The Importance of the Number of Incisions in the Effectiveness of Dry Needling
NCT ID: NCT06149442
Last Updated: 2024-10-16
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
RECRUITING
NA
90 participants
INTERVENTIONAL
2023-12-04
2025-09-20
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Dry needling consists of the use of a filiform needle to treat musculoskeletal pain. Currently, the mechanisms by which it is an effective technique are not well understood. One of the aspects not yet evaluated is the best dose in terms of the number of times it is necessary to insert the needle into the patient to achieve the best result.
This research work aims to assess which treatment obtains the best results in the management of patients with chronic neck pain.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Dry Needling Dosage in the Treatment of Myofascial Neck Pain
NCT02190890
Neurophysiological Effects of Dry Needling in Patients With Neck Pain
NCT03345238
Dry Needling of the Trapezius Muscle in Office Workers With Neck Pain
NCT02219386
Dry Needling Effectiveness and Post-punction Pain
NCT04148469
Effectiveness of Dry Needling and Ischemic Compression in Sternocleidomastoid, on Cervical Motor Control in Patients With Cervical Pain.
NCT03331653
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Randomly, the participants will be distributed to each of the treatment groups and we will measure how the effectiveness of each of the applied doses determines the result of the application of the dry needling technique in the treatment of neck pain.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
OTHER
TRIPLE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Dose of five muscle incisions
Subjects treated in this group will receive an in-out technique with a dosage of five incisions in the myofascial trigger point of the levator scapulae muscle.
Dose of five-incisions dry needling technique
Once we have assessed the existence of a myofascial trigger point in the levator scapulae muscle, and while the subject is in lateral decubitus on the same side, with a forceps palpation, we apply a rapid in /out dry needling technique (five incisions).
Dose of ten muscle incisions
Subjects treated in this group will receive an in-out technique with a dosage of ten incisions in the myofascial trigger point of the levator scapulae muscle.
Dose of ten-incisions dry needling technique
Once we have assessed the existence of a myofascial trigger point in the levator scapulae muscle, and while the subject is in lateral decubitus on the same side, with a forceps palpation, we apply a rapid in /out dry needling technique (ten incisions).
Dose of fifteen muscle incisions
Subjects treated in this group will receive an in-out technique with a dosage of fifteen incisions in the myofascial trigger point of the levator scapulae muscle.
Dose of fifteen-incisions dry needling technique
Once we have assessed the existence of a myofascial trigger point in the levator scapulae muscle, and while the subject is in lateral decubitus on the same side, with a forceps palpation, we apply a rapid in /out dry needling technique (fifteen incisions).
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
Dose of five-incisions dry needling technique
Once we have assessed the existence of a myofascial trigger point in the levator scapulae muscle, and while the subject is in lateral decubitus on the same side, with a forceps palpation, we apply a rapid in /out dry needling technique (five incisions).
Dose of ten-incisions dry needling technique
Once we have assessed the existence of a myofascial trigger point in the levator scapulae muscle, and while the subject is in lateral decubitus on the same side, with a forceps palpation, we apply a rapid in /out dry needling technique (ten incisions).
Dose of fifteen-incisions dry needling technique
Once we have assessed the existence of a myofascial trigger point in the levator scapulae muscle, and while the subject is in lateral decubitus on the same side, with a forceps palpation, we apply a rapid in /out dry needling technique (fifteen incisions).
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Neck pain of at least VAS 5/10.
* Reproduction of pain and symptoms subjects on palpation.
* Pain on passive stretching of the muscle.
Exclusion Criteria
* Subjects undergoing other intervention (rehabilitation/medication).
* Positive findings that raise suspicion of cervical radiculopathy:
* Subjects diagnosed: degenerative arthropathies, inflammatory, systemic conditions (fibromyalgia).
* Cardiovascular diseases.
* Whiplash or whiplash.
* Belenophobia.
* Dizziness and vertigo.
* Pregnant.
* Thyroid disorders.
18 Years
70 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
University of Alcala
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Prof. Dr. Daniel Pecos Martín
Principal investigator
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Daniel Pecos-Martin, PhD
Role: STUDY_DIRECTOR
Alcalá University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Centro Investigación Fisioterapia y Dolor
Alcalá de Henares, Madrid, Spain
Physiotherapy and Pain Institute
Alcalá de Henares, Madrid, Spain
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
CEIM/2022/1/008
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.