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Clinical Trials in Canada / NCT06987747
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Reducing Pain in Complex Regional Pain Syndrome Using Personalized Brain Stimulation: A Feasibility Study

NCT06987747 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-07-01
Last updated
2025-05-23

Condition(s) studied

Complex Regional Pain Syndrome (CRPS)

Investigational drug(s) / intervention(s)

Repetitive transcranial magnetic stimulation

Repetitive transcranial magnetic stimulation: Repetitive transcranial magnetic stimulation (rTMS) is a non-invasive, non-painful procedure used to relieve chronic pain and promote short-term changes. The first dorsal interossei (FDI) muscle of the left motor cortex will be targeted using neuronavigation software. A series of 90 triplet pulses will be delivered at 100 Hz stimulation. Stimulation will be delivered at 80% of the resting motor threshold obtained from the right FDI muscle. The delivery of rTMS requires \~ 15 minutes in total.

Study summary

This research study looks at the feasibility of using a new treatment, noninvasively activating the brain through repetitive transcranial magnetic stimulation (rTMS) to treat pain symptoms of complex regional pain syndrome (CRPS). This study will help us determine if this technique is feasible (able to recruit participants and if the research activities are feasible and can be used to treat CRPS patients with pain in a larger study. The investigators will also examine how TMS can be personalized to individuals using an individual's brain activity measured using EEG. The investigators will also study whether the effects of TMS are stronger if the TMS is delivered during a specific timing of the EEG activity.

Eligibility

Sex
ALL
Min age
18 Years
Max age
70 Years
Healthy volunteers
No
Inclusion Criteria: * Diagnosis of CRPS Type 1 affecting the upper or lower limb using the revised Budapest criteria * History of CRPS of at least 3 months since the start of symptoms or diagnosis Exclusion Criteria: * CRPS diagnosis greater than 3 years to avoid patients with chronic CRPS who may not respond to interventions * Contraindications to transcranial magnetic stimulation (TMS) * Known psychological diagnosis affecting comprehension * Prior experience with TMS * Inability to participate in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
McMaster University Hamilton Ontario

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06987747 on ClinicalTrials.gov ↗ ← All trials in Canada