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Efficacy and safety of 30% supramolecular salicylic acid in the treatment of acne vulgaris in adolescents aged 12-17 years

Efficacy and safety of 30% supramolecular salicylic acid in the treatment of acne vulgaris in adolescents aged 12-17 years

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073469
Enrollment
Unknown
Registered
2023-07-11
Start date
2023-07-15
Completion date
Unknown
Last updated
2023-07-16

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

Conditions

Acne vulgaris in adolescents aged 12-17 years

Interventions

Experimental group:Needle clearing + 30% supramolecular salicylic acid treatment

Sponsors

Chengdu Second People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
12 Years to 17 Years

Inclusion criteria

Inclusion criteria: 1) Male and female, age 12-17 years old; 2) Diagnosed with acne vulgaris, Pillsbury International Improved Classification of facial acne ?-? (see Annex 1); 3) The informed consent must be signed by both the subject and his legal guardian.

Exclusion criteria

Exclusion criteria: 1) have another skin condition that may aggravate the condition, or the investigator believes that this condition may affect the judgment of the test results; 2) Allergic to the test product or hypersensitive physique, female pregnant patients; 3) Patients who took oral antibiotics, glucocorticoids, spironolactones and other anti-androgens and other acne drugs within 4 weeks before the trial; Or patients who have used physical therapy for acne, such as photodynamic, red and blue light treatment; Or patients treated with salicylic acid and hydroxy acid; Or have used other topical acne medications within 2 weeks; 4) Oral retinoic acid within 2 months before the trial (6 months for avitaric acid); 5) Patients with a history of facial injection or surgery 2 months before the trial; 6) Patients with immunodeficiency diseases;(YNMT)·

Design outcomes

Primary

MeasureTime frame
Skin loss rate;GAGS score;

Secondary

MeasureTime frame
Researcher satisfaction;Patient symptom evaluation;Patient efficacy evaluation;Patient satisfaction evaluation;

Countries

China

Contacts

Public ContactWa Qingbiao

Chengdu Second People's Hospital

295615394@qq.com+86 139 8198 7190

Outcome results

None listed

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