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Ultrasound Versus Virtual Reality on Temporomandibular Disorder

Ultrasound Versus Virtual Reality on Temporomandibular Disorder Following Surgical Tooth Extraction

Status
Not yet recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07575633
Enrollment
50
Registered
2026-05-08
Start date
2026-05-04
Completion date
2026-07-30
Last updated
2026-05-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Temporomandibular Disorders (TMD)

Keywords

Temporomandibular disorder, Ultrasound, Virtual Reality, surgery

Brief summary

The Purpose of the study is to compare between the therapeutic efficacy of ultrasound and VR in decreasing pain and improving ROM for Patients with temporomandibular joint disorder after tooth extraction surgery.

Detailed description

The study will be carried out on patients suffering from temporomandibular joint disorder following tooth extraction surgery. Their ages will range from (40-60) years. They will be randomly divided into two equal groups: 1. Group A: This group will include 25 patients suffering from TMJ dysfunction (pain and reduced mouth opening) after tooth extraction. They will receive pulsed ultrasound and traditional manual therapy. The first session of treatment will be 24hr after extraction for three times for one week. 2. Group B: This group will include 25 patients suffering from TMJ dysfunction (pain and reduced mouth opening) after tooth extraction. They will receive virtual reality and traditional manual therapy. The first session of treatment will be 24hr after extraction for three times for one week.

Interventions

DEVICEultrasound

pulsed ultrasound

DEVICEvirtual reality

Fully Immersive VR

Sponsors

Amany Refaat Mohamed Abdel Wahid
Lead SponsorOTHER
Cairo University
CollaboratorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* The subject selection will be according to the following criteria: * Patients after tooth extraction. * Patients from both genders. * Patients suffering from pain and reduced mouth opening. * Age ranges between 40-60 years. * All patients will have informed consent.

Exclusion criteria

* . Surgery that conducted on the temporomandibular joint (meniscectomy, arthroscopy, etc.). * Patients with systemic disease as diabetes mellitus. * Patients with neurological conditions.

Design outcomes

Primary

MeasureTime frameDescription
pain free maximum mouth opening (MMO)before and after the treatment (after 1 week)Millimeter ruler for measuring pain free maximum mouth opening (MMO)
pain measurementbefore and after the treatment ( 1 week)Visual Analogue Scale for pain measurement (VAS).

Contacts

CONTACTAmany R M Abdel Wahid, Lecturer
amany.reffat.ar@cu.edu.eg+201018965528

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 9, 2026