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
| Type | Name | Description |
|---|---|---|
| DRUG | Botulinum toxin type A | Single 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.