Treatment of pain, anxiety and systolic blood pressure variability in patients hospitalized with acute stroke Signs and Symptoms
Conditions
Interventions
Eligible patients (or their legally authorized representative) were approached in the emergency department or obtained on admission to the inpatient ward and electronic consent. Staff not involved in
Sponsors
Michigan Medicine
Eligibility
Sex/Gender
All
Age
18 Years to 100 Years
Inclusion criteria
Inclusion criteria: Patients with acute stroke of any subtype admitted to the hospital within 24 hours of ictus
Exclusion criteria
Exclusion criteria: 1. Patients who refused consent 2. Patients at the end of life 3. Patients expected to have an operation or procedure
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. The percentage of eligible patients approached for consent who were recruited into the trial measured using data collected in study records at one timepoint 2. The percentage of enrolled patients who completed the 6-hour trial data collection measured using data collected in study records at one timepoint | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. The systolic blood pressure variability (SBPV) in the first 6 hours of the trial period, defined by the standard deviation of the SBP in the treatment arms, measured using cuff blood pressure measurements hourly 2. Secondary exploratory outcomes included the effect of treatment arm assignment (intention to treat) on the visual analog pain scale (0-10) and anxiety (visual analog scale 0-100) burden at 6 hours from enrollment | — |
Countries
United States of America
Contacts
Public ContactJeffrey Fletcher
Outcome results
None listed