Skip to content

Safety evaluation of Lip care formulation

Evaluation of irritation potential of Lip Care formulation on healthy human subjects. - NIL

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2023/08/056024
Enrollment
26
Registered
2023-08-02
Start date
Unknown
Completion date
Unknown
Last updated
2023-11-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

None listed

Interventions

Intervention1: Little Joys Lip balm: Approximately 0.04 ml (40 µl) of test product will be transfer on Aluminium Finn Chamber with the loaded product will then be taped onto the back of subjects for 2

Sponsors

MOSAIC WELLNESS PRIVATE LIMITED
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Standard criteria -Asian Indian male and female subjects. -Healthy human 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 symptom in the process of an exploratory check-up) -Between 18 and 65 years of age. -Skin is healthy on the studied anatomic unit (free of eczema, wounds, inflammatory scar….)

Exclusion criteria

Exclusion criteria: 1.Standard 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, antihistamines, 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 a diagnosed or highly probable allergy to one or several compounds of the cosmetic products. -Having undergone a surgery requiring a general anaesthesia 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. -The day of the patch application: no cosmetic product must be used (test site clean with water only). 2.Refusing to follow the restrictions below during the study: - For female: Do not become pregnant nor breastfeed. - Do not take part in another study liable to interfere with this study. - Do not take medicinal treatment comprising any of the following products: aspirin-based products, anti-inflammatories, and antihistamines, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol). - Do not change his/her cosmetic habits apart from the particular conditions mentioned in the protocol, on the studied anatomic unit 3.Specific criteria -Having eczema, psoriasis, lichen plan, vitiligo whatever the considered area. -Having disorder of the healing (whatever the considered area) -Having a rhinitis, allergic conjunctivitis or rhino sinusitis -Having an allergy to perfumes and/or preservatives in cosmetic products. -Having an allergy to plaster -Having a food allergy -Having a cardiovascular pathology (taking a beta blocker treatment) -Having immunosuppressive drugs, such as cyclophosphamide, methotrexate, azathioprine, etc. -Taking a retinoid-based treatment by general or oral route -Taking specific treatment on the back. -Having taken an anti-histaminic treatment in the last 2 weeks preceding the start of the study -Having miliaria (prickly heat) on the back. -Presenting too many naevus on the back -Having high pilosity on the back. 4.Refusing to follow the restrictions below during the study: - During the first 24 hours (after patch application), neither cosmetic products nor water must be applied on the back. - Till the follow up period of until T8 days, only water is accepted from the first reading i.e., T2 days (24 hours after the patch removal). - Do not practice an intensive sport activity during the first 24 hours (until the removal of the patches) - Do not expose the back to the sun.

Design outcomes

Primary

MeasureTime frame
Dermatological safety / Irritation potential on skinTimepoint: Baseline, 0 hr , 24 hours & day 7

Secondary

MeasureTime frame
NILTimepoint: NOT APPLICABLE

Countries

India

Contacts

Public ContactDr Mohit Lalvani

MASCOT-SPINCONTROL India Pvt. Ltd.

raji@mascotspincontrol.in02243349191

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Feb 4, 2026