Diacutaneus Fibrolysis on Tempromandibular Joint Pain and Trismus Post Oral Surgery
Not Applicable
Active, not recruiting
- Conditions
- TMJ Pain
- Registration Number
- NCT06675149
- Lead Sponsor
- Cairo University
- Brief Summary
This study is carried out on sixty patients who will have tempromandibular pain and trismuspostOral and Maxillofacial Surgeryand their ages will be ranged from 18 to 40 years.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ACTIVE_NOT_RECRUITING
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
- Ages of patients will be ranged from 18 to 40 years.
- All patients will have Oral and Maxillofacial Surgery.
- All patients will be referred by a surgeon before starting the study procedure.
- All participants will have pain and trismus in the jaw,
- The participants will be also cleared for periodontal issues.
- All patients will enter the study having their informed consent
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Exclusion Criteria
- Patients with associated vascular injuries requiring arterial repair.
- Patient with systemic diseases such as arthritis; pain attributable to confirmed migraine, head, or neck pain condition
- Patient with acute infection or other significant disease of the teeth, ears, eyes, nose, or throat
- Patient with present neurologic or cognitive deficit.
- Patients with history of previously failed surgeries.
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Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Primary Outcome Measures
Name Time Method temporomandibular joint pain pre intervention and re assessed after 1 month pain is assessed Pressure pain threshold(PPT) will be obtained with the aid of an algometer by applying pressure to the masseter and to the anterior, middle, and posterior temporalis, increasing pressure until the patient will feel that the pressure will become unpleasant or "painful .
Trismus pre intervention and re assessed after 1 month Trismus is assessed by caliper
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Cairo University
🇪🇬Giza, Egypt