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Evaluation of the anti-recurrence efficacy and safety of Bedar Antomint Moisturizing Cream in children with moderate atopic dermatitis: A randomized, double-blind, placebo-controlled multicenter clinical study

Evaluation of the anti-recurrence efficacy and safety of Bedar Antomint Moisturizing Cream in children with moderate atopic dermatitis: A randomized, double-blind, placebo-controlled multicenter clinical study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2600120490
Enrollment
Unknown
Registered
2026-03-16
Start date
2026-03-16
Completion date
Unknown
Last updated
2026-03-23

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

Conditions

Atopic dermatitis

Interventions

Control group:Placebo + topical glucocorticoid
The experimental group:Bedma Antomint Moisturizing Cream + Topical Corticosteroid

Sponsors

Beijing Childrens Hospital,Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 12 Years

Inclusion criteria

Inclusion criteria: 1. Ages 3 months to 12 years (inclusive of 3 months and 12 years); 2. Adhering to the Hanifin-Rajka AD diagnostic criteria, moderate atopic dermatitis subjects have an IGA score of 3, and the SCORAD score must be between 15 and 40; 3. The subjects and their guardians are willing to strictly follow the investigator's instructions to use the test product throughout the study period and refrain from using other similar products; 4. The guardians of the subjects agree to sign the informed consent form.

Exclusion criteria

Exclusion criteria: 1. There are other skin lesions in the study area besides atopic dermatitis; 2. Screening for those who have used systemic glucocorticoids, immunomodulators or immunosuppressants (excluding antihistamines) within 4 weeks before the assessment; 3. Screening for those who have received systemic treatment with JAK inhibitors/biological agents or other similar treatments within 6 months before the assessment; 4. The subjects have undergone general anesthesia surgery in the past month; 5. Screening for children who have participated in other clinical trials within 3 months before the assessment; 6. The eczema lesions of the subjects show exudation or any other signs of infection (such as pus, erosion, exudation, secondary infection, etc.); 7. Children who are known to be allergic to any component of the test product; 8. Children who, in the judgment of the investigator, are not suitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
Safety;The improvement effect of the test subject on the recurrence of atopic dermatitis in children;

Secondary

MeasureTime frame
Quality of life;Improvement of clinical symptoms;Subjective satisfaction of the tested item;

Countries

China

Contacts

Public ContactMa Lin

Beijing Childrens Hospital,Capital Medical University

malin@bch.com.cn+86 10 59616083

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Apr 3, 2026