CTRI/2024/01/061163CompletedPhase 4
A Clinical Study to evaluate the 8-hour moisturization potential of Multiple Saliguard Samples at concentration 3%. - NI
Salicylates & Chemicals Pvt. Ltd.0 sites0 target enrollmentStarted: TBDLast updated:
Trial Snapshot
- Phase
- Phase 4
- Status
- Completed
- Sponsor
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
Inclusion Criteria
- •1) Gender: Male or Female with age 18-40
- •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
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 efficacy assessments of the
- •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.
- •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
Investigators
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