Analgesic Effects of Ultrasound-guided Dry-Needling Therapy for Neck and Head Pain
NCT ID: NCT03869710
Last Updated: 2024-12-03
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
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WITHDRAWN
NA
INTERVENTIONAL
2019-03-08
2023-12-25
Brief Summary
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Detailed Description
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The myofascial pain control will be assessed for the superficial and deep posterolateral muscle complex of neck. The analgesic request, Range Of Motion (ROM), Motion Related Pain (MRP) and the quality of life, will be also assessed.
Conditions
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Study Design
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NA
SINGLE_GROUP
TREATMENT
NONE
Study Groups
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Dry-Needling
Ultrasound-Guided Dry-Needling Therapy focused on the active and latent myofascial trigger points.
Ultrasound-guided Dry-Needling Therapy
The needle will be insert under ultrasound guidance to elicit the myofascial response on the neck of the patients
Interventions
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Ultrasound-guided Dry-Needling Therapy
The needle will be insert under ultrasound guidance to elicit the myofascial response on the neck of the patients
Eligibility Criteria
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Inclusion Criteria
* Chronic head pain
Exclusion Criteria
* Body Mass Index \> 39,99
* politrauma patients
* pregnancy
* neck and head infections
18 Years
85 Years
ALL
No
Sponsors
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San Salvatore Hospital of L'Aquila
OTHER
Responsible Party
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Emiliano Petrucci
Principal Investigator
Principal Investigators
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Pierfrancesco Fusco, MD
Role: PRINCIPAL_INVESTIGATOR
San Salvatore Academic Hospital
Locations
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San Salvatore Academic Hospital
Coppito, L'Aquila, Italy
Countries
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Other Identifiers
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0209913/17
Identifier Type: -
Identifier Source: org_study_id