Clinical Trials Directory

Trials / Completed

CompletedNCT04157426

Percutaneous Electrolysis Versus Dry Needling in Levator Scapulae

Effectiveness of Ultrasound-guided Interventions of Percutaneous Electrolysis Versus Dry Needling in Levator Scapulae Active Myofascial Trigger Points

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
54 (actual)
Sponsor
Universidad Complutense de Madrid · Academic / Other
Sex
All
Age
18 Years – 70 Years
Healthy volunteers
Not accepted

Summary

The objective will be to determine the effectiveness of ultrasound-guided percutaneous electrolysis versus ultrasound-guided dry needling in active myofascial trigger points of the levator scapulae muscle on pain intensity, disability and range of motion. A randomized clinical trial will be carried out. Fifty-four patients with at least one active myofascial trigger point in the levator scapulae muscle were recruited and divided into ultrasound-guided percutaneous electrolysis (n = 27) and ultrasound-guided dry needling (n=27). Pain intensity, disability and range of motion will measured before, immediately after and 1 week after intervention.

Conditions

Interventions

TypeNameDescription
OTHERPercutaneous electrolysisUltrasound-guided percutaneous electrolysis in the active myofascial trigger point of the levator scapulae muscle
OTHERDry needlingUltrasound-guided dry needling the active myofascial trigger point of the levator scapulae muscle

Timeline

Start date
2021-09-28
Primary completion
2021-12-31
Completion
2022-01-01
First posted
2019-11-08
Last updated
2022-01-14

Locations

1 site across 1 country: Spain

Source: ClinicalTrials.gov record NCT04157426. Inclusion in this directory is not an endorsement.

Percutaneous Electrolysis Versus Dry Needling in Levator Scapulae (NCT04157426) · Clinical Trials Directory