Which wrinkle treatment lasts longest? Head-to-Head trial of all five botox products
NCT ID NCT06448676
First seen Jul 02, 2026 · Last updated Aug 14, 2026 · Updated 1 time
Summary
This trial compares the effectiveness and safety of all five commercially available botulinum toxin type A products for treating frown lines in women aged 18 and older. Participants receive injections into facial muscles and take weekly smartphone photos to track changes. The goal is to determine which product works best and how long the effects last.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- botulinum toxin type A
- What this could lead to
- If this trial succeeds, it could help doctors choose which botulinum toxin product works best and lasts longest for frown lines.
- What could go wrong
- This is a phase 4 trial comparing existing products, so no new treatment is being discovered. Results may not apply to men or other uses of botulinum toxin.
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
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 325 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- 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: * Women aged 18 years or over, with moderate to severe glabellar lines * Willing to provide written informed consent * American Society of Anesthesiologists (ASA) Physical Status Classification 1 or 2 * Negative pregnancy test Exclusion Criteria: * ASA Classification 3 or over * History of hypersensitivity or adverse reactions to botulinum toxin or any of its components * Infection at the injection site * Previous treatment with botulinum toxin (lifetime) * Pregnant or breastfeeding women * Neuromuscular disorders or conditions that could interfere with the study assessments
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
3 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Faceland
RECRUITINGAmsterdam, Netherlands
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Faceland
RECRUITINGEindhoven, Netherlands
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Faceland
RECRUITINGUtrecht, Netherlands
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Nuceiva safety checked in 756 patients for frown lines