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Summary
To evaluate the dose-response of relevant blood biomarkers to remote ischemic conditioning in patients with age-related cerebral white matter hyperintensities on MRI, in preparation for a subsequent larger efficacy trial.
Eligible Conditions
- Cognitive Disorders
- White matter hyperintensities
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 5 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~5 weeks
Treatment Details
Study Objectives
Study objectives can provide a clearer picture of what you can expect from a treatment.Primary study objectives
RBC deformability index
Secondary study objectives
inflammatory and anti-inflammatory Interleukins
tolerability
Trial Design
5Treatment groups
Active Control
Placebo Group
Group I: dose 1Active Control1 Intervention
BP cuff bilateral arm compression to 50 mmHg above systolic BP for 2.5 minutes on/off for 4 cycles every other day.
Group II: dose 3Active Control1 Intervention
BP cuff bilateral arm compression to 50 mmHg above systolic BP for 5 minutes on/off once daily.
Group III: dose 2Active Control1 Intervention
BP cuff bilateral arm compression to 50 mmHg above systolic BP for 5 minutes on/off for 4 cycles every other day.
Group IV: dose 4Active Control1 Intervention
BP cuff bilateral arm compression to 50 mmHg above systolic BP for 5 minutes on/off twice daily.
Group V: shamPlacebo Group1 Intervention
BP cuff bilateral arm compression to 50 mmHg.
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Who is running the clinical trial?
Georgia Rehabilitation InstituteUNKNOWN
Augusta UniversityLead Sponsor
215 Previous Clinical Trials
85,650 Total Patients Enrolled
Carol Smith, RNStudy DirectorWellstar MCG Health
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