Trial Review

The ANZCTR website will be unavailable from 1pm until 3pm (AEDT) on Wednesday the 30th of October for website maintenance. Please be sure to log out of the system in order to avoid any loss of data.

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been endorsed by the ANZCTR. Before participating in a study, talk to your health care provider and refer to this information for consumers
Trial registered on ANZCTR


Registration number
ACTRN12618001430224
Ethics application status
Approved
Date submitted
19/12/2017
Date registered
27/08/2018
Date last updated
23/03/2023
Date data sharing statement initially provided
30/11/2021
Date results provided
23/03/2023
Type of registration
Retrospectively registered

Titles & IDs
Public title
Botulinum toxin for nocturnal bruxism.
Scientific title
Efficacy of Botulinum Toxin Type A in the Targeted Treatment of Nocturnal Bruxism: A Double-Blind, Randomised, Placebo-Controlled Cross-over Study
Secondary ID [1] 293593 0
None
Universal Trial Number (UTN)
Trial acronym
Linked study record

Health condition
Health condition(s) or problem(s) studied:
Bruxism 305847 0
Condition category
Condition code
Neurological 305056 305056 0 0
Other neurological disorders
Oral and Gastrointestinal 305057 305057 0 0
Other diseases of the mouth, teeth, oesophagus, digestive system including liver and colon

Intervention/exposure
Study type
Interventional
Description of intervention(s) / exposure
The intervention is a set of injections at 2 time points, at least 20 weeks apart, performed by a trained neurologist at Royal Melbourne Hospital. The treatment consists of intramuscular injections of Botox (onabotulinumtoxinA) (dose range of 90-120units as detailed below) and 0.9% normal saline (dose range 1.8ml-2.4ml), in a randomised, double blind, cross-over study.

The doses detailed are based on the minimally clinically effective doses within the range of those used in published studies.

Patients will be randomised to receive injections into:
A. Masseter muscles bilaterally (30 units or 0.6ml normal saline each side);
B. Masseter and temporalis muscles bilaterally (30 units/15 units each muscle respectively, or 0.6ml/0.3ml respectively); or
C. Masseter, temporalis and medial pterygoid muscles bilaterally (30units/15units/15 units each muscle respectively, or 0.6ml/0.3ml/0.3ml normal saline respectively).

The duration of treatment effect for botulinum toxin injected into the face, head and neck area has been observed to be approximately 3-4 months. Therefore a 20-week (5month) washout period was chosen to ensure that there is no remaining active treatment effect before the cross-over set of injections.

At 20 weeks, there will therefore be a single set of injections, of either active treatment or placebo, in the same sites as the first injection, again performed by a trained Neurologist at Royal Melbourne Hospital.

Study investigators will contact the participants to arrange followup within 7 days of the specified timepoint, for clinical assessment and outcome measures. Participants will also be given dates for followup in advance of the scheduled timepoints to ensure fidelity to the intervention followup schedule.
Intervention code [1] 299847 0
Treatment: Drugs
Comparator / control treatment
Placebo (0.9% normal saline, 1.8-2.4ml)
Control group
Placebo

Outcomes
Primary outcome [1] 304222 0
Composite primary outcome: change in bruxism severity (objectively measured by overnight surface EMG, validated questionaires addressing bruxism (Bruxism symptom questionnaire), headache (headache impact test (HIT-6) questionnaire, pain (modified Short-Form McGill pain scale) and sleepiness severity (using the Epworth sleepiness scale), following injection of onabotulinum toxin and placebo.
Timepoint [1] 304222 0
4 weeks following injection of onabotulinum toxin or placebo.
Primary outcome [2] 304223 0
Safety of botulinum toxin in the treatment of nocturnal bruxism as measured by clinical review. A neurologist will be clinically assessing the participant, discussing any change in health or possible side-effects of the treatment and documenting details.

