72 hour moisturization study of Plum Oat & Allantoin All-day Nourishing Cream

A Clinical Study to evaluate the 72 hour moisturization potential of Plum Oat & Allantoin All-day Nourishing Cream. - NIL

Status

Recruiting

Phases

Phase 4

Study type

Interventional

Source

CTRI

Registry ID

CTRI/2023/11/059540

Enrollment

Registered

2023-11-06

Start date

Unknown

Completion date

Unknown

Last updated

2024-01-22

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

Conditions

None listed

Interventions

Intervention1: Oat & Allantoin All-day Nourishing Cream: Route of administration: Topical, Frequency :2-3gm cream over one hand, Duration: 72 hours Control Intervention1: Not applicable: Not applicabl

Eligibility

Inclusion criteria

Inclusion criteria: 1) Gender: Male or Female 18 to 50 2) Subjects willing to give written informed consent 3) Women of child bearing potential must have a negative urine pregnancy test prior to study entry. 4) Are free of any systemic or dermatologic disorder, which, in the opinion of the investigator, will interfere with the study results or increase the risk of adverse events. 5) Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial) for the duration of the study.

Exclusion criteria

Exclusion criteria: 1. Subjects who are pregnant, breast-feeding, or planning to become pregnant during the study. 2. Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years, or any other confounding skin condition. 3. Have open sores or open lesions in the treatment area(s). 4. Have any condition that, in the opinion of the investigator, would confound the safety and/or efficacy assessments of the product. 5. Have participated in any interventional clinical trial in the previous 90 days. 6. Have a known sensitivity to any of the constituents of the test product including sensitivities to Helianthus Annuus, Avena Sativa (Oat) Kernel, Argania Spinosa. 7. Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e., biologics), including corticosteroids. 8. Have not skin related issues

Design outcomes

Primary

Measure	Time frame
change in the moistureTimepoint: T0min, T+30 mins, T+ 2 hours, T+4 hours, T+ 8 hours, T+24 hours, T +48 hours, T + 72 hours	—

Secondary

Measure	Time frame
Total Epidermal Water LossTimepoint: 0 Hr, 24 Hr, 48 Hr, 72 Hr	—

Countries

India

Contacts

Public ContactPuneet Mittal

CCFT Laboratories

puneetmittal@mgcts.org8937015757

Outcome results