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Head Position in Stroke Trial (HeadPoST-Pilot)

Primary Purpose

Ischemic Stroke

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Head Position
Sponsored by
Clinica Alemana de Santiago
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Ischemic Stroke focused on measuring stroke, head position

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 or more years old
  • Patients with an acute stroke corresponding to anterior circulation, a CT scan ruling out intracranial hemorrhage, presenting within 12 hours from symptom onset
  • NIHSS ≥1
  • Susceptible to be tilted down to the flat position or to 30º of the head
  • There is uncertainty about the benefit/harm of head position during a minimum of 24 hours.
  • Informed consent given

Exclusion Criteria:

  • Contraindications to a flat head position (active vomiting, pneumonia, uncontrolled heart failure)
  • Concomitant medical illness that would interfere with outcome assessment and follow-up
  • Planned decompressive craniectomy or carotid endarterectomy.
  • Absence of sonographic temporal window

Sites / Locations

  • Royal Prince Alfred Hospital
  • Hospital regional Dr. Lautaro Navarro Avaria
  • Clinica Alemana de Santiago

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

lying flat head position

Arm Description

positioning the head of the bed at zero degrees during the first 48 hours from admission of patients with acute ischemic stroke Active Comparator: upright position of the head of the bed during 48 hours from admission of patients with acute ischemic stroke

Outcomes

Primary Outcome Measures

Increased mean cerebral blood flow velocity (CBFV) in the lying flat compared to the upright head position
The main efficacy outcome of the pilot phase is demonstration of increased mean cerebral blood flow velocity (CBFV) in the lying flat head position compared to the upright head position, as assessed by transcranial Doppler (TCD) to the medial cerebral arteries of patients with anterior circulation infarction.

Secondary Outcome Measures

proportion of Serious adverse events.
Assessments of Serious adverse events at 7 days comparing between the two head positioning groups.

Full Information

First Posted
October 11, 2012
Last Updated
December 2, 2015
Sponsor
Clinica Alemana de Santiago
Collaborators
The George Institute
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1. Study Identification

Unique Protocol Identification Number
NCT01706094
Brief Title
Head Position in Stroke Trial
Acronym
HeadPoST-Pilot
Official Title
Head Position in Stroke Trial
Study Type
Interventional

2. Study Status

Record Verification Date
December 2015
Overall Recruitment Status
Completed
Study Start Date
January 2013 (undefined)
Primary Completion Date
July 2015 (Actual)
Study Completion Date
October 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Clinica Alemana de Santiago
Collaborators
The George Institute

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
A simplest manner to augment cerebral blood flow to irrigate the ischemic penumbra in acute ischemic stroke could be to place the patient in a 'lying flat' rather than upright head position. Given uncertainty over the balance of potential modest benefits and risks, and variability regarding the ideal head position policy for patients with acute ischemic stroke around the world, reliable randomized evidence is required to standardize clinical practice. The main objectives of this pilot phase clinical trial are to determine the feasibility, safety and potential efficacy of a large-scale cluster randomized clinical trial to assess whether a simple nursing care policy - 'lying flat head position' - provides beneficial effects as compared to the standard upright head position in patients with acute ischemic stroke. The main efficacy outcome of the pilot phase is demonstration of increased mean cerebral blood flow velocity in the flat down compared to the upright head position, as assessed by transcranial Doppler to the medial cerebral arteries of patients with anterior circulation infarction. Secondary efficacy objectives are to demonstrate that the flat down head position improves neurological status at 7 days and disability at 90 days.
Detailed Description
Background: Several lines of investigation indicate there to be potential beneficial effects of interventions that augment cerebral blood flow (CBF) to irrigate the ischemic penumbra in acute ischemic stroke. The simplest manner to do this is to place the patient in a 'lying flat' rather than upright head position. However, any potential benefits on the brain may be offset by an increased hazard of aspiration pneumonia or exacerbation of cardiac failure in vulnerable patients. Given uncertainty over the balance of potential modest benefits and risks, and variability regarding the ideal head position policy for patients with acute ischemic stroke around the world, reliable randomized evidence is required to standardize clinical practice. Aims: The main objectives of this pilot phase clinical trial are to determine the feasibility, safety and potential efficacy of a large-scale cluster randomized clinical trial to assess whether a simple nursing care policy - 'lying flat head position' - provides beneficial effects as compared to the standard upright head position in patients with acute ischemic stroke. The main efficacy outcome of the pilot phase is demonstration of increased mean cerebral blood flow velocity (CBFV) in the lying flat head position compared to the upright head position, as assessed by transcranial Doppler (TCD) to the medial cerebral arteries of patients with anterior circulation infarction. Secondary efficacy objectives are to demonstrate that the lying flat head position improves neurological status at 7 days and disability at 90 days. Methods: Inclusion criteria include consecutive adult patients with acute ischemic stroke within 12 hours of onset admitted to participating centers. A cluster (month) method of randomization to lying flat or upright head position for 48 hours, stratified by site The primary outcome is change in mean CBFV measured by TCD at 24 hours. Secondary outcomes include proportion of adverse events at 7 days, distribution of NIHSS at 7 days, and distribution of mRS disability scale scores at 90 days. Sample size is 46 clusters of 2 patients totaling approximately 92 patients to detect an increase of 8.31 (CI 95% 4.82-12.0) cm/sec in average CBFV from 30° to 0° head position. This sample size will also allow detection of that difference with 90% power at a 5% significance level, considering an ICC of 0.037.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ischemic Stroke
Keywords
stroke, head position

