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Scientists map skin microbiome shifts across decades

NCT ID NCT07431203

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This completed study looked at how the community of bacteria living on your skin (the microbiome) changes as you age. Researchers studied 100 healthy women split into two age groups (25-35 and 55-65) to see if skin microbes relate to biological age and facial features. The goal was simply to observe and understand these connections, not to test a treatment.

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.

Participants

100 people

The number who actually took part.

Started

Oct 2025

Finished

Dec 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Who is studied

The population to be studied will be women between 25 to 35 years old and between 55 to 65 years old in order to evaluate the relationship between skin collection and saliva sampling and skin measurements.

Ages

25 to 65 years

Sex

Female participants only

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: 1. Healthy subject; 2. Sex: female 3. Age: 50% having between 25 to 35 years old or 50% between 55 to 65 years old 4. Type: Caucasian 5. Phototype: I to III on the Fitzpatrick scale 6. Subject, having given freely and expressly her informed consent. 7. Subject, psychologically able to understand the study related information and to give a written informed consent; 8. Subject able to comply with protocol requirements; 9. Female of childbearing potential should use a medically accepted contraceptive regimen since at least 12 weeks before the beginning of the study and during all the study. 10. Women between 55 to 65 years old should be menopausal (last menstrual period at least 12 months before the screening visit Exclusion Criteria: 1. Pregnant or nursing woman or planning a pregnancy during the study; 2. Subject who had been deprived of their freedom by administrative or legal decision or who is under guardianship; 3. Subject who is under guardianship or who is not able to express her consent; 4. Subject in a social or sanitary establishment; 5. Subject suspected to be non-compliant according to the investigator's judgment; 6. Subject having received 6000 euros indemnities for participation in a clinical research in the 12 previous months, including participation in the present study; 7. Subject enrolled in another clinical trial or which exclusion period is not over. 8. Subject with a condition or receiving a medication which, in the investigator's judgment, put the subject at undue risk or which may interfere with the evaluation; 9. Subject suffering from a severe or progressive disease. 10. Subject with current cutaneous inflammatory or infectious processes (eg, acne, herpes), abscess, an unhealed wound, or a cancerous or precancerous lesion on the face that could interfere with the evaluation. 11. Subject with a tattoo, a scar, moles, acne, too many hairs or anything on the studied zones which might interfere with the evaluation. 12. Subject having received injection on the face with botulinum toxin in the year before the screening. 13. Subject having received injection of filling product on the face in the year before the screening visit. 14. Subject having received injection of mesotherapy in the face in the past 6 months before the screening visit. 15. Subject having done a superficial or medium peeling or a superficial scrub on the face within the 2 previous months. 16. Subject having received tensor threads on the face in the two years before the screening visit. 17. Subject having received treatment with a laser, ultrasound or radiofrequency treatment, a dermabrasion, a surgery, a chemical peeling or any other procedure based on active dermal response on the face within the past 6 months. 18. Subject having used LED mask in the three weeks before screening visit 19. Subject undergoing a topical treatment on the face or a systemic treatment: * anti-inflammatory medication and/or anti-histamines during the previous 2 weeks and during the study; * corticosteroids during the 2 previous weeks and during the study; * retinoids, anti-acne treatment and/or immunosuppressors during the 3 previous months and during the study; * any medication stabilized for less than one month. 20. Subject having started or changed her oral contraceptive treatment during the three previous months. 21. Subject under oral hormonal substitutive treatment during the year previous the screening visit 22. Intensive exposure to sunlight or UV-rays within the previous month and/or foreseen during the study; 23. Subject having changed her life habits within the previous month and/or during the study; 24. Subject with an excessive consumption of alcohol (more than 2 glasses of wine per day) and/or tobacco (more than 10 cigarettes per day). 25. Subject having started or changed her face care products and or make-up within the previous month

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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

  • Dermscan

    Villeurbanne, France

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