Blood Pressure Lowering in Acute Stroke Trial

Withdrawn before enrolling · Phase 4 · Has a placebo group

Conditions studied: Stroke, Acute

In brief

The investigators hope to show that valsartan can be used safely in the setting of acute stroke to lower elevated blood pressure. There are novel properties of this class of drug (an angiotensive-receptor blocker or ARB), and promising human and animal data, that would suggest this drug can be safely used to lower blood pressure in the setting of acute stroke without compromising brain blood flow (i.e. cerebral perfusion). If this is proved to be the case, this compound could potentially be used routinely in this setting, with the hope of improving outcome. This pilot study may pave the way for a larger randomized trial looking at outcome measures in stroke patients. Further, a positive result in the this pilot study will serve as proof of concept that ARBs maintain cerebral perfusion while decreasing blood pressure, an overall favorable property.

Key facts

Study ID

NCT01400256

Run by

Stanford University

People needed

0

Starts

2007-08-01

Expected to finish

2009-02-01

Last updated by the study team

2016-05-09

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Men and non-pregnant women over age 18 who have had an acute ischemic stroke referable to the anterior circulation, as diagnosed by one of more of the following: clinical judgment, head CT, and/or MR imaging [i.e. a positive diffusion-weighted imaging (DWI) abnormality].
• Clinical syndrome not likely to represent transient ischemic attack (TIA) or other non-stroke etiology
• Patient must be neurologically stable at the time of first MRI scan (i.e. stable NIH Stroke Scale score).
• Initial MRI scan obtainable within 48 hours of symptom onset.
• A pre-existing diagnosis of hypertension, either treated or untreated.
• Average of two mean arterial blood pressures (separated by at least five minutes) at time of initial MRI scan ≥ 110.

You may not qualify if…

• Patients who have taken an angiotensin-converting enzyme (ACE) inhibitor or angiotensin receptor blocker (ARB) within seven (7) days of admission.
• Patients who received intravenous or intra-arterial r-TPA for their current symptoms, or those who underwent mechanical thrombolysis.
• Patients with hemorrhagic strokes, as seen on the initial head CT.
• Patients with stroke-like symptoms, but no demonstrable lesion on DWI, or a DWI lesion < 2 cm in diameter (greatest dimension).
• Patients with high-grade (>70%) internal carotid artery stenosis or occlusion ipsilateral to the current stroke.
• Patients with high-grade aortic or mitral stenosis.
• Patients with a previous adverse reaction to valsartan or other ARBs.
• Patients with contraindications for MRI, including pacemakers, claustrophobia, or severe obesity.
• Patients who are medically unstable for MR imaging, as determined by the treating team.
• Patients with a severe co-existing disease that may interfere with the conduct of the study.
• Patients receiving investigational drug therapies.
• Informed consent cannot be obtained from the patient or their legal representative.

Where it is running

• Stanford University Medical Center — Stanford, California, United States

Full record on ClinicalTrials.gov

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