CompletedNot Applicable

MAITLAND MOBILIZATION VERSUS THERAPEUTIC ULTRASOUND ON TRISMUS FOLLOWING THIRD MOLAR SURGERY

Egypt60 participantsStarted 2025-10-10

Plain-language 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.

Who can participate

Age range20 Years – 30 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * 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 * All patients are medically and clinically stable when attending the study 2.1.2. Exclusion criteria: 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

What they're measuring

Pain intensity level

Timeframe: Baseline, immediately post-intervention

Trial details

NCT IDNCT07575100

SponsorCairo University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2026-02-20