MedPath

Effect of product on pimple spots

Not Applicable
Conditions
Health Condition 1: L819- Disorder of pigmentation, unspecified
Registration Number
CTRI/2024/08/072028
Lead Sponsor
Onesto Labs Pvt. Ltd.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Yet Recruiting
Sex
Not specified
Target Recruitment
0
Inclusion Criteria

1.Indian female subjects.

2.Healthy subjects

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

4.Having hyperpigmentation (Acne PIH) dark spot

Exclusion Criteria

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

• Having refused to give her assent by 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-insulin-dependent 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 6

months).

• Having cutaneous hypersensitivity

• Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic

products or food products or to latex

• Having known allergy to any of the Ingredient of the Test Product.

• 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 undergone a surgery requiring a general anaesthetic of more than one hour in the past 6

months.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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