Evaluation of irritation potential of Skin Care Formulations on healthy human subjects having Varied skin types
Trial Snapshot
- Phase
- Not Applicable
- Status
- Not yet recruiting
- Sponsor
- Enrollment
- 26
- Locations
- 1
- Primary Endpoint
- Dermatological safety / Irritation potential on skin
Study Overview
Brief Summary
Objective: The objective of this study will be to evaluate the irritation potential on healthy human subjects having Varied skin types of Skin Care Formulation
Duration of study: 8 days study
Kinetics: T0 (Evaluation of test sites by Dermatologist, Patch application) ,T1(Patch removal, Evaluation of test sites by Dermatologist ,T2(Evaluation of test sites by Dermatologist and Subject post 24 hrs of patch removal), T8 (Evaluation of
test sites by Dermat and Subject post 1 week of patch removal and tracking the positive cases)
Population: 26 healthy subjects (13 males + 13 females) with varied skin types.
The test area is checked for erythema and oedema caused due to the products and compared with positive control
Study Design
- Study Type
- Interventional
- Allocation
- Na
- Masking
- Participant Blinded
Eligibility Criteria
- Ages
- 18.00 Year(s) to 65.00 Year(s) (—)
- Sex
- All
Inclusion Criteria
- •Healthy Human Subjects 2) Skin should be healthy on the studied anatomic unit 3)Subjects representing varied skin types.
Exclusion Criteria
- •For female: Being pregnant or breastfeeding or having stopped to breastfeed in the past three months.
- •Having refused to give his/her assent by not signing the consent form.
- •Taking part in another study liable to interfere with this study.
- •Being diabetic.
- •Being asthmatic.
- •Following a chronic medicinal treatment comprising any of the following products: aspirin-based products, anti-inflammatories, anti-histamines, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol).
- •Having cutaneous hypersensitivity (except in the case of studies with evaluation of sensitive skin).
- •Having undergone a surgery requiring a general anesthesia of more than one hour in the past 6 months.
- •Having changed his/her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit.
Outcomes
Primary Outcomes
Dermatological safety / Irritation potential on skin
Time Frame: Baseline,0 hrs,24 hrs and 7 days
Secondary Outcomes
No secondary outcomes reported
Investigators
Dr Pooja Yadav
MASCOT-SPINCONTROL India Pvt. Ltd.