New gel for Women's dryness passes safety test in small study
NCT ID NCT07533461
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested a product called GINHI on 20 healthy women aged 18-65 to see if it is safe and pleasant for daily use. The women applied the product twice a day and answered questions about dryness, itching, and how the product felt. The goal was to confirm the product is acceptable for the skin and does not cause unwanted reactions.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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20 people
The number who actually took part.
- Started
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Jun 2024
- Finished
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Jul 2024
- Lead sponsor
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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.
- Ages
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18 to 65 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide 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: * Healthy women * Age between 18 and 65 years * Volunteers with sensitive skin (50%) and normal skin (50%) * Volunteers with Fitzpatrick skin photo-type I to IV * Frequent users of similar product * Adequate cultural level and understanding of the clinical study * To agree to participate voluntarily in the study and grant written Informed Consent. Exclusion Criteria: * Volunteers with chronic or acute disease at study initiation or in the last 3 weeks prior to inclusion * Volunteers with skin pathologies in the last 3 weeks prior to study initiation. * Volunteers under pharmacological treatment. * Pregnant or breast-feeding women. * Volunteers with allergy to any of the study product components. * Vaccinated in the last 3 weeks previous to study start.
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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
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Anmar Clinical Services, S.L.U.
Pamplona, Navarre, 31003, Spain
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