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A 12 week, randomized, double-blind, placebo-controlled clinical trial for the evaluation of the efficacy and safety of TabetriTM on atopic dermatitis in children

A 12 week, randomized, double-blind, placebo-controlled clinical trial for the evaluation of the efficacy and safety of TabetriTM on atopic dermatitis in children

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
CRIS
Registry ID
KCT0002640
Enrollment
60
Registered
2018-01-09
Start date
2017-12-29
Completion date
Unknown
Last updated
2019-03-11

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

Conditions

None listed

Interventions

Dietary Supplement : In case of experimental group, TabetriTM (10g/pack), a stick jelly type, is orally administered after meal (morning and evening), taken 1 pack at a time, twice a day for 12 weeks.

Sponsors

Nutri Biotech
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Patients who agree to participate in this experiment and write consent including the subject and the parent (or legal representative) 2) Patients who aged 4~12 years of both sexes 3) Patients who have had intermittent or persistent atopic dermatitis symptoms for more than 6 months 4) Patients with mide to moderate atopic dermatitis symptoms (SCORing of Atopic Dermatitis, SCORAD index range from 20 to 50)

Exclusion criteria

Exclusion criteria: 1) Pateints who had severe skin disease, systemic disease 2) Patients who had prior treatments associated with atopic dermatitis, including systemic antibiotics, corticosteroids, anti-histamines, immunosuppressant within 4 weeks prior to the study 3) Patients who administered medicine, herbal medicine, any health functional supplements to improve atopic dermatitis within 1 week 4) Patients who had phototherapy within 4 weeks prior to the study 5) Patients who plan to participate in another human body test during this experiment 6) Patients who participated in another human body test before this experiment within 4 weeks 7) Patients who is deemed by the examiner to be inappropriate for this experiment

Design outcomes

Primary

MeasureTime frame
SCORAD total score

Secondary

MeasureTime frame
SCORing of Atopic Dermatitis objective score;SCORing of Atopic Dermatitis subjective score;Investigator’s Global Assessment;Eosinophil count, inflammatory biomarker;Usage of topical steroids (Percentage and dose)

Countries

Korea, Republic of

Contacts

Public ContactHye Jin Shin

Kyung Hee University Oriental Medicine Hospital at Gangdong

jame0130@naver.com+82-2-440-7127

Outcome results

None listed

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