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Clinical study on the improvement of atopic dermatitis recurrence

Clinical study on the improvement of recurrence of atopic dermatitis by Longmu Cream Formula

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400079579
Enrollment
Unknown
Registered
2024-01-06
Start date
2024-01-06
Completion date
Unknown
Last updated
2024-01-14

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:Longmu Cream Formula
control group:placebo

Sponsors

Xiyuan Hospital of Chinese Academy of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
6 Years to 12 Years

Inclusion criteria

Inclusion criteria: (1) Comply with the Chinese and Western medical diagnostic criteria and evidence criteria of AD; (2) The degree of disease is mild to moderate patients; (3) Aged 6-12 years old; (4) Patients or their guardians signed the informed consent and had good compliance.

Exclusion criteria

Exclusion criteria: (1) Have received AD-related topical, oral, or systemic therapy, such as topical calcineurin inhibition, within one week; (2) Abnormal liver or kidney function (ALT, AST greater than 1.5 times, BUN, Cr greater than 1 times) or suffering from other other serious diseases; (3) Combination of other dermatological diseases that affect the judgement of the severity of the disease; (4) Known history of allergy to the test drugs (drugs in Longmu Cream Formula); (5) Patients who are also participating in other clinical trials.

Design outcomes

Primary

MeasureTime frame
eczema area and severity index;

Secondary

MeasureTime frame
peak pruritus numerical rating scale;the Children’s dermatology life quality index;patient-oriented eczema measure;RECAP of atopic eczema;Inflammatory indicators;Histological index;

Countries

China

Contacts

Public ContactLang Na

Xiyuan Hospital of Chinese Academy of Traditional Chinese Medicine

langna96@126.com+86 136 6114 0663

Outcome results

None listed

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