Clinical Trials Directory

Trials / Completed

CompletedNCT05362422

PAS for Post-SCI Neuropathic Pain

Paired Associative Stimulation for Post- Spinal Cord Injury Neuropathic Pain

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
5 (actual)
Sponsor
Helsinki University Central Hospital · Academic / Other
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The investigators have shown in incomplete SCI patients that long-term paired associative stimulation is capable of restoring voluntary control over some paralyzed muscles and enhancing motor output in the weak muscles. In this study, the investigators will administer long-term paired associative stimulation to patients with incomplete cervical level SCI and SCI- associated neuropathic pain, and investigate its effectiveness for neuropathic pain treatment.

Conditions

Interventions

TypeNameDescription
DEVICElong-term paired associative stimulationPaired associative stimulation (PAS) administered 3-5 times per week for 4 weeks to upper limbs. PAS comprises transcranial magnetic stimulation (eXimia magnetic stimulator, Nexstim Ltd, Helsinki, Finland) and peripheral nerve stimulation (given with Dantec Keypoint® electroneuromyography device (Natus Medical Incorporated, Pleasanton, CA, USA)).
DEVICEsham long-term paired associative stimulationSham transcranial magnetic stimulation and sham peripheral nerve stimulation.

Timeline

Start date
2022-04-22
Primary completion
2023-05-22
Completion
2023-09-22
First posted
2022-05-05
Last updated
2023-09-25

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT05362422. Inclusion in this directory is not an endorsement.