Hemodynamic Effects on Cerebral Autoregulation in Acute Stroke

NCT ID: NCT02056821

Last Updated: 2017-01-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

88 participants

Study Classification

OBSERVATIONAL

Study Start Date

2014-02-28

Study Completion Date

2016-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

This study investigates if there are hemodynamic alterations in acute stroke that predispose patients to impaired perfusion and regulation of cerebral blood flow. To test this, we will target recruitment of acute ischemic stroke patients who present to the ED within 12 hours of symptoms onset. Enrolled subjects will receive continuous noninvasive hemodynamic monitoring contemporaneous with measurements of cerebral blood flow velocities and cerebral oximetry.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Ischemic Stroke

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Suspected ischemic stroke within 12 hours of symptom onset
* NIHSS ≥ 4
* Age 18 to 90 years

Exclusion Criteria

* Baseline modified Rankin Scale \> 3
* Pregnancy
* Intracranial hemorrhage on head CT
* Mechanical ventilation prior to enrollment
* Inadequate temporal windows for TCD analysis
Minimum Eligible Age

18 Years

Maximum Eligible Age

90 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Wayne State University

OTHER

Sponsor Role collaborator

Henry Ford Health System

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Joseph Miller, MD

Senior Staff

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Henry Ford Hospital

Detroit, Michigan, United States

Site Status

Countries

Review the countries where the study has at least one active or historical site.

United States

References

Explore related publications, articles, or registry entries linked to this study.

Miller J, Moloney JA, Elagamy N, Tuttle J, Tirgari S, Calo S, Thompson R, Nahab B, Lewandowski C, Levy P. Cerebral blood flow change with fluid resuscitation in acute ischemic stroke. Brain Circ. 2024 Dec 28;10(4):303-307. doi: 10.4103/bc.bc_30_24. eCollection 2024 Oct-Dec.

Reference Type DERIVED
PMID: 40012591 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

A20030

Identifier Type: -

Identifier Source: org_study_id

More Related Trials

Additional clinical trials that may be relevant based on similarity analysis.

Giessen Stroke Registry
NCT05295862 RECRUITING