New dermal filler tested for wrinkle reduction
NCT ID NCT07329608
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times
Summary
This study looked at the safety and performance of RefillHA Volume, a dermal filler used to smooth facial wrinkles and add volume. It involved 78 adults who wanted wrinkle correction. Researchers tracked side effects and how well the filler worked in everyday clinic use.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- RefillHA Volume (hyaluronic acid dermal filler)
- What this could lead to
- If results are positive, it could confirm that RefillHA Volume is a safe and effective option for reducing facial wrinkles and folds.
- What could go wrong
- This is a small, completed observational study with no comparison group, so results may not apply to everyone. Side effects like swelling or bruising are possible.
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
-
78 people
The number who actually took part.
- Started
-
Jan 2024
- Finished
-
May 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
Subjects over the age of 18 who are seeking correction of facial wrinkles and folds and/or soft tissue augmentation.
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
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: * Adult men and women, over the age of 18, seeking correction of facial wrinkles and folds and/or soft tissue augmentation. * Subjects who are willing and able to read, understand and sign informed consent. Exclusion Criteria: * Subjects with known contraindications to the treatment (as per device IFU). * Subjects considered to be unsuitable to participate, in the investigator's opinion, for any reason.
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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
-
Glyance Ltd
Lod, 7152026, Israel
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