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LA ROCHE POSAY EFFACLAR DUO+ for Mild to Moderate Acne Treatment Efficacy and Safety Study

LA ROCHE POSAY EFFACLAR DUO+ for Mild to Moderate Acne Treatment Efficacy and Safety Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100051398
Enrollment
Unknown
Registered
2021-09-23
Start date
2020-07-21
Completion date
Unknown
Last updated
2022-06-20

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

Conditions

Acne

Interventions

Group A:DUO+ treatment alone
Group B:Duo+ combined with BPO treatment
Group C:BPO treatment alone

Sponsors

Shanghai Dermatology Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Adults 18~35 years old; 2.Facial skin lesions, mainly in patients with acne vulgaris, mild to moderate; 3.Mainly manifested as acne and inflammatory papules; 4.The patients voluntarily participated in clinical observation and signed an informed consent form. Willing to cooperate with follow-up observation. Have good communication and understanding skills.

Exclusion criteria

Exclusion criteria: 1. Patients with severe acne with pustules, cysts, nodules and other skin lesions on the face; 2. Other drugs and treatments for external use within one month; 3. Systematic treatment within three months (retinoic acid drugs and photodynamics within 6 months); 4. Use topical acne treatment drugs or functional skin care products one week before enrollment; 5. The affected area is complicated by other skin diseases that may obviously affect the efficacy evaluation; 6. Related diseases treated with female patients using estrogen or estrogen-like hormones; 7. Those who have a history of allergies to the medicines and ingredients used this time; 8. People with severe heart, brain, lung, liver, and kidney damage; 9. Pregnant women, breastfeeding women; 10. People with a history of psychological and mental illness, recent history of alcohol or drug abuse; 11. Patients who are unwilling to sign informed consent, and those who are unwilling to cooperate.

Design outcomes

Primary

MeasureTime frame
Changes in the number and severity of acne and inflammatory papules;

Secondary

MeasureTime frame
Erythema after inflammation;Melanin;Transdermal water loss;

Countries

China

Contacts

Public ContactShen Zhong

L'Oreal (China) Co., Ltd.

nancy.shen2@loreal.com+86 21-5200 7425

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 12, 2026