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Use of Mometasone Furoate plus Moisturizer for the Treatment of Atopic Dermatitis/Non-Wet(sicca) Eczema:A multicenter and controlled clinincal trial

Guideline-oriented Research in the Management of Some Common and Severe Skin Diseases

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003551
Enrollment
Unknown
Registered
2013-09-03
Start date
2011-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

Atopic Dermatitis/Non-Wet(sicca) Eczema

Interventions

Mometasone Furoate Group:Topical use Mometasone Furoate,once per day
Mometasone Furoate plus Moisturizer Group:Use Mometasone Furoate, once per day
Use Moisturizer, once per day

Sponsors

Institute of dermatology, Chinese Academyof Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
2 Years to 80 Years

Inclusion criteria

Inclusion criteria: (1) Males and females aged between 2 and 80 years; (2) Atopic Dermatitis/Non-Wet(sicca) Eczema defined by the Diagnostic criteria; (3) SCORAD<30; (4) Provide written informed consent and Willing and able to comply with all aspects of the protocol. If Under 18 years old, informed consent will be written by the legal guardian.

Exclusion criteria

Exclusion criteria: (1) Requires the system medication to control the disease; (2) Patients with skin lesions associated with other diseases that may affect the curative effect judgment; (3) Systemic biologic therapies within 4 weeks prior to randomization; (4) Ultraviolet therapy within 4 weeks prior to randomization; (5) Plan to use the following drugs, such as corticosteroids, antibiotics, immunosuppressants, immunomodulators agents, which may affect the efficacy evaluation during the study period; (6) patients who are allergic to any ingredient of the drug to be studied; (7) Pregnant or lactating females; (8) Any other situations not suitable for this study determined by the investigators.

Design outcomes

Primary

MeasureTime frame
Recurrence rate;Median time to recurrence;SCORAD score;Eosinophil count;

Countries

China

Contacts

Public ContactBaoxi Wang

Institute of Dermatology, Chinese Academy of Medical Sciences

wangbx@ncstdlc.org+86 025-85478071

Outcome results

None listed

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