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Will these 18 beauty products irritate your skin? a patch test seeks answers

NCT ID NCT07109453

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed This study
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Aug 07, 2026 · Last updated Aug 07, 2026

Summary

This trial checks whether 18 cosmetic products—including gels, creams, serums, toners, sunscreens, and hair care items—are safe for the skin. Healthy adults aged 18 to 65 with normal or sensitive skin will have small patches containing each product applied to their backs for 24 hours. Researchers will then look for any signs of redness or irritation, rating reactions on a scale from no reaction to severe. The goal is to see if these products are gentle enough for everyday use.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
18 cosmetic test products (gels, creams, serums, toners, sunscreens, hair products, face washes) applied to the skin via patch test
What this could lead to
If these products pass the patch test, they may be considered safe for use on sensitive skin, supporting their availability as gentle cosmetic options.
What could go wrong
This is a small early-stage safety study, not a test of effectiveness. Some people may still experience skin irritation despite the results.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

26 people

The number who actually took part.

Started

Aug 2025

Finished

Sep 2025

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 to 65 years

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria * Age: 18-65 years (both inclusive) at the time of consent. * Sex: Males and non-pregnant/non-lactating females (preferably equal number of males and females). * Subject with normal Fitzpatrick skin type III to V (Human skin colour determination scale). * Females of childbearing potential must have a self-reported negative pregnancy test. * Subject who do not have any previous * history of adverse skin conditions and are not under any medication likely to interfere with the results. * Subject is in good general health as determined by * the Investigator on the basis of medical history. * Subjects is willing to maintain the test patches in designated positions for 24 Hours. * Subject is willing and able to follow the study directions, to participate in the study, returning for all specified visits. * Subject must be able to understand and provide written informed consent to participate in the study. * Subject is willing to refrain from vigorous physical exercise during the study period and follow all the instruction given. * For Sensitive Skin Condition Only: * Subject scoring greater than 30 for Section 2 - Sensitive v/s Resistant skin in modified Dr Baumann's\* skin type questionnaire. * Subject with sensitive skin as confirmed by Lactic Acid Stinging Test. Exclusion Criteria: * Subject having skin irritation, blemishes, excessive hair, moles, pigmentation, pimples, marks (e.g. tattoos (within the previous 3 months), scars, sunburn), open wounds, cuts, abrasions, irritation symptoms or any dermatological condition on the test site(s) i.e. back that can interfere with the reading. * Medication which may affect skin response and/or past medical history. * Subject having history of diabetes * Subject have history of mastectomy for cancer involving removal of lymph nodes within the past year, or treatment of any type of cancer within the last 6 months. * Subject suffering from any active clinically significant skin diseases which may contraindicate. * Subject having history of any skin diseases including eczema, atopic dermatitis or active cancer. * Participation in any patch test for irritation or sensitization within the last four weeks. * Subject having history of asthma or COPD (Chronic obstructive pulmonary disease). * Use of any: * Prescribed or over-the-counter (OTC) anti-inflammatory drug within five (5) days prior to application. * Antihistamine medication or immunosuppressive drugs within seven (7) days prior to first patch application. iii. Systemic or topical corticosteroids at patch site within four (4) weeks of test product application (steroidal nose drops and/or eye drops are permitted) * Topical drugs used at application site. * Subject with Self-reported Immunological disorders such as HIV positive, AIDS and/or systemic lupus erythematous. * Individual who has a medical condition or is taking or has taken a medication which, in the Investigator's judgment, makes the subject ineligible or places the subject at undue risk. * Subject with known allergy or sensitization to medical adhesives, bandages. * Participation in other patch study simultaneously

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As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Contacts and locations

Locations

  • NovoBliss Research

    Ahmedabad, Gujarat, 382481, India

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