NCT07575633

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

65
Monitor

Trial Health Score

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

Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
3mo left

Started May 2026

Shorter than P25 for not_applicable

Status
not yet recruiting

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 Progress6%
May 2026Jul 2026

First Submitted

Initial submission to the registry

May 4, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

May 4, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

May 8, 2026

Completed
2 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

July 15, 2026

Expected
15 days until next milestone

Study Completion

Last participant's last visit for all outcomes

July 30, 2026

Last Updated

May 8, 2026

Status Verified

May 1, 2026

Enrollment Period

2 months

First QC Date

May 4, 2026

Last Update Submit

May 4, 2026

Conditions

Keywords

Temporomandibular disorderUltrasoundVirtual Realitysurgery

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 COMPARATOR

They will receive pulsed ultrasound and traditional manual therapy.

Device: ultrasound

group who will receive virtual reality

ACTIVE COMPARATOR

they will receive virtual reality and traditional manual therapy.

Device: virtual reality

Interventions

pulsed ultrasound

group who will receive ultrasound

Fully Immersive VR

group who will receive virtual reality

Eligibility Criteria

Age40 Years - 60 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64)

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

MeSH Terms

Conditions

Temporomandibular Joint Disorders

Interventions

Ultrasonography

Condition Hierarchy (Ancestors)

Craniomandibular DisordersMandibular DiseasesJaw DiseasesMusculoskeletal DiseasesJoint DiseasesMuscular DiseasesStomatognathic Diseases

Intervention Hierarchy (Ancestors)

Diagnostic ImagingDiagnostic Techniques and ProceduresDiagnosis

Central Study Contacts

Amany R M Abdel Wahid, Lecturer

CONTACT

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