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Clinical study of Xiao Cuo Yu Rong Prescription in treatment of moderate and severe acne

Phase 1
Conditions
Acne
Registration Number
ITMCTR2022000071
Lead Sponsor
Guang'anmen Hospital, Chinese Academy of traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
Male
Target Recruitment
Not specified
Inclusion Criteria

(1) Acne patients aged 18-40 in outpatient service;
(2) Those who sign the informed consent form;
(3) The severity of skin lesions was grade II ~ IV.

Exclusion Criteria

(1) Infection, pregnancy, childbirth, trauma and other stress states;
(2) Those who have used retinoids and other external drugs or laser therapy within 2 weeks; Those who have received oral therapy within 4 weeks;
(3) Patients with severe primary, immune and systemic diseases;
(4) Those who are participating in other drug clinical trials or have participated in other clinical trials within one month;
(5) Have ever had systemic or local contact allergy to any traditional Chinese medicine or matrix component in the drug;
(6) The severity of skin lesions is grade I (mild).

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Skin damage points;
Secondary Outcome Measures
NameTimeMethod
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