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Effectiveness of Dry Needling as a Treatment of Shoulder Myofascial Pain Syndrome in Spinal Cord Injury Patients

U

Universidad de León

Status

Unknown

Conditions

Shoulder Pain
Puncture
Spinal Cord Injuries
Myofascial Pain Syndrome

Treatments

Procedure: Dry needling in infraspinatus muscle

Study type

Interventional

Funder types

Other

Identifiers

NCT03709797
ULeon-020-2018

Details and patient eligibility

About

Shoulder pain in people with spinal cord injury is one of the most prevalent in acute and chronic patients because of weakness in shoulder periarticular muscles, and also because of overuse of these part of the body in assistive devices.

This study aims to evidence if dry needling (a physiotherapy technique) is also useful in patients with spinal cord injury, and how long it could hold out without or less pain.

Enrollment

60 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • At least one year after Spinal Cord Injury (chronic patients).
  • Spinal Cord Injury under C5-C6 spinal level with American Spinal Injury Association (ASIA) classification.
  • Patients with shoulder pain and at least one active trigger point in infraspinatus muscle.

Exclusion criteria

  • Be apprehensive to the needles (belonephobia).
  • Immunosuppression.
  • Drug instability.
  • Other medical causes that, under medical prescription, dry needling in the shoulder are discouraged.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

60 participants in 2 patient groups

Experimental group
Experimental group
Description:
Experimental group will receive dry needling treatment.
Treatment:
Procedure: Dry needling in infraspinatus muscle
Control group
Sham Comparator group
Description:
Control group will receive sham dry needling treatment.
Treatment:
Procedure: Dry needling in infraspinatus muscle

Trial contacts and locations

1

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Central trial contact

Sandra Ms Palacios Alfonso

Data sourced from clinicaltrials.gov

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