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

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

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

JPRN

Registry ID

JPRN-UMIN000041286

Enrollment

Registered

2020-08-15

Start date

2019-02-18

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

chronic knee pain

Interventions

None listed

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: clonic knee patients without the indication of surgery

Exclusion criteria

Exclusion criteria: patients who are contraindicated to block procedure

Design outcomes

Primary

Measure	Time frame
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

Measure	Time frame
adverse events	—

Countries

Japan

Contacts

Public ContactAtsuko Hirano

Tokyo Metropolitan Bokutoh Hospital Department of Anesthesiology and Pain Clinic

hirano-a@umin.ac.jp03-3633-6151

Outcome results