None listed
Conditions
Interventions
Intervention1: Test Product: 20% Urea Foot Roll On: Take approx. 1.0 ml quantity of test product. Application: twice a day, Route of administration: Topical, Duration: 2 week
Control Intervention1: No
Sponsors
Mosaic Wellness Pvt. Ltd
Eligibility
Inclusion criteria
Inclusion criteria: 1. Gender: Male or Female 18 to 65 2. Subjects willing to give written informed consent 3. Subjects having Cracked Heals 4. Subjects having diabetic and non-diabetic. 4. Women of child bearing potential must have a negative urine pregnancy test prior to study entry. 5. 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. 6. Are willing to avoid prolonged exposure of the treatment area to ultraviolet radiation (natural or artificial)
Exclusion criteria
Exclusion criteria: 1. Subjects who are pregnant, breast-feeding, or planning to become 2. pregnant during the study. 3. Have any evidence of systemic cancer, squamous cell carcinoma, basal cell carcinoma, in the last 5 years, or any other confounding skin condition. 6. Have any condition that, in the opinion of the investigator, would confound the safety and/or efficacy assessments of the product. 7. Have participated in any interventional clinical trial in the previous 90 days. 8. Have a known sensitivity to any of the constituents of the test product 9. Have used, are using, or are planning to use immunosuppressive or immunomodulatory medication (i.e., biologics), including corticosteroids
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Change in Hydration Change in Craked Heels Change in Smoothness Change in Softness Timepoint: At T0min, T+1hrs, T+7days, T+14days | — |
Secondary
| Measure | Time frame |
|---|---|
| Not ApplicableTimepoint: Not Applicable | — |
Countries
India
Contacts
Public ContactPuneet Mittal
CCFT Laboratories
Outcome results
None listed