Skip to main content
OpenTrials
Completed

NCT Number: NCT06675149

Diacutaneus Fibrolysis on Tempromandibular Joint Pain and Trismus Post Oral Surgery

This study is carried out on sixty patients who will have tempromandibular pain and trismuspostOral and Maxillofacial Surgeryand their ages will be ranged from 18 to 40 years.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Temporomandibular Pain

Age range

18 year–40 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cairo University

Giza, 12613, Egypt

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Ages of patients will be ranged from 18 to 40 years.
  • All patients will have Oral and Maxillofacial Surgery.
  • All patients will be referred by a surgeon before starting the study procedure.
  • All participants will have pain and trismus in the jaw,
  • The participants will be also cleared for periodontal issues.
  • All patients will enter the study having their informed consent

Exclusion criteria

  • Patients with associated vascular injuries requiring arterial repair.
  • Patient with systemic diseases such as arthritis; pain attributable to confirmed migraine, head, or neck pain condition
  • Patient with acute infection or other significant disease of the teeth, ears, eyes, nose, or throat
  • Patient with present neurologic or cognitive deficit.
  • Patients with history of previously failed surgeries.

Treatment and study plan

Diacutaneus fibrolysis

Device

Material : Stainless steel large angle and small long angle: length 22cm x height 6cm x width 2cm. Weight: 70 grams

Other names: Hook measurements

Transcutaneous electrical nerve stimulation

Device

physical therapy electrical modality

Other names: TENS

Massage

Procedure

manual therapy intervention

Primary outcomes

  1. temporomandibular joint pain

    Time frame: pre intervention and re assessed after 1 month

    pain is assessed Pressure pain threshold(PPT) will be obtained with the aid of an algometer by applying pressure to the masseter and to the anterior, middle, and posterior temporalis, increasing pressure until the patient will feel that the pressure will become unpleasant or "painful .

  2. Trismus

    Time frame: pre intervention and re assessed after 1 month

    Trismus is assessed by caliper

Sponsors and collaborators

Lead sponsor

Cairo University

Other

Registry information

Official study title

Effect of Diacutaneus Fibrolysis on Tempromandibular Joint Pain and Trismus Post Oral and Maxillofacial Surgery

Important dates

Study start
2024
Primary completion
2024
Study completion
2025
First posted
Nov 5, 2024
Registry last updated
Mar 3, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Related clinical trials

Published trials that share one or more normalized conditions with this study.