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A study to evaluate the Moisturization Properties of Test Products.

A Single Center, Application Site Randomized, Blinded, Moisturization Study to Evaluate the Moisturization Properties of Test Products in Healthy Adult Human Participants. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2025/07/090037
Enrollment
36
Registered
2025-07-02
Start date
Unknown
Completion date
Unknown
Last updated
2025-07-21

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

Conditions

None listed

Interventions

Intervention1: Everyuth Naturals Body Lotion Rejuvenating Flora (New): Approx. 50 mg, Neat, Single application on volar forearms Intervention2: Everyuth Naturals Body Lotion Suncare Berries SPF 15

Sponsors

Zydus Wellness Products Limited,
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Healthy males and non-pregnant/non-lactating females (Preferably equal ratio) with age 18 to 50 years (both inclusive at the time of consent). 2. Participants having good general health as determined by the Investigator on the basis of medical history. 3. Female participants of childbearing potential must have a negative urine pregnancy test performed at enrollment visit. 4. Participants willing to abstain from using any cosmetic product on test sites, during the course of the study.

Exclusion criteria

Exclusion criteria: 1. Participants using Body milk /lotion / cream, cosmetics or any other body moisturizing product 3-5 days prior to study. 2. Participants who are on systemic medication or any medications would compromise the study. 3. Chronic illness which may influence the cutaneous state. 4. Participant having skin irritation, blemishes, excessive hair, moles, pigmentation, pimples, marks (e.g., tattoos, scars, and sunburn), open wounds, cuts, abrasions, irritation symptoms or any dermatological condition on the test site(s) i.e., volar forearm that can interfere with the reading. 5. Participants with known allergy or sensitivity to cosmetic products and/or any ingredients of the test product.

Design outcomes

Primary

MeasureTime frame
Instrumental and Dermatological AssessmentTimepoint: Day 01 [(Before application (i.e., baseline)] and after application at 30 mins(+05 mins) and 06 hours (+15 mins)] and 12 hours (+15 mins) on Day 01, on Day 02 [24 hours (+15 mins) and 36 hours (+15 mins) after application] and on Day 03 [48 hours (+15 mins) after application]

Secondary

MeasureTime frame
Subjective EvaluationTimepoint: Day 01 [30 mins(Plus 05 mins) after application] and Day 03 [48 hours (Plus 15 mins) after application]

Countries

India

Contacts

Public ContactDr Parth Joshi

Cliantha Research

ssethi@cliantha.com9825784942

Outcome results

None listed

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