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
| Type | Name | Description |
|---|---|---|
| DEVICE | long-term paired associative stimulation | Paired 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)). |
| DEVICE | sham long-term paired associative stimulation | Sham 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.