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Clinical trialNCT03048383CompletedPhase 4Interventional

Comparison of Three Botulinum Neuromodulators for Management of Facial Synkinesis

SponsorUniversity of UtahEnrollment71Facial AsymmetryFacial Nerve InjuriesFacial Paresis Associated With Facial Nerve DysfunctionSynkinesis
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

The purpose of this study is to compare the effectiveness of three commercially available botulinum toxin neuromodulators in the treatment of facial synkinesis using patient reported outcome measures.
clinicaltrials.gov ↗

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

No facility list is in our current data snapshot for this study. The registry record on ClinicalTrials.gov ↗ carries any published locations. Why? →

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

AbobotulinumtoxinA Injectable ProductIncobotulinumtoxin A Injectable ProductOnabotulinumtoxinA Injectable Product
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
31 Jul 2012
Primary completion
31 Mar 2015
Completion
31 Mar 2015
Last update posted
31 Jul 2017
Registered enrollment
71
Registry id
NCT03048383
clinicaltrials.gov ↗

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.