A Clinical Study to Assess the Safety, In-use Tolerabilit... | NCT06489600

NCT06489600

Protocol Section

Identification Module

Results Section

No data available

No data is available for this block.

Annotation Section

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No data is available for this block.

Document Section

No data available

No data is available for this block.

Derived Section

Miscellaneous Info Module

Status Module

Name	Class
Kayura Effects LLP	UNKNOWN

Description Module

Label	Type	Description	Intervention Names
No Rays, Thanks Mineral sunscreen	Experimental	Wash your face with standard facewash and apply a pea size amount on the face in the morning.	Other: No Rays, Thanks Mineral sunscreen

Name	Type	Description	Arm Group Labels	Other Names
No Rays, Thanks Mineral sunscreen	Other	Wash your face with standard facewash and apply a pea size amount on the face in the morning. Dosage form: semi-solid frequency: Once in a day Route of Administration: Topical

Outcomes Module

Primary Outcomes

Measure	Description	Time Frame
Change in local intolerance assessment for skin irritation using 4-point scoring scale where 0 indicate absent and 3 indicate severe.	To assess the safety of the test product in terms of change in local intolerance assessment for irritation by dermatological assessment	On Day 01 at T15 minutes and on Day 15 (± 2 Days).
Change in local intolerance assessment for skin dryness using 4-point scoring scale where 0 indicate absent and 3 indicate severe.	To assess the safety of the test product in terms of change in local intolerance assessment for dryness by dermatological assessment	On Day 01 at T15 minutes and on Day 15 (± 2 Days).
Change in local intolerance assessment for skin oedema using 4-point scoring scale where 0 indicate absent and 3 indicate severe.	To assess the safety of the test product in terms of change in local intolerance assessment for oedema by dermatological assessment	On Day 01 at T15 minutes and on Day 15 (± 2 Days).
safety of the test product in terms of local intolerance assessment of irritation (Patient Global Assessment scale) where 0 indicate not at all and 10 indicate very severe.	To evaluate the safety of the test product in terms of local intolerance assessment of irritation by Patient Global Assessment scale.	On Day 01 at T15 minutes and on Day 15 (± 2 Days).
safety of the test product in terms of local intolerance assessment of dryness (Patient Global Assessment scale) where 0 indicate not at all and 10 indicate very severe.	To evaluate the safety of the test product in terms of local intolerance assessment of dryness by Patient Global Assessment scale.	On Day 01 at T15 minutes and on Day 15 (± 2 Days).

Secondary Outcomes

Measure	Description	Time Frame
where will you rank the test product in terms of appearance in which 1 indicate very poor and 5 indicate excellent.	To assess the test product in terms of change in organoleptic parameters- appearance through the subject product perception assessment.	On Day 01 and after test product usage on Day 01 at T15 minutes, and on Day 15 (±2 Days)

Eligibility Module

Eligibility Criteria

Inclusion Criteria:

Age: 18 to 55 years (both inclusive) at the time of consent.
Sex: Healthy male and non-pregnant/non-lactating females. (Preferably equal ratio of males and females)
Females of childbearing potential must have a self-reported negative pregnancy test.
Subject are generally in good health.
Subject with dry and sensitive skins. (As per the dermatological evaluation).
Subject is able to remain on stable doses of contraceptive or replacement hormonal therapy, including no therapy, 6 weeks prior to and for the duration of the study.
If the subject is of childbearing potential, is practicing and agrees to maintain an established method of birth control (IUD, hormonal implant device/injection, regular use of birth control pills or patch, diaphragm, condoms with spermicide or sponge with spermicidal jelly, cream or foam, partner vasectomy or abstinence). Females will be considered as non-childbearing potential if they are surgically sterile, have been post-menopausal for at least 1 year or have had a tubal ligation.
Subjects are willing to give written informed consent and are willing to come for regular follow up.
Subjects who commit not to use medicated skincare products other than the test product for the entire duration of the study.
Subject who have not participated in a similar investigation in the past three months.
Willing to use test product throughout the study period.

Exclusion Criteria:

History of any dermatological condition of the skin disease.
Subject with present condition of allergic response to any cosmetic product.
Subjects under chronic medication (e.g. aspirin-based products, anti-inflammatories, anti-histamines, corticotherapy etc.) that might influence the outcome of the study.
History of alcohol or drug addiction.
The subject has clinically significant skin disease, which may contraindicate participation, including psoriasis, eczema, skin cancer or other skin pathology.
Subjects having skin infections like bacterial, fungal, viral infections.
The subject has skin irritation, open wounds, cuts, abrasions, irritation symptoms or any dermatological condition on the face that can interfere with the reading.
Be wearing any facial makeup, including false eyelashes, on the day of the study visit.
Subjects having hypersensitive skin.
Subjects using other marketed sun screen products during the study period.
Any other condition which could warrant exclusion from the study, as per the dermatologist's/investigator's discretion.
Pregnant or breastfeeding or planning to become pregnant during the study period.
History of chronic illness which may influence the cutaneous state.
Subjects participating in other similar cosmetics, devices or therapeutic trials or skincare products within the last four weeks.

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