Skip to content

A multicenter, randomized, double-blind, parallel controlled clinical study on the efficacy and safety of Hydebao Capustat mussel ceramide moisturized body emulsion in the treatment of mild atopic dermatitis

A multicenter, randomized, double-blind, parallel controlled clinical study on the efficacy and safety of Hydebao Capustat mussel ceramide moisturized body emulsion in the treatment of mild atopic dermatitis

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087274
Enrollment
Unknown
Registered
2024-07-24
Start date
2024-05-14
Completion date
Unknown
Last updated
2024-07-29

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

Conditions

Atopic dermatitis

Interventions

Trial group: Hydebao Capstock Mussel ceramide Double Moisturize Body Care Lotion:Hyderberg Capstein Mussel ceramide Double Moisturizing Body Lotion
Control group
Hydebao Capstax Mussel ceramide Bihydrin Body Care Lotion matrix:Blank matrix

Sponsors

Shanghai Dermatology Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 55 Years

Inclusion criteria

Inclusion criteria: a. Meet the Williams diagnostic criteria for atopic dermatitis; b. Any gender, age 18-55 years old; c. The target lesion is 2-10 cm in diameter, located on the limbs or trunk; d. Mild atopic dermatitis with eczema area and severity index (EASI)=6 points; e. Lesion area < 5% body surface area before treatment (assessed according to the palm method, 1% based on the patient's palm area); f. Sign informed consent, voluntarily participate in this project, and insist on regular follow-up as required.

Exclusion criteria

Exclusion criteria: a. Pregnant or lactating women; b. Received AD systemic therapy within three months and local therapy or phototherapy within the last two weeks; c. Have serious heart, lung, gastrointestinal, liver, kidney and other systemic diseases or mental diseases; d. Allergic to calcium preparations; e. Have a systemic or active skin disease (e.g., psoriasis) that may affect the evaluation of the test results; f. Patients with scars, birthmarks, tattoos, sun spots, etc. in the affected area that may affect the evaluation of skin lesions; g. Patients with bacterial, viral or fungal infections requiring anti-infective therapy; h. Patients who have participated in or are participating in a clinical study of another investigational drug within one month; i. Investigators with communication barriers who could not complete the questionnaire independently.

Design outcomes

Primary

MeasureTime frame
Effective after 2 weeks of treatment;

Secondary

MeasureTime frame
Eczema Area and Severity Index (EASI) score;Therapeutic effectiveness;Visual analogue scale (VAS);The investigator's global assessment (IGA);Dermatology life quality index (DLQI);Take pictures of the affected area;

Countries

China

Contacts

Public ContactLi Bin/Wang Ruiping

Shanghai Dermatology Hospital

w19830901@126.com+86 138 1684 5803

Outcome results

None listed

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