Knee Pain Chronic Clinical Trial
Official title:
Efficacy of High and Low Intensity Percutaneous Electrolysis for the Treatment of Myofascial Pain Syndrome: A Pilot Study
Verified date | April 2020 |
Source | Universidad Francisco de Vitoria |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Muscle pain is frequently attributed to myofascial pain syndrome (MPS) in which myofascial
trigger points (MTrP) are a characteristic feature. Dry needling is a frequent clinical
practice to manage MPS but few evidence is published about percutaneous electrolysis effects
for the treatment of MPS.
This is a randomized clinical trial with 3 parallel groups: 1) High intensity-short time
percutaneous electrolysis; 2) Low intensity-long time percutaneous electrolysis; 3) dry
needling control group.
Status | Completed |
Enrollment | 15 |
Est. completion date | April 27, 2020 |
Est. primary completion date | March 30, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion Criteria: - Athletes with knee pain - Presence of at least one active Trigger point Exclusion Criteria: - Farmacologic treatment - Surgery or traumas - Skin alterations or infections - Prior 6 weeks DN nor PT treatment |
Country | Name | City | State |
---|---|---|---|
Spain | Camilo Jose Cela University | Villanueva de la Cañada | Madrid |
Lead Sponsor | Collaborator |
---|---|
Universidad Francisco de Vitoria |
Spain,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Pressure Pain Threshold (Trigger Point) | Algometry (Wagner analogical algometer) | 7 days | |
Primary | Pressure Pain Threshold (Patellar Tendon) | Algometry (Wagner analogical algometer) | 7 days | |
Secondary | Subjective pain perception | Visual Analogue Scale | 7 days |
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