000071
Enrollment
44
Registered
2010-12-29
Start date
2009-07-23
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Drug, Medical Device : 1. Keigai-rengyo-to extract: We purchase Keigai-rengyo-to extract from the Han Kook Sin Yak Pharm. Co. Ltd which equipped Korean good manufacturing practice (KGMP) facility. Thi

Sponsors

KyungHee University Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Male

Inclusion criteria

Inclusion criteria: 1. Participants are between 13 to 35 years old in male 2. They have more than 10 papules and less than 20 nodules on the face ( Korean Acne Grading System grade 2 to 4) 3. They have had acne for more than 3 months (chronic stage).

Exclusion criteria

Exclusion criteria: Participants will be excluded for the following reasons: 1) they have used western treatment such as retinoids, antibodies, chemical peeling, intense pulsed light or laser treatment, or traditional Chinese medical treatment such like herbal medicine or acupuncture within 1 month before entry; 2) on screening via blood test, they do not meet the normal range (hemoglobin=10g/dl, platelet=100000/mm3, AST, ALT=40 IU/L, Bun>30mg/dl and Creatinine>1.2mg/dl); 3) they have papules or nodules mainly located on the chest or back; 4) they have keloid acne, corticosteroid acne, or other infectious skin disease; 5) they have internal disease that required treatment without delay; 6) they are unable to comply with the study guidelines.

Design outcomes

Primary

MeasureTime frame
the percentage change of acne inflammatory lesions between baseline and end of trial

Secondary

MeasureTime frame
the percentage change of acne non-inflammatory lesions between baseline and end of trial;the count of inflammatory lesions;the count of non-inflammatory lesions;Skindex-29 (quality of life in patients with skin disease);VAS (Visual Analogue Scale; score 0 (no symptom) to 100 (sever symptom);IGA(investigator Global Assessment; from score 1 (very good) to 5 (very poor)

Countries

Korea, Republic of

Contacts

Public ContactKyu Seok Kim

Kyung Hee University

omdkskim@gmail.com+82-2-958-9499

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Mar 29, 2026