Actively Recruiting
Treatment of Chronic Temporomandibular Pain With Peripheral Nerve Block
Led by Bnai Zion Medical Center · Updated on 2025-06-10
40
Participants Needed
1
Research Sites
8 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This research aims to evaluate the use of peripheral nerve blocks for treating chronic jaw pain caused by temporomandibular disorders (TMD). It focuses on adults who have had jaw pain for over a year and have not found relief from at least two other treatments like physical therapy or medication. The study is conducted at a TMJ clinic and seeks to collect structured data on pain and function after the nerve block treatment. The treatment involves injecting anesthetic near specific nerves around the jaw joint to block pain signals. This procedure is part of the patients' regular clinical care at the TMJ clinic. Participants receive the nerve block and then attend follow-up visits, typically every four months, to monitor their progress. The study plans to include up to 40 adults and will observe their response to this treatment over time. Participants will be monitored through regular visits where researchers assess pain levels using a pain scale, measure mouth opening ability, and track changes in pain medication use. Follow-up visits are usually scheduled three times per year, with additional visits if symptoms worsen. Participants must attend at least two follow-ups to stay in the study and can leave at any time without affecting their care. Personal information is securely stored and coded to protect privacy throughout the study period.
CONDITIONS
Brief Title
Nerve Block Treatment for Chronic Jaw Pain
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults who are mentally competent and not pregnant
- Chronic temporomandibular joint pain lasting at least 12 months
- Have tried and not responded to at least two previous treatment methods
You will not qualify if you...
- Not meeting the inclusion criteria
- Missing at least two follow-up visits within the specified timeframe
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person)
Duration - Single treatment event
Participants receive a peripheral nerve block as part of their routine clinical care for chronic temporomandibular pain.
1 treatment visit (in-person)
Duration - Up to 12 months
Participants are observed with follow-up visits to assess pain levels, mouth opening, medication use, and need for repeat treatments.
Approximately 3 follow-up visits per year, typically every 4 months with additional visits if symptoms worsen
Trial Site Locations
Total: 1 location
1
Department of Oral and Maxillofacial Surgery
Haifa, North, Israel, 3199500
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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