About this trial
Both patients and remitters ask for treatment with Botulinumtoxin A (BTX) with the hope that it will be an effective aid for pain, but little is known regarding if the effect is dose dependent.
The aim of this project is to investigate if injections with BTX in the masseter- and temporal muscle is an efficient treatment in patient with myogenous temporomandibular disorders (TMD) and if the effect of BTX is dose dependent.
Eligibility criteria
Qualifiers
Has given a written consent
Diagnose of myalgia, myofacial pain or myofascial pain with referred pain according
Average pain due to NRS ≥ 3 for more than three months
Palpationpain in masseter or temporalis.
Disqualifiers
Treatment with BTX during the last 12 months
Treatment for orofacial pain within the last 3 months.
Systemic inflammatory diseases (rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis)
Widespread pain e.g., fibromyalgia
Trial design
Treatments tested in this trial
- 5U/0,1 ml Botulinum toxin A
- 10U/0,1 ml Botulinum toxin A