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A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Trial to Evaluate The Effect of Edible Hyaluronic Acid of Cockscomb Origin on Atopic Dermatitis Patient

A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Trial to Evaluate The Effect of Edible Hyaluronic Acid of Cockscomb Origin on Atopic Dermatitis Patient - ADP-ECME-ad-01

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT1090220075
Enrollment
80
Registered
2011-12-16
Start date
2012-01-16
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

Atopic Dermatitis (AD)

Interventions

Intervention type: Name of intervention:ECM-E Dose form / Japanese Medical Device Nomenclature:TABLET Route of administration / Site of application:ORAL Dose per administration:900,1200 mg Dosing freq

Sponsors

ADAPTGEN PHARMACEUTICAL CO.LTD.
Lead Sponsor
Hirose Clinic,MEDOC Medical Dock&Clinic,Sanbongi Clinic
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: *Age: a patient who is 4 to 44 years old at the time of Informed Consent *Sex: don't ask *hospitalization and visitors *Disease: The patient who is diagnosed with atopic dermatitis based on the Japanese Dermatological Association atopic dermatitis clinical practice guideline and who wishes to treat or under medical treatment.

Exclusion criteria

Exclusion criteria: 1) - Contact dermatitis - Seborrheic dermatitis - Prurigo simplex - scabies - Heat rash - Fishskin disease - Leather fat deficiency eczema - Hand eczema (in order to except hand eczema other than atopic dermatitis), and a cutaneous lymphoma - Psoriasis - The disease by immunity deficiency - Collagen disease (SLE,Dermatomyositis) - Nether ton syndrome 2) Patient which have allergies in chicken 3)Mucopolysaccharidosis 4) The woman and nursing mother who wish to become pregnant during pregnancy or exam time 5)Those who have been suffered from critical liver and renal damage, and cardiac disease 6)The patient who has critical complications 7)Those who participated in other clinical tests within the past three months 8)The patient considered to be disqualified by judgment of the doctor who examines

Design outcomes

Primary

MeasureTime frame
The improvement evaluation of atopic dermatitis severity The improvement evaluation according to the judgment of the degree of itchy

Countries

Japan

Contacts

Public ContactToru Urakawa

ADAPTGEN PHARMACEUTICAL CO.LTD.

adurakawa@adaptgen.co.jp+81-572-56-1111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026