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
Outcomes Assessor
Allocation
N/A
Enrollment
92 (Actual)

8. Arms, Groups, and Interventions

Arm Title
lying flat head position
Arm Type
Experimental
Arm Description
positioning the head of the bed at zero degrees during the first 48 hours from admission of patients with acute ischemic stroke Active Comparator: upright position of the head of the bed during 48 hours from admission of patients with acute ischemic stroke
Intervention Type
Other
Intervention Name(s)
Head Position
Intervention Description
Head position during the first 48 hours from admission of patients with acute ischemic stroke. This trial is organized as a cluster randomised trial to a policy of flat head position or upright head position. Clusters will be months, so that all patients admitted during a given month will be positioned either in the flat down head position (intervention) or upright head position (control). This will allow health teams to follow a monthly protocol without changing position between patients.
Primary Outcome Measure Information:
Title
Increased mean cerebral blood flow velocity (CBFV) in the lying flat compared to the upright head position
Description
The main efficacy outcome of the pilot phase is demonstration of increased mean cerebral blood flow velocity (CBFV) in the lying flat head position compared to the upright head position, as assessed by transcranial Doppler (TCD) to the medial cerebral arteries of patients with anterior circulation infarction.
Time Frame
24 hours
Secondary Outcome Measure Information:
Title
proportion of Serious adverse events.
Description
Assessments of Serious adverse events at 7 days comparing between the two head positioning groups.
Time Frame
7 days
Other Pre-specified Outcome Measures:
Title
Functional outcomes
Description
Secondary efficacy outcome are to demonstrate that the lying flat head position improves neurological status at 7 days and disability at 90 days, measured by modified Rankin Scale, in person or by telephone.
Time Frame
7 days and 90 days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 or more years old Patients with an acute stroke corresponding to anterior circulation, a CT scan ruling out intracranial hemorrhage, presenting within 12 hours from symptom onset NIHSS ≥1 Susceptible to be tilted down to the flat position or to 30º of the head There is uncertainty about the benefit/harm of head position during a minimum of 24 hours. Informed consent given Exclusion Criteria: Contraindications to a flat head position (active vomiting, pneumonia, uncontrolled heart failure) Concomitant medical illness that would interfere with outcome assessment and follow-up Planned decompressive craniectomy or carotid endarterectomy. Absence of sonographic temporal window
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Veronica V Olavarria, MD, Msc
Organizational Affiliation
Clinica Alemana de Santiago, Chile.
Official's Role
Study Director
Facility Information:
Facility Name
Royal Prince Alfred Hospital
City
Sydney
State/Province
New South Wales
Country
Australia
Facility Name
Hospital regional Dr. Lautaro Navarro Avaria
City
Punta Arenas
State/Province
Region de Magallanes
Country
Chile
Facility Name
Clinica Alemana de Santiago
City
Santiago
State/Province
Region Metropolitana
Country
Chile

12. IPD Sharing Statement

Citations:
PubMed Identifier
28581366
Citation
Olavarria VV, Lavados PM, Munoz-Venturelli P, Gonzalez F, Gaete J, Martins S, Arima H, Anderson CS, Brunser AM. Flat-head positioning increases cerebral blood flow in anterior circulation acute ischemic stroke. A cluster randomized phase IIb trial. Int J Stroke. 2018 Aug;13(6):600-611. doi: 10.1177/1747493017711943. Epub 2017 Jun 5.
Results Reference
derived
PubMed Identifier
27742914
Citation
Olavarria VV, Arima H, Anderson CS, Brunser A, Munoz-Venturelli P, Billot L, Lavados PM; HEADPOST Pilot Investigators. Statistical analysis plan of the head position in acute ischemic stroke trial pilot (HEADPOST pilot). Int J Stroke. 2017 Feb;12(2):211-215. doi: 10.1177/1747493016674955. Epub 2016 Oct 14.
Results Reference
derived
PubMed Identifier
26783317
Citation
Brunser AM, Munoz Venturelli P, Lavados PM, Gaete J, Martins S, Arima H, Anderson CS, Olavarria VV. Head position and cerebral blood flow in acute ischemic stroke patients: Protocol for the pilot phase, cluster randomized, Head Position in Acute Ischemic Stroke Trial (HeadPoST pilot). Int J Stroke. 2016 Feb;11(2):253-9. doi: 10.1177/1747493015620808.
Results Reference
derived

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Head Position in Stroke Trial

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