Trials / Not Yet Recruiting
Not Yet RecruitingNCT06966128
Transcranial Electrical Stimulation in Multiple Sclerosis
The Effect of Transcranial Direct Current Stimulation on Cerebral Blood Flow in Patients With Multiple Sclerosis
- Status
- Not Yet Recruiting
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 100 (estimated)
- Sponsor
- Universitair Ziekenhuis Brussel · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Accepted
Summary
First the investigators will examine if the blood flow in the brain is different in patients with Multiple Sclerosis compared to healthy volunteers. HOW? \- The blood flow of the subjects is imaged by use of a special MRI-technique. Secondly, the investigators will examine if the blood flow can determine disease progression. HOW? - Multiple Sclerosis patients are asked for a follow-up visit after two years. The main goal is to understand the effect of transcranial Direct Current Stimulation (tDCS) on the cerebral blood flow. * Does tDCS result in a different blood flow, in which brain regions? * Is there a difference between healthy volunteers and Multiple Sclerosis patients? HOW? \- Participants get two session of tDCS. Before, during and after stimulation MRI scans are performed.
Detailed description
Comparison of CBF between healthy volunteers and MS patients: \- Arterial spin labelling (ASL) is used to investigate cerebral blood flow in patients with MS and healthy volunteers. The effect of transcranial direct current stimulation (tDCS) on cerebral blood flow: * ASL scans are performed before-, during-, and after tDCS * Each subject will receive active and sham tDCS (seperated by at least two days) (cross-over design). Follow-up visit: * After two years, patients with MS are re-invited. * This visit will include a new neuropsychological evaluation, blood sampling and additional brain scans.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | transcranial Direct Current Stimulation | Stimulation intensity: Variable (between 1 mA and 2 mA), Electrode placement: Dorsolateral prefrontal cortex, Duration: 10 minutes |
Timeline
- Start date
- 2025-06-01
- Primary completion
- 2029-01-01
- Completion
- 2029-01-01
- First posted
- 2025-05-11
- Last updated
- 2025-05-29
Locations
2 sites across 1 country: Belgium
Regulatory
- FDA-regulated device study
Source: ClinicalTrials.gov record NCT06966128. Inclusion in this directory is not an endorsement.