A verification study of the test product of skin improvement effect by application of test product

A verification study of the test product of skin improvement effect by application of test product: an open-label study - A verification study of the test product of skin improvement effect by application of test product

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000051441

Enrollment

Registered

2023-06-23

Start date

2023-06-23

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

Healthy Japanese subjects

Interventions

Duration: Four weeks Test product: Moringa seed oil Administration: Apply the test product to the elbow, knee, and heel on the side of the dominant hand&#39

s side. Don&#39

t use the test product or other skin care products on the other side.

Eligibility

Sex/Gender

Female

Inclusion criteria

Inclusion criteria: 1. Japanese 2. Women 3. Adults 4. Healthy subjects

Exclusion criteria

Exclusion criteria: 1. Subjects who are undergoing medical treatment or have a medical history of malignant tumor, heart failure, and myocardial infarction 2. Subjects who have a pacemaker or an implantable cardioverter defibrillator (ICD) 3. Subjects currently undergoing treatment for any of the following chronic diseases: cardiac arrhythmia, liver disorder, kidney disorder, cerebrovascular disorder, rheumatism, diabetes mellitus, dyslipidemia, hypertension, or any other chronic diseases 4. Subjects who use or take "Foods for Specified Health Uses," or "Foods with Functional Claims" in daily 5. Subjects who are currently taking medications (including herbal medicines) and supplements 6. Subjects who are allergic to medicines and/or the test product related products 7. Subjects who have a medical history of allergy due to using cosmetics 8. Subjects who have inflammation symptoms at the site of application (elbow, knee, or heel) 9. Subjects who use skincare products on the site of application (elbow, knee, or heel) or receive skincare treatment during this trial 10. Subjects who are pregnant, lactating, or planning to become pregnant during this trial 11. Subjects who have been enrolled in other clinical trials within the last 28 days before the agreement to participate in this trial or plan to participate another trial during this trial 12. Subjects who are judged as ineligible to participate in this study by the physician

Design outcomes

Primary

Measure	Time frame
1. The transepidermal water loss, moisture content of skin, skin viscoelasticity of elbows, knees and heels	—

Countries

Japan

Contacts

Public ContactNaoko Suzuki

ORTHOMEDICO Inc. R&D Department

nao@orthomedico.jp03-3818-0610

Outcome results

None listed

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