Effect of Diacutaneus Fibrolysis on Tempromandibular Joint Pain and Trismus Post Oral and Maxillofacial Surgery
Trial Snapshot
- Phase
- Not Applicable
- Status
- Completed
- Sponsor
- Cairo University
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- temporomandibular joint pain
Study Overview
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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Treatment
- Masking
- None
Eligibility Criteria
- Ages
- 18 Years to 40 Years (Adult)
- Sex
- All
- Accepts Healthy Volunteers
- No
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
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.
Arms & Interventions
Group B
This group includes 30 patients who will receive 4 weeks(3times/week) DiacutaneusFibrolysis in addition to post-surgical traditional physiotherapy .
Intervention: Diacutaneus fibrolysis (Device)
Group B
This group includes 30 patients who will receive 4 weeks(3times/week) DiacutaneusFibrolysis in addition to post-surgical traditional physiotherapy .
Intervention: Transcutaneous electrical nerve stimulation (Device)
Group B
This group includes 30 patients who will receive 4 weeks(3times/week) DiacutaneusFibrolysis in addition to post-surgical traditional physiotherapy .
Intervention: Massage (Procedure)
Group A
This group will includes 30 patients who will receive 4 weeks (3times/week) post-surgical traditional physiotherapy (TENS , massage , range of motion exercise ) .
Intervention: Transcutaneous electrical nerve stimulation (Device)
Group A
This group will includes 30 patients who will receive 4 weeks (3times/week) post-surgical traditional physiotherapy (TENS , massage , range of motion exercise ) .
Intervention: Massage (Procedure)
Outcomes
Primary Outcomes
temporomandibular joint pain
Time Frame: 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
Time Frame: pre intervention and re assessed after 1 month
Trismus is assessed by caliper
Secondary Outcomes
No secondary outcomes reported
Investigators
Aliaa Elsayed Ali
Demonstrator
Cairo University