MAITLAND MOBILIZATION VERSUS THERAPEUTIC ULTRASOUND ON TRISMUS FOLLOWING THIRD MOLAR SURGERY
EFFECT OF MAITLAND MOBILIZATION VERSUS THERAPEUTIC ULTRASOUND ON TRISMUS FOLLOWING THIRD MOLAR SURGERY
1 other identifier
interventional
60
1 country
1
Brief Summary
This study aims to compare the effect of Maitland mobilization and therapeutic ultrasound on trismus (limited mouth opening) following third molar (wisdom tooth) surgery. Participants who experience limited mouth opening after third molar surgery will receive one of two treatment methods: Maitland joint mobilization or therapeutic ultrasound. These treatments are commonly used in physical therapy to improve jaw movement and reduce stiffness. The purpose of this study is to determine which treatment is more effective in improving mouth opening and reducing symptoms after surgery. Participation is voluntary, and all collected information will be kept confidential and used only for research purposes.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Oct 2025
Shorter than P25 for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 10, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 20, 2026
CompletedStudy Completion
Last participant's last visit for all outcomes
March 10, 2026
CompletedFirst Submitted
Initial submission to the registry
May 3, 2026
CompletedFirst Posted
Study publicly available on registry
May 8, 2026
CompletedMay 8, 2026
May 1, 2026
4 months
May 3, 2026
May 3, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Pain intensity level
Pain intensity level via The Visual Analog Scale (VAS): The VAS is self-completed by the participant. The participant is asked to place a line perpendicular to the VAS 100 mm line at the point that represents their pain intensity. The examiner reported the VAS score by measuring the distance (mm) from the marked point to the "no pain" anchor using a ruler, providing a range of scores from 0 -100 (Boonstra et al., 2008)
Baseline, immediately post-intervention
Secondary Outcomes (1)
Maximum Interincisal Opening
Baseline, immediately post-intervention
Study Arms (3)
Maitland Mobilization Group
EXPERIMENTALParticipants in this group received Maitland mobilization techniques applied to the temporomandibular joint. The intervention was performed by a trained therapist using graded passive mobilization techniques aimed at improving joint mobility and reducing trismus. Treatment sessions were conducted over the study period with standardized frequency and duration
Therapeutic Ultrasound group
EXPERIMENTALParticipants received therapeutic ultrasound applied to the temporomandibular joint and surrounding muscles. The ultrasound was delivered at a frequency of 1 MHz to target deep tissues. Treatment sessions were conducted three times per week for four weeks, with each session lasting 10-15 minutes. A water-based conductive gel was applied to enhance transmission of sound waves. The intensity ranged from 0.8 to 1.5 W/cm² based on patient tolerance, and the transducer was moved in slow circular motions over the affected area to reduce pain and stiffness
Control group
ACTIVE COMPARATORtraditional physical therapy program (Standard Postoperative Care, Cold Compresses/Ice Packs, NSAIDs);
Interventions
Maitland mobilization was applied to the temporomandibular joint using graded passive accessory and physiological joint mobilization techniques (Grade I-IV depending on patient tolerance). The technique was performed by a trained physical therapist to improve joint mobility and reduce trismus following third molar surgery. Treatment sessions were conducted three times per week for four weeks
using an ultrasound device , such as the Chattanooga Intelect Mobile 2, which operates at a 1 MHz frequency to target deep tissues like the temporomandibular joint (TMJ) and surrounding muscles. The therapy was conducted three times a week for four weeks, with each session lasting 10-15 minutes. A water-based conductive gel was applied to the skin to facilitate effective transmission of sound waves, and the intensity of the ultrasound was adjusted between 0.8 to 1.5 W/cm² based on patient tolerance. The transducer was moved in slow, circular motions over the TMJ and affected muscles, focusing on areas of pain or stiffness (Bhushan et al., 2025).
the traditional physical therapy program (Standard Postoperative Care, Cold Compresses/Ice acks, NSAIDs);
Eligibility Criteria
You may qualify if:
- Patients were included in this study have the following criteria
- Sixty patients had done third molar extraction surgery
- Patients suffering from postoperative trismus within 2 to 14 days post-surgery.
- Their age between 20 and 30 years old
You may not qualify if:
- The study excluded the following patients:
- Pre-existing TMJ Disorders: Patients with a history of temporomandibular joint (TMJ) disorders or jaw-related conditions (e.g., TMJ dislocation, arthritis, or previous TMJ surgery).
- Neurological or Muscular Disorders: (e.g., facial palsy, stroke, muscular dystrophy).
- Previous Jaw Surgery or Trauma.
- Use of Muscle Relaxants or other form of Physical Therapy treatment.
- Chronic Pain Syndromes: such as fibromyalgia or chronic migraines
- Infections or abscesses post-Surgery.
- Patients have auditory and visual problems
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Cairo Universitylead
Study Sites (1)
Abu Hammad General Hospital
Abū Ḩammād, El-Sharqia Governorate, Egypt
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Masking Details
- This study was conducted as an open-label trial. No masking was applied, and both participants and investigators were aware of the assigned interventions in all study arms
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Physical Therapist (MSc Candidate)
Study Record Dates
First Submitted
May 3, 2026
First Posted
May 8, 2026
Study Start
October 10, 2025
Primary Completion
February 20, 2026
Study Completion
March 10, 2026
Last Updated
May 8, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share