eurofeedback for phantom limb pai

Not Applicable

Recruiting

• Conditions: Phantom limb pain; D010591

• Registration Number: JPRN-jRCTs052220058
• Lead Sponsor: Yanagisawa Takufumi

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2022-06-28
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 10

Inclusion Criteria

(1) Age between 18 and 85 years old at the time of obtaining consent, regardless of gender and severity of illness
(2) Patients who have given written consent to participate in this study
(3) Patients with upper limb amputation or complete brachial plexus avulsion, who have no sensation in a single upper limb, phantom limb sensation and phantom pain.
(4) Patients who have phantom pain that interferes with their daily life for more than 3 months, although the intensity of phantom pain is not determined by VAS.

Exclusion Criteria

(1) Patients with a severe neurological dysfunction that makes it impossible to perform the task.
(2) Patients with serious underlying diseases other than the target disease
(3) Other patients for whom participation in this study is deemed inappropriate by the principal investigator or sub-investigator.
(4) Patients with implanted devices such as pacemakers

Study & Design

• Study Type: Interventional
• Study Design: Not specified