The effect of intense pulsed light combined with supramolecular salicylic acid on post-adolescene acne

Status

Recruiting

Phases

Early Phase 1

Study type

Interventional

Source

ChiCTR

Registry ID

ChiCTR1900024848

Enrollment

Unknown

Registered

2019-07-30

Start date

2019-08-01

Completion date

Unknown

Last updated

2019-08-27

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

Conditions

post-adolescene acne

Interventions

experimental group:strong pulsed light combined with supramolecular salicylic acid

control group:supramolecular salicylic acid

Eligibility

Sex/Gender

All

Age

25 Years to No maximum

Inclusion criteria

Inclusion criteria: Aged >= 25 years, male or female with acne vulgaris (light and moderate patients);

Exclusion criteria

Exclusion criteria: For external use or oral retinoids within 1 month; for external or oral steroids within 1 month; pregnant or lactating women; psychiatric patients; history of photosensitivity or keloids; systemic disease or serious Dermatological patients; those who are allergic to salicylic acid; those who do not follow the pilot program.

Design outcomes

Primary

Measure	Time frame
effective rate;	—

Countries

China

Contacts

Public ContactWeng Wenjia

Beijing You'an Hospital, Capital Medical University

wenjia988weng@163.com+86 18800166323

Outcome results

None listed

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