Skin Irritation test on Kapiva Skin Ritual Kumkumadi Glow Face Oil
Recruiting
- Conditions
- Not applicable. This is a Irritation Patch Test Study
- Registration Number
- CTRI/2023/08/056692
- Lead Sponsor
- Adret Retail Pvt Ltd
- Brief Summary
**The below products would be tested as per the guideline IS4011 for dermal safety assessme****nt.**
1. Kapiva Skin Ritual Kumkumadi Glow Face Oil
The product will be tested for skin irritation on 24 human volunteers.
Assessment would be done on day 0, day 1, with followup visit on day 8 for erythema and Oedema scoring.
Study is done as per BIS standard 4011
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- All
- Target Recruitment
- 24
Inclusion Criteria
- Voluntary male/women between 18 and 65 years.
- Photo type III to V.
- Having apparently healthy skin on test area 4.
- For whom the investigator considers that the compliance will be correct.
- Cooperating, informed of the need and duration of the examinations and ready to comply with protocol procedures.
- Having signed a Consent Form.
- Willingness to avoid intense UV exposure on test site (sun or artificial UV), during the course of the study.
- Willingness to avoid excessive water contact (for example swimming) or activity which causes excessive sweating (that is exercise, sauna…), during the course of the study.
- Should be able to read and write (in English, Hindi or local language).
- Having valid proof of identity and age.
Exclusion Criteria
- Pregnant/nursing mothers 2.
- Scars, excessive terminal hair or tattoo on the studied area.
- Henna tattoo anywhere on the body (in case of studies involving hair dyes).
- Dermatological infection/pathology on the level of studied area.
- Hypersensitivity, allergy antecedent (to any cosmetic product, raw material or hair dye).
- Any clinically significant systemic or cutaneous disease, which may interfere with study treatment or procedures.
- Chronic illness which may influence the outcome of the study.
- Subjects on any medical treatment either systemic or topical which may interfere with the performance of the study treatment (presently or in the past 1 month).
- Subject in an exclusion period or participating in another food, cosmetic or therapeutic trial.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Change in Skin Irritation Score-erythema & oedema Day 1, Day2 , Day8
- Secondary Outcome Measures
Name Time Method Not applicable Not applicable
Trial Locations
- Locations (1)
CCFT laboratories, AR multispecialty hospital and research center
🇮🇳Meerut, UTTAR PRADESH, India
CCFT laboratories, AR multispecialty hospital and research center🇮🇳Meerut, UTTAR PRADESH, IndiaDr Robin ChughPrincipal investigator7078103723robinderm25@gmail.com