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Efficacy and the safety of genicular nerveve pulsed radiofrequency treatment for Japanese patients

Not Applicable
Recruiting
Conditions
chronic knee pain
Registration Number
JPRN-UMIN000041286
Lead Sponsor
Tokyo Metropolitan Bokutoh Hospital
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

patients who are contraindicated to block procedure

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Inprovement of the pain score after the pulsed rediofrequency treatment; Numerical Rating Scale(NRS) one week after, 6 months after and 12 months after the treatment
Secondary Outcome Measures
NameTimeMethod
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