The possible expected side effects are bruising/discomfort and rarely excessive muscle weakness (manifest as weakness with chewing).
Timepoint [2] 304223 0
4 weeks following injection of onabotulinum toxin or placebo
Secondary outcome [1] 351141 0
Duration of benefit following Botulinum toxin injection on symptoms of Bruxism.
Timepoint [1] 351141 0
Weeks 4, 12, 20 following injection of either placebo or Botulinum toxin

Eligibility
Key inclusion criteria
Symptoms of nocturnal bruxism of adequate severity as measured by overnight monitoring.
Minimum age
18 Years
Maximum age
No limit
Sex
Both males and females
Can healthy volunteers participate?
No
Key exclusion criteria
Contraindication to botulinum toxin administration, concurrent use of medications affecting muscle relaxation, prior history of severe jaw trauma, orofacial pain of an alternate aetiology, neuromuscular disease, major respiratory disease(s) that may preclude overnight EMG recordings, administration of botulinum toxin for other indication (including cosmetic) within 16weeks of study commencement.

Study design
Purpose of the study
Treatment
Allocation to intervention
Randomised controlled trial
Procedure for enrolling a subject and allocating the treatment (allocation concealment procedures)
Methods used to generate the sequence in which subjects will be randomised (sequence generation)
Masking / blinding
Blinded (masking used)
Who is / are masked / blinded?
The people receiving the treatment/s
The people administering the treatment/s
The people assessing the outcomes
The people analysing the results/data
Intervention assignment
Crossover
Other design features
Phase
Phase 2
Type of endpoint/s
Safety/efficacy
Statistical methods / analysis

Recruitment
Recruitment status
Completed
Date of first participant enrolment
Anticipated
Actual
5/02/2016
Date of last participant enrolment
Anticipated
Actual
29/11/2019
Date of last data collection
Anticipated
Actual
5/10/2020
Sample size
Target
30
Accrual to date
Final
41
Recruitment in Australia
Recruitment state(s)
VIC
Recruitment hospital [1] 9542 0
Royal Melbourne Hospital - City campus - Parkville
Recruitment postcode(s) [1] 18296 0
3050 - Parkville

Funding & Sponsors
Funding source category [1] 298210 0
Hospital
Name [1] 298210 0
Melbourne Health
Country [1] 298210 0
Australia
Primary sponsor type
Hospital
Name
Melbourne Health
Address
Royal Melbourne Hospital
Grattan Street,
Parkville, VIC 3050
Country
Australia
Secondary sponsor category [1] 297313 0
None
Name [1] 297313 0
N/A
Address [1] 297313 0
N/A
Country [1] 297313 0

Ethics approval
Ethics application status
Approved
Ethics committee name [1] 299217 0
Melbourne Health Human Research Ethics Committee
Ethics committee address [1] 299217 0
Ethics committee country [1] 299217 0
Australia
Date submitted for ethics approval [1] 299217 0
26/08/2015
Approval date [1] 299217 0
01/12/2015
Ethics approval number [1] 299217 0
2015.195

Summary
Brief summary
Trial website
Trial related presentations / publications
Public notes

Contacts
Principal investigator
Name 79694 0
A/Prof Lynette Kiers
Address 79694 0
4N Neurophysiology
Royal Melbourne Hospital
Grattan Street
Parkville
VIC 3050
Country 79694 0
Australia
Phone 79694 0
+61 03 93427693
Fax 79694 0
+61 03 93424085
Email 79694 0
[email protected]
Contact person for public queries
Name 79695 0
Belinda Cruse
Address 79695 0
4N Neurophysiology
Royal Melbourne Hospital
Grattan Street
Parkville
VIC 3050
Country 79695 0
Australia
Phone 79695 0
+61 03 93427693
Fax 79695 0
+61 03 93424085
Email 79695 0
[email protected]
Contact person for scientific queries
Name 79696 0
Belinda Cruse
Address 79696 0
4N Neurophysiology
Royal Melbourne Hospital
Grattan Street
Parkville
VIC 3050
Country 79696 0
Australia
Phone 79696 0
+61 03 93427693
Fax 79696 0
+61 03 93424085
Email 79696 0
[email protected]

Data sharing statement
Will individual participant data (IPD) for this trial be available (including data dictionaries)?
No
No/undecided IPD sharing reason/comment


What supporting documents are/will be available?

No Supporting Document Provided



Results publications and other study-related documents

Documents added manually
No documents have been uploaded by study researchers.

Documents added automatically
SourceTitleYear of PublicationDOI
EmbaseEfficacy of botulinum toxin type a in the targeted treatment of sleep bruxism: a double-blind, randomised, placebo-controlled, cross-over study.2022https://dx.doi.org/10.1136/bmjno-2022-000328
N.B. These documents automatically identified may not have been verified by the study sponsor.