NCT07575100

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

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
60

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Oct 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

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

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 20, 2026

Completed
18 days until next milestone

Study Completion

Last participant's last visit for all outcomes

March 10, 2026

Completed
2 months until next milestone

First Submitted

Initial submission to the registry

May 3, 2026

Completed
5 days until next milestone

First Posted

Study publicly available on registry

May 8, 2026

Completed
Last Updated

May 8, 2026

Status Verified

May 1, 2026

Enrollment Period

4 months

First QC Date

May 3, 2026

Last Update Submit

May 3, 2026

Conditions

Keywords

Maitland technique, Ultrasound, maximum mouth opening, trismus, third molar surgery.

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

EXPERIMENTAL

Participants 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

Procedure: Maitland Joint Mobilization

Therapeutic Ultrasound group

EXPERIMENTAL

Participants 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

Device: Therapeutic Ultrasound group

Control group

ACTIVE COMPARATOR

traditional physical therapy program (Standard Postoperative Care, Cold Compresses/Ice Packs, NSAIDs);

Other: Control group

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

Maitland Mobilization Group

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).

Therapeutic Ultrasound group

the traditional physical therapy program (Standard Postoperative Care, Cold Compresses/Ice acks, NSAIDs);

Control group

Eligibility Criteria

Age20 Years - 30 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

Study Sites (1)

Abu Hammad General Hospital

Abū Ḩammād, El-Sharqia Governorate, Egypt

Location

MeSH Terms

Conditions

Trismus

Interventions

Control Groups

Condition Hierarchy (Ancestors)

SpasmNeuromuscular ManifestationsNeurologic ManifestationsNervous System DiseasesSigns and SymptomsPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Epidemiologic Research DesignEpidemiologic MethodsInvestigative TechniquesResearch DesignMethods

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
Model Details: This study used a parallel assignment design. Participants diagnosed with trismus following third molar surgery were randomly allocated into three independent groups: Maitland mobilization group, therapeutic ultrasound group, and a control group. Each intervention group received its assigned treatment separately during the study period
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

Locations