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Blood Pressure Variability in Acute Ischemic Stroke

Comparison of Blood Pressure Variability Indices and Ambulatory Arterial Stiffness Index as Prognostic Indicators in the Medium Term Outcome of Acute Ischemic Stroke

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01915862
Acronym
PREVISE
Enrollment
353
Registered
2013-08-05
Start date
2013-08-31
Completion date
2018-12-31
Last updated
2024-05-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Ischemic Stroke

Keywords

Acute ischemic stroke, Blood pressure variability, Ambulatory arterial stiffness index, Ambulatory blood pressure monitoring, Outcome

Brief summary

The purpose of this study is the evaluation and comparison of blood pressure variability indices and ambulatory arterial stiffness index obtained by ambulatory blood pressure monitoring as prognostic indicators in the functional outcome of acute ischemic stroke.

Detailed description

All consecutive patients admitted with acute (within 24 hours after stroke onset) ischemic stroke in three University Hospital of Northern and Central Greece will be included. Blood pressure measurements are being obtained with ambulatory 24-hour BP monitoring (ABPM) every 20 minutes within 24 hours of admission using automated oscillometric device (TM2430, A&D Company Ltd) during day-time (7:00-22:59) and night-time (23:00-6:59). Several clinical, laboratory and imaging parameters are prospectively registered. Also, patients' medical history, previous medical treatment and cardiovascular risk factors are registered. Functional outcome is assessed by the modified Rankin Scale score at 3 months. Also, stroke recurrence and cardiovascular and all-cause mortality will be assessed.

Interventions

None listed

Sponsors

A & D Company Limited
CollaboratorINDUSTRY
Aristotle University Of Thessaloniki
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Acute ischemic stroke * Admission within 24 after the onset of symptoms

Exclusion criteria

* Transient ischemic attack * Intracerebral hemorrhage * Subarachnoid hemorrhage * Cerebral sinus venous thrombosis * Stroke mimics * Late admission (\>24 hours after stroke onset)

Design outcomes

Primary

MeasureTime frameDescription
Modified Rankin Scale Score (mRS)Three months (90 days)Description (score) * No symptoms at all (0) * No significant disability despite symptoms; able to carry out all usual duties and activities (1) * Slight disability; unable to carry out all previous activities, but able to look after own affairs without assistance (2) * Moderate disability; requiring some help, but able to walk without assistance (3) * Moderately severe disability; unable to walk without assistance and unable to attend to own bodily needs without assistance (4) * Severe disability; bedridden, incontinent and requiring constant nursing care and attention(5) * Dead (6)

Countries

Greece

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 19, 2026