Scrambler Therapy for Post-Stroke Pain

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorJohns Hopkins University

About this trial

The Investigators will enroll patients who have had a stroke and are experiencing post-stroke pain secondary to their infarct and disruption of the sensory system in a research study to compare the effectiveness of Scrambler Therapy to traditional pharmacologic therapies.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Men and women over the age of 18 with ischemic or hemorrhagic stroke seen on imaging and a positive finding for pain in the area(s) affected by their stroke location will be included.

The patients must be at least one month post-stroke but can otherwise enroll at any point.

Disqualifiers

Patients with TIA

Patients with no evidence of stroke on MRI

Patients with implantable devices such as pacemakers, defibrillators, spinal cord stimulators

Patients with history of myocardial infarction in the past 6 months

Trial design

Design model

Single group

Treatments tested in this trial

  • Scrambler Therapy for Post Stroke Pain

    Device

    All participants will either undergo either 5 or 10 treatments using Scrambler Therapy. The number of treatments will be decided by a randomization process.

Treatment groups

100 Participants
are divided into 1 treatment group
Group A: Scrambler TherapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Reduction in post stroke pain

At least a 50% reduction in post stroke pain

Time frame
6 months

Secondary outcomes

Other outcomes

Sponsors and contacts

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