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Safety evaluation of novel shampoo

Safety evaluation of novel shampoo in patients with Dry skin disease including sebum deficiency eczema and atopic dermatitis - Safety evaluation of novel shampoo in patients with Dry skin disease including sebum deficiency eczema and atopic dermatitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000046661
Enrollment
40
Registered
2022-01-17
Start date
2022-01-24
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

Persons with mild to moderate dry skin disease(including sebum deficiency eczema and atopic dermatitis)

Interventions

Use of the test shampoo at least 4 days a week for 4 weeks

Sponsors

Medical Corporation Hokubukai Utsukushigaoka Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients with mild to moderate dry skin disease(including Sebum deficiency eczema and atopic dermatitis) 2.Patients with minor to moderate dry skin symptoms at the examination areas 3.Japanese men and women between the ages of 20 and 69 4.Patients giving written informed consent with his or her own will after receiving an adequate information about the test bath solution and aim of this study

Exclusion criteria

Exclusion criteria: 1.Patients with rashes at the examination areas that intervene the evaluation 2.Patients with rosacea-like dermatitis or with steroid skin disease 3.Patients who take or anticipate to take medicines that affect the study such as oral steroids, immunosuppresant 4.Those who used cosmetics or quasi-drugs for the same purpose (hair wash) as the test product on the test site 5.Pregnant women 6.Lactating women 7.Patients who have experienced severe skin symptoms many times due to the use of cosmetics in the past 8.Patients who are judged as inappropriate by principal investigator or sub-investigator with other reasons

Design outcomes

Primary

MeasureTime frame
Skin findings(1)and adverse events(2):dermatologist examination,questionnaire for skin condition and the impression of test bath solution,recording daily life (1)0 week,2 week,4 week (2)2 week,4 week

Secondary

MeasureTime frame
Improvement of dryness and desquamation(dermatologist examination,photographic recording) 0 week,2 week,4 week

Countries

Japan

Contacts

Public ContactTakuya Matsuda

Medical Corporation Hokubukai Utsukushigaoka Hospital Center for Clinical Pharmacology

matsuda@ughp-cpc.jp011-882-0111

Outcome results

None listed

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