CTRI/2020/06/025824
Active, Not Recruiting
Phase 4
Efficacy of a novel vibrator device in comparision to ultrasonic device for the management of myofascial pain dysfunction syndrome- a randomized clinical trial
Govt Dental College0 sites52 target enrollmentTBD
Overview
- Phase
- Phase 4
- Intervention
- Not specified
- Conditions
- Health Condition 1: M958- Other specified acquired deformities of musculoskeletal system
- Sponsor
- Govt Dental College
- Enrollment
- 52
- Status
- Active, Not Recruiting
- Last Updated
- 3 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\.Patients who are willing to participate
- •2\.Patients who have experienced chronic and intermittent myofascial pain for a time period of 1 month or more
- •3\.Patients meeting Laskinââ?¬•s criteria for MPDS
Exclusion Criteria
- •1\.History of recent trauma
- •2\.Patients who are receiving any medication or treatment other than vibration therapy and ultrasound therapy
- •3\.Patients with gross malocclusion
- •4\.History of TMJ pathology such as internal derangement or disc pathology and any invasive procedure on TMJ
- •5\.Patients with uncontrolled Diabetes Mellitus
- •6\.Neurological disorders such as trigeminal neuralgia
- •7\.Any previous history of adverse reaction to vibration therapy
Outcomes
Primary Outcomes
Not specified
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