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Efficacy of Botulinum Toxin A in the Treatment of Bruxism-related Symptomatology

Efficacy of Botulinum Toxin A in the Treatment of Bruxism-related Symptomatology

Status
Terminated
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04722809
Acronym
Botox
Enrollment
1
Registered
2021-01-25
Start date
2022-05-25
Completion date
2022-08-31
Last updated
2024-08-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bruxism

Brief summary

Bruxism is defined as a parafunction that consists of a clenching of the jaw and/or grinding of the teeth. It can occur when an individual is sleeping or awake or it can be mixed. Most often, it is primary or idiopathic bruxism, however when it is related to a cause it is qualified as secondary. Primary bruxism is a condition that is not well known to the general public, but I is very widespread (12% of the adult population). In addition, it can alter quality of life, as a result of associated sleep disorders, concentration disorders, daytime fatigue, chronic pain, etc. The current treatment for this condition is only symptomatic. Currently, one of the most effective treatments is the intramuscular injection of botulinum toxin A in the muscles of mastication. The progressive anticholinergic action results in a reduction of functional signs (dental pain, periodontal pain, temporomandibular joint pain, tension headaches, neck pain) and physical signs (reduction of the mass of the injected muscles, alba linea, tongue scalloping, limitation or stability of dental damage). However, these clinical data are practically not objectified in daily practice. Objective criteria would make it possible to measure the effectiveness of the treatment, to follow the patient, and to identify the early symptoms in order to prevent a recurrence. The aim of the prospective study is to concretely measure the strength and electromyographic activity of the muscles of mastication before and after botulinum toxin injection.

Interventions

Injection in the temporal and masseter muscles: in 3 points in the masseter muscles and in 2 points in the temporal muscles.

OTHERQOL-Brux

Questionnaire evaluating the symptoms of bruxism Inclusion and 3 months post-injection

OTHERMuscular strength of the jaw

Measurement in the jaw with a dynamometer connected to a sensor placed on the 1st molar on the right side. At inclusion and 1 month post-injection.

OTHERIntensity and frequency of episodes of nocturnal bruxism

Measurements via a portable electromyography system, coupled with a heartbeat sensor (Bruxoff®). Measurements performed during normal sleeping conditions at home before injection and 1 month after.

OTHERvisual analogue pain scale

Evaluation of jaw pain. At inclusion and 3 months post-injection

OTHEREndobuccal and linea alba photographs

anonymous endobuccal and linea alba photographs (line on the inner face of the cheeks as the result of chronic friction). At inclusion

Sponsors

Centre Hospitalier Universitaire Dijon
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 64 Years
Healthy volunteers
No

Inclusion criteria

* Patient who has given written consent. * Patient between 18 and 64 years of age. * Patient who has never received botulinum toxins * Symptomatic patient in the context of bruxism in failure to the usual treatments (analgesic, physiotherapy, relaxation technique and maxillary retainer) * Woman of childbearing age using an effective method of contraception * Symptomatic patients in the context of bruxism, without a maxillary disocclusion retainer.

Exclusion criteria

* Protected Adult * Patient not affiliated to the national health insurance system * Pregnant or breastfeeding woman * Refusal to take part in the study * Neuromuscular diseases, including Myasthenia gravis, Myopathies, Amyotrophic Lateral Sclerosis. Lambert-Eaton Syndrome, patients with peripheral motor neuropathies, patients with underlying neurological disorders. * Patients with a history of cardiovascular disease * Patients with epilepsy or a previous seizure episode * Neurogenic impairment of the face (including facial paralysis, polyradiculoneuritis) * History of dysphagia or pulmonary aspiration * Injection site infection (masseter and temporal) * Hypersensitivity or allergy to botulinum toxin or any of its excipients. * Treatment with aminoglycosides or anticholinesterase agents.

Design outcomes

Primary

MeasureTime frameDescription
number of episodes of nocturnal bruxism1 month after treatment by botulinum toxin injectionmeasurement of the number of bruxism episodes via a portable electromyogram we expect a significant improvement in the number of nocturnal bruxism episodes (decrease in relation to time 0)

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026