Clinical Trials Directory

Trials / Completed

CompletedNCT05309564

Muscle Weakness Duration After Single Botulinum Toxin Injection in Masseter

Muscle Weakness Duration Post-injection of a Single Dose of Botulinum Toxin in the Masseter Muscle Bilaterally: a One-year Non-randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
32 (actual)
Sponsor
Region Västerbotten · Other Government
Sex
Female
Age
18 Years – 120 Years
Healthy volunteers
Accepted

Summary

This study aimed to evaluate the duration of a reduced maximal voluntary bite force after a botulinum toxin intervention. Methods: In an intervention group, 25 units of Xeomin® (Merz Pharma GmbH \& Co KGaA, Frankfurt am Main, Germany) botulinum neurotoxin type A were injected into the masseter muscles bilaterally (to a total of 50 units).

Detailed description

This study aimed to evaluate the duration of a reduced maximal voluntary bite force (MVBF) after a botulinum toxin intervention. Methods: In an intervention group, 25 units of Xeomin® (Merz Pharma GmbH \& Co KGaA, Frankfurt am Main, Germany) botulinum neurotoxin type A were injected into the masseter muscles bilaterally (to a total of 50 units). A control group did not receive any intervention. MVBF was measured in Newtons using a strain gauge meter at the incisors and first molars. The intervention group was comprised of individuals seeking aesthetic treatment for masseter reduction (n = 20), and the control group (n = 12) comprised of volunteers.

Conditions

Interventions

TypeNameDescription
DRUGBotulinum toxin type ASingle intervention

Timeline

Start date
2020-03-01
Primary completion
2022-01-10
Completion
2022-03-14
First posted
2022-04-04
Last updated
2023-05-03

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT05309564. Inclusion in this directory is not an endorsement.