Head-to-Head Comparison of All Botulinum Neurotoxin Type A Products for Glabellar Rhytides

Recruiting Phase 4 Interventional Study
Wrinkle Glabellar Frown Lines Glabellar Furrowing
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 and older
Sex
Female
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
325 (estimated)
Sponsor
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA) · Other
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About This Trial
Study Type: This is a multicenter, triple-blind, randomized controlled trial. Purpose: The goal of this clinical trial is to compare the effectiveness and safety of all commercially available Botulinum Neurotoxin Type A (BoNT-A) products for treating glabellar rhytides, commonly known as frown lines. This study is designed to provide comprehensive data on how these treatments compare in terms of …
Trial Locations
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Eligibility Criteria
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…
Contacts

Serge A. Steenen, MD DMD

+316 26 457 415

s.a.steenen@amsterdamumc.nl

CONTACT