Ultrasound Versus Virtual Reality on Temporomandibular Disorder
1 other identifier
interventional
50
0 countries
N/A
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.
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 May 2026
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
May 4, 2026
CompletedStudy Start
First participant enrolled
May 4, 2026
CompletedFirst Posted
Study publicly available on registry
May 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
July 15, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
July 30, 2026
May 8, 2026
May 1, 2026
2 months
May 4, 2026
May 4, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
pain free maximum mouth opening (MMO)
Millimeter ruler for measuring pain free maximum mouth opening (MMO)
before and after the treatment (after 1 week)
pain measurement
Visual Analogue Scale for pain measurement (VAS).
before and after the treatment ( 1 week)
Study Arms (2)
group who will receive ultrasound
ACTIVE COMPARATORThey will receive pulsed ultrasound and traditional manual therapy.
group who will receive virtual reality
ACTIVE COMPARATORthey will receive virtual reality and traditional manual therapy.
Interventions
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- Surgery that conducted on the temporomandibular joint (meniscectomy, arthroscopy, etc.).
- Patients with systemic disease as diabetes mellitus.
- Patients with neurological conditions.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Amany Refaat Mohamed Abdel Wahidlead
- Cairo Universitycollaborator
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- PARTICIPANT
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR INVESTIGATOR
- PI Title
- Lecturer at faculty of physical therapy Cairo University
Study Record Dates
First Submitted
May 4, 2026
First Posted
May 8, 2026
Study Start
May 4, 2026
Primary Completion (Estimated)
July 15, 2026
Study Completion (Estimated)
July 30, 2026
Last Updated
May 8, 2026
Record last verified: 2026-05
Data Sharing
- IPD Sharing
- Will not share