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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COMPLETED
NA
28 participants
INTERVENTIONAL
2019-04-14
2019-11-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
DOUBLE
Study Groups
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Group 1: PNM in pain knee
participants in whom PNM will be applied to the femoral nerve of the pain knee
PNM
an asymmetric rectangular biphasic current (250 microseconds, 10 Hz)
Group 2: PNM in non-pain knee
participants in whom PNM will be applied to the femoral nerve of the non-pain knee
PNM
an asymmetric rectangular biphasic current (250 microseconds, 10 Hz)
Interventions
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PNM
an asymmetric rectangular biphasic current (250 microseconds, 10 Hz)
Eligibility Criteria
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Inclusion Criteria
* older than 18 years-old
Exclusion Criteria
* Prosthesis or osteosynthesis in the intervention area
* Cardiac or tumoral diseases
* Coagulopathies
* Be under the effects of certain medications
* contraindication characteristic of the puncture
18 Years
50 Years
ALL
No
Sponsors
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University of Seville
OTHER
Responsible Party
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Blanca de la Cruz Torres
Director
Locations
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University of Seville
Seville, , Spain
Countries
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Other Identifiers
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PNM and knee
Identifier Type: -
Identifier Source: org_study_id
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