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A using test for four continuous weeks of C-271 in babies

A using test for four continuous weeks of C-271 in babies - A using test for four continuous weeks of C-271 in babies

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000038263
Enrollment
60
Registered
2021-08-06
Start date
2020-02-06
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

None listed

Interventions

Examination on screening visit - Use the test sample on the whole body for two weeks - Examination such as observation and measurement on after two weeks visit - Use the test sample on the whole body

Sponsors

Inforward, inc EBISU skin research center
Lead Sponsor
CliniPro Co., Ltd.
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Subjects who is satisfying all of the following criteria. 1)Healthy babies (male and female) aged 28 days-old to 11 months-old. 2)Subjects' protectors (parents or guardians) who are able to show their willingness of participating to the test, and to sign the consent form after understanding details of the test. 3)Subjects and their protectors who can manage in persion visit for all required visits.

Exclusion criteria

Exclusion criteria: 1)Premature babies. 2)Subjects with birth weight <2,500g. 3)Subjects who have severe eczema infantile. 4)Subjects who have skin symptom such as atopic dermatitis. 5)Subjects who have trauma on the part that uses the test sample. 6)Subjects who have possibility to be exposed to many quantity of sunlight during implementing the test. 7)Subjects who are participating in clinical tests and use tests that apply cosmetic, quasi-drugs and others. 8)Subjects who have allergic symptoms against external medicine, cosmetic, quasi-drugs and others in the past. 9)Subjects who have medical history of serious liver dysfuction, kidney dysfuction and myocardial infarction. 10)Subject who are visiting the hospital regulary for receiving the medical treatment due to the diseases. 11)Subjects who have their family they are working at cosmetic companies and pharmaceutical companies. 12)Others, subjects who have been determined that he/she is ineligible by investigators.

Design outcomes

Primary

MeasureTime frame
Changes over time of the systemic skin, between screening visit and after four weeks visit, observed by the Investigators, such as dryness or scale, desquamation, erythema, papules, scratch mark, feeling of stimulation and pruritus.

Secondary

MeasureTime frame
* Changes over time of the systemic skin, between screening visit and after two weeks visit, observed by the Investigators, such as dryness or scale, desquamation, erythema, papules, scratch mark, feeling of stimulation and pruritus. * Changes over time of the quantity of stratum corneum water content and transepidermal water loss between screening visit, after two weeks visit and after four weeks visit.

Countries

Japan

Contacts

Public ContactKanako Sakurai

Inforward, inc EBISU skin research center

sakurai@inforward.co.jp03-5793-8712

Outcome results

None listed

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