Clinical Trials Directory

Trials / Completed

CompletedNCT04101916

PAS in Subacute SCI

Paired Associative Stimulation in Subacute Spinal Cord Injury

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

Summary

The investigators have recently 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 at the subacute stage, and investigate its effectiveness for upper extremity rehabilitation.

Conditions

Interventions

TypeNameDescription
DEVICEPaired associative stimulationPaired associative stimulation (PAS) administered several times per week for 12 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 paired associative stimulationSham transcranial magnetic stimulation and sham peripheral nerve stimulation.

Timeline

Start date
2019-10-10
Primary completion
2025-01-13
Completion
2025-01-13
First posted
2019-09-24
Last updated
2025-03-13

Locations

1 site across 1 country: Finland

Source: ClinicalTrials.gov record NCT04101916. Inclusion in this directory is not an endorsement.