Evaluate the Effect of Dry Needling on the Temporomandibular Joint in Subjects Who Have Suffered a Whiplash as a Result of a Traffic Accident

NCT ID: NCT06023264

Last Updated: 2024-10-15

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

50 participants

Study Classification

INTERVENTIONAL

Study Start Date

2023-09-29

Study Completion Date

2024-09-30

Brief Summary

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The transportation industry is growing rapidly and the most popular mode is overland by road. Traffic accidents are the most direct and serious risk to the lives of Western people. A large number of traffic accidents occur on the roads each year, especially those caused by motor vehicles on motorways and urban ring roads, often resulting in massive loss of life. According to the World Health Organization (WHO), 1.35 million people die each year worldwide.

Whiplash is the most common injury in motor vehicle collisions, affecting 83% of injured people.

The temporomandibular joint (TMJ) is one of the most complex joints in the human body, since in addition to performing functions in dental occlusion, it does so in the neuromuscular system.

Due to the relationship of the neck with the mandible, the main objective of the study is to determine if there is an improvement in pain and functional limitation in general by applying the dry needling technique in the temporomandibular joint musculature.

Detailed Description

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Conditions

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Whiplash Temporomandibular Joint Pain Dry Needling Technique

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Control

Group Type NO_INTERVENTION

No interventions assigned to this group

dry needle

Group Type EXPERIMENTAL

Dry needling

Intervention Type PROCEDURE

It is a minimally invasive treatment modality. Its effectiveness has been confirmed in numerous studies. It consists of applying an antiseptic in the puncture area and inserting the needle in the required aseptic conditions. During puncture, the patient's physical response is observed at all times, in order to control the local spasmodic responses in each muscle. After applying the technique, we assessed jaw pain, mouth opening, and the appearance of headaches. The adverse effects of the technique are the following: pain after puncture (1.7%), local bleeding at the puncture site (6.1%) and syncopal responses (0.7%).

Interventions

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Dry needling

It is a minimally invasive treatment modality. Its effectiveness has been confirmed in numerous studies. It consists of applying an antiseptic in the puncture area and inserting the needle in the required aseptic conditions. During puncture, the patient's physical response is observed at all times, in order to control the local spasmodic responses in each muscle. After applying the technique, we assessed jaw pain, mouth opening, and the appearance of headaches. The adverse effects of the technique are the following: pain after puncture (1.7%), local bleeding at the puncture site (6.1%) and syncopal responses (0.7%).

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

* Having suffered a traffic accident
* Having suffered a subsequent collision
* Having been diagnosed with whiplash in the hospital ''Fundación Jiménez Díaz (FJD)´´ emergency room in the first 72 hours after the collision.
* Age between 18-45 years, to avoid osteoarthritis and other degenerative problems.
* Minimum 3 in temporomandibular joint (TMJ) according to Visual Analog Scale (VAS)
* Consent to participate

Exclusion Criteria

* Temporomandibular joint (TMJ) or craniofacial surgeries
* Spinal surgery
* Direct trauma in temporomandibular joint (TMJ) or prior to the accident
* Botox, silicones or any type of cosmetic surgery in the facial region.
* Problems of migraines and tension headaches (pre-accident)
* Any degenerative musculoskeletal disease (fibromyalgia, rheumatoid arthritis, osteoarthritis)
* Fear of needles
* Any neurological disorder (trigeminal neuralgia, epilepsy)
* Pregnancy
* Uncontrolled vascular or metabolic problems
Minimum Eligible Age

18 Years

Maximum Eligible Age

45 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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University of Alcala

OTHER

Sponsor Role collaborator

Instituto de Investigación Sanitaria de la Fundación Jiménez Díaz

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Universidad de Alcalá de Henares

Madrid, , Spain

Site Status

Patricia Recio Ramos

Madrid, , Spain

Site Status

Countries

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Spain

Other Identifiers

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03916375G

Identifier Type: -

Identifier Source: org_study_id

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