To evaluate the safety and efficacy of Plum serum in Hair Growth

Not Applicable

• Registration Number: CTRI/2024/02/062978
• Lead Sponsor: Pureplay Skin Sciences India Pvt Ltd

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 4 March 2024

Recruitment & Eligibility

• Status: Open to Recruitment
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

1. Indian or Asian female and male subjects with max Female : Male Ratio – 80:20 with Stage 2 and 3

2. Healthy subjects (no infectious and evolutive

pathology which could make the subject

vulnerable and stop the study, no pathology

which could interfere with the study, no

symptomin the process of an exploratory

checkup)

3. Between 25 and 40 years of age.

4. Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar….)

Exclusion Criteria

• Being pregnant or breastfeeding or having stopped to breastfeed in the past three months

• Having refused to give her assent by not signing the consent form

• Taking part in another study liable to interfere with this study

• Having a chronic dermatosis liable to modify the

cutaneous reactivity on the tested area

• Being insulin-dependent diabetic or non insulindependent diabetic with a recent therapy (less

than 6 months)

• Having a progressive asthma (either under

treatment or last fit in the last 2 years)

• Being epileptic

• Having non stabilized thyroid problems

(requirement of a stabilized treatment for at

least 6months)

• Having cutaneous hypersensitivity

• Having a diagnosed or highly probable allergy

to one or several compounds of the cosmetic

products

• Following a chronic or intermittent medicinal

treatment comprising any of the following

products : aspirin-based products, antiinflammatories, anti-histamines, anti-coagulants, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol)

• Having undergone a surgery requiring a general

anaesthetic of more than one hour in the past6

months

• Having changed her cosmetic habits except

those required by the protocol in the 14

dayspreceding the start of the study on the

studied anatomic unit

• Having applied a cosmetic product on the

studied areas the first day of the study (except

theusual shampoo)

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Change in Hair growthTimepoint: T0min, T+2 days, T+28 days ,T+30 days, T+56 days T+58 <br/ ><br>days, T+84 days and T+86 days

Secondary Outcome Measures

Name	Time	Method
ot ApplicableTimepoint: Not Applicable