Temporomandibular Joint Disorders, Articular Disc Disorder (Reducing or Non-Reducing)
Conditions
Keywords
Temporomandibular Joint Disorders
Brief summary
The present study will be designed to compare the short- and medium-term results of arthrocentesis and non-surgical methods Rocabado approach in early disc displacement without reduction.
Detailed description
This study will be designed to provide a comparison between the effect of the Rocabado approach as a conservative treatment and temporomandibular joint arthrocentesis in temporomandibular joint disc displacement without reduction. Delimitations: This study will be delimited in the following aspects: 1. Patients: The study group will be composed of sixty-eight patients with temporomandibular joint disc displacement without reduction will be enrolled in the study. Group A: It will be composed of thirty-four patients with TMJ disc displacement without reduction who are started on the Rocabado approach- 4 - 6×6 exercise program. Include therapeutic exercise, and patient education focusing on the temporomandibular joint. Repeat measurements will be performed on 1st measurement at the baseline before any intervention, 2nd measurement after 8 weeks of treatment by a physiotherapist. Group B: It will be composed of thirty-four patients with disc displacement without reduction who are started on TMJ arthrocentesis procedure with medical and nursing care. 2. Equipment and tools: 2.1-Measurement equipment: Thera bite ROM scale 8-Item Jaw Functional Limitation Scale (JFLS-8) (Valid Arabic version) visual anlogue scale 2.2-Therapeutic procedures: Rocabado's 6X6 Exercise Program and manibulation
Interventions
Rocabado's approach (Rocabado's 6 × 6 Exercises and manipulation). This program included 6 exercises to be performed 6 times a day, repeated 6 times, and three gliding exercises.
Participants in the Control Group underwent arthrocentesis of the affected temporomandibular joint. The procedure was performed as follows: Anesthesia: Local anesthesia was administered to the area surrounding the TMJ. Needle Insertion: A 20-gauge needle was inserted into the upper joint space approximately 10 mm anterior to the tragus. Lavage: The joint was lavaged with lactated Ringer's solution to reduce inflammation and remove debris. The joint was irrigated with lactated Ringer's solution.
Sponsors
Study design
Eligibility
Inclusion criteria
* History of a sudden reduction in the mandibular opening. Unassisted mandibular opening 35 mm. * Mandibular opening with assistance increased by ≥3 mm from * unassisted opening, with a prior history of click, click disappearance, and a sudden decrease in opening. * Magnetic resonance imaging (MRI) diagnosis of Disc displacement without reduction. * Persistence of the symptoms indicated in the first item for a Maximum of 3 weeks. * clinical diagnosis of unilateral Disc displacement without reduction of the temporomandibular joint.
Exclusion criteria
* History of major jaw trauma. * Dentofacial deformity. * Psychiatric illness. * Chronic headache. Presence of other disorders involving the TMJ.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Thera Bite RANGE OF MOTION scale | pre treatment and eight weeks post treatment | Will be used for measuring the Maximal interincisal opening, lateral movement will be measured. Measuring Maximal Interincisal Opening : 1. Patient Positioning: The patient opens their mouth as wide as possible without discomfort. 2. Scale Placement: The range of motion scale is positioned so that the notch rests on the edge of the lower incisor. 3. Measurement: Rotate the scale until it contacts the upper incisor, and record the reading at the point of contact. Measuring Lateral Excursion Movement: 1. Scale Alignment: Rest the range of motion scale against the lower incisors with the upper and lower teeth closed together. 2. Arrow Alignment: Align the arrow on the scale with an interproximal space between two upper teeth. 3. Measurement: Move the mandible laterally (side-to-side) and record the measurements on the lateral side. |
| 8-Items Jaw Functional Limitation Scale | pre treatment and eight weeks post treatment | Disability related to orofacial pain, which makes it a generic tool that one can use it for different types of orofacial pain conditions. 1. Preparation: Select a quiet and distraction-free environment. 2. Understanding the Scale: Rate each item on a scale from 0 (no limitation) to 10 (severe limitation). 3. Completing the Questionnaire: Carefully read each question and reflect on your jaw function over the past week. 4. Items to Rate: Assess difficulties in chewing, mouth opening, and emotional expression. 5. Time Required: Completion typically takes less than 5 minutes. 6. Post-Completion: Higher scores indicate greater functional limitations. |
| Visual analog scale | pre treatment and eight weeks post treatment | One of the pain rating scales, 1. Preparation: Ensure the VISUAL ANALOG SCALE line is accurately printed to scale (10 cm) with endpoints labeled: * 0 = No pain. * 10 = Worst imaginable pain. 2. Patient Instructions: Ask the patient to mark their current pain level on the line. 3. Score Measurement and Interpretation: Measure the distance in centimeters from the no pain end (0) to the patient's mark to determine the score out of 10. Higher scores indicate greater pain intensity (e.g., a mark at 6 cm corresponds to a pain level of 6/10). 4. Recall Period: Patients report either their current pain or pain experienced within the last 24 hours, depending on assessment context. |
Countries
Egypt