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Clinical study of BRODA 2% supramolecular salicylic acid in the treatment of mild to moderate acne vulgaris

Clinical study of BRODA 2% supramolecular salicylic acid in the treatment of mild to moderate acne vulgaris

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200065348
Enrollment
Unknown
Registered
2022-11-02
Start date
2019-08-01
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Mild to moderate acne vulgaris

Interventions

Experimental group:2% supramolecular salicylic acid
The control group:Differin Adapalene gel

Sponsors

The Third Affiliated Hospital of Sun Yat-sen University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years

Inclusion criteria

Inclusion criteria: 1. Male or female aged 18-35 years; 2. Patients with mild to moderate (grade I-II according to the Pillsbury grading system & International improved classification) facial acne vulgaris; 3. 15 < number of acnes + papules + pustules on the subject face (the sum of one or three types of lesions) < 50; 4. Voluntary participation and signing informed consent.

Exclusion criteria

Exclusion criteria: 1. The face has other skin diseases that may affect the judgment of the results ( Except for melasma, freckles and seborrheic dermatitis); 2. People who are allergic to test drugs or have high sensitivity; 3. Pregnancy and lactation; 4. Liver function and/or kidney function laboratory test results are clinically abnormal judged by the doctor; 5. Patients with secondary acne, such as occupational acne and acne caused by corticosteroids; 6. Patients treated with oral antibiotics, glucocorticoids, anti-androgens such as spironolactone and other acne treatment drugs; or treated with physical therapy; or treated with salicylic acid and alpha hydroxy acid within 4 weeks before the trial; 7. Those who took oral tretinoin drugs within 2 months before the trial (6 months before acitretin drugs); 8. Patients with a history of facial injections or surgery 2 months before the trial; 9. Patients with immunodeficiency diseases.

Design outcomes

Primary

MeasureTime frame
acne;pimples;pustules;

Secondary

MeasureTime frame
Trans Epidermal Water Loss;Skin water content;Sebum;Pores;Fine lines;

Countries

China

Contacts

Public ContactLai Wei

The Third Affiliated Hospital of Sun Yat-sen University

pifuke03@163.com+86 13924231198

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026