Phase
Condition
Stroke
Thrombosis
Occlusions
Treatment
Remote Ischemic Conditioning with Novel Optical Sensor Feedback Device
Sham Remote Ischemic Conditioning with Novel Optical Sensor Feedback Device
Clinical Study ID
Ages 18-100 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Adult patients with ischemic stroke (anterior and posterior circulation involvement)with or without neurological deficit within 48h of symptom onset
CT head or MRI Brain evidence of infarct
CT head or MRI Brain evidence of moderate or severe small vessel disease. We willassess atrophy, leukoaraiosis and old vascular lesions.
Premorbid functional disability assessed by mRS <2
National institute of Health Stroke scale <15 at the time of enrollment
Exclusion
Exclusion Criteria:
Patient is part of other clinical trial delivering intervention
Injury to the upper arm or any other musculoskeletal disability/pain precluding fromtolerating RIC therapy
Treatment of ongoing malignancy with expected survival < 6 months
Presence of hypertensive urgency and emergency
Presence of hemodynamic instability
Presence of ongoing systemic infection with antibiotic therapy
Pregnant and lactating women
History of dermatological conditions affecting application of tissue perfusionsensor and remote ischemic conditioning pressure cuff
Study Design
Study Description
Connect with a study center
University of Alberta Hospital
Edmonton, Alberta T6G 2B7
CanadaSite Not Available
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