Trial | NCT00975962  Report issue

Official Title

New Acute Treatment for Stroke - The Effect of Remote PERconditioning

  • Phase

    Phase 3

  • Study Type

    Interventional

  • Status

    Completed No Results Posted

  • Intervention/Treatment

    alteplase ...

  • Study Participants

    120
This study is a blinded randomized study. Randomization for treatment/not treatment with remote perconditioning takes place during transportation to the hospital. This is because the investigators' hypothesis states that remote perconditioning is neuro-protective and the effect is proportionally larger with early treatment. As the size of the effect is unknown, the investigators will use multiple magnetic resonance imaging (MRI) scans to determine the size of a potential neuro-protective effect.

The aims of this study are:

To describe method of remote perconditioning in clinical practice regarding feasibility. Pros and cons and potential limitations.
To estimate the size of the effect of remote perconditioning in combination with recombinant tissue plasminogen activator (rtPa) treatment within four and a half hours of onset of symptoms.
Final inclusion and informed consent takes place after first MRI in patients eligible for rtPA.

Follow-up MRI after 24h and 1 month. Clinical outcome at 3 months.
Study Started
Jul 31
2009
Primary Completion
Mar 31
2011
Study Completion
Mar 31
2011
Last Update
Jun 23
2011
Estimate

Drug Actilyse

Actilyse according to guidelines without pretreatment with remote persconditioning

Procedure Thrombolysis + remote perconditioning

The rIPerC consists of 4 cycles of 5 minute total occlusion of blood flow to the non-paretic arm separated by 5 minutes of reperfusion. The occlusion is secured by inflating a standard blood pressure cuff to 25 mmHg above the systolic blood pressure. Written instruction on cuff inflation and paramedic's documentation of their procedure were written in a standard report which was turned over to a study nurse upon arrival to the hospital, and filed. The investigators were hence blinded to the prehospital rIPerC.

Thrombolysis + Remote perconditioning Experimental

Remote perconditioning (rIPerC) undertaken in ambulance on rute to hospital in case of suspected stroke. The rIPerC consists of 4 cycles of 5 minute total occlusion of blood flow to the non-paretic arm separated by 5 minutes of reperfusion. The occlusion is secured by inflating a standard blood pressure cuff to 25 mmHg above the systolic blood pressure. Written instruction on cuff inflation and paramedic's documentation of their procedure were written in a standard report which was turned over to a study nurse upon arrival to the hospital, and filed. The investigators were hence blinded to the prehospital rIPerC.

Thrombolysis Active Comparator

Thrombolysis without pretreatment with remote perconditioning

Criteria 

Inclusion Criteria:

Significant ischemic stroke suspicion (NIHSS 1-24) and paresis of an extremity.
Treatment with rtPa within 4.5 hours from debut of symptoms.
Age above 18 (changed from 01.01.2010 to no upper age limit)
Independent in daily living before the acute onset of symptoms. (mrs</=2)
MR scan showing DWI lesion, consistent with acute ischemic stroke.

Exclusion Criteria:

Contraindications for iv rtPA
Onset of symptoms older than 4.5 hours
Previous diseases of the brain: Intracranial aneurisms or arteriovenous malformations. Brain surgery or hemorrhagic stroke. Former ischemic stroke within the last 3 months.
Heart diseases: Infectious endocarditis or suspicion of septic emboli, pericarditis, ventricular thrombosis, aneurisms of the heart wall or major heart failure.
Serious diseases: Cancer, AIDS, dementia, significant abuse, renal failure, liver diseases such as liver failure, cirrhosis, portal hypertension, active hepatitis.
Pregnancy
Major ischemic stroke where the patient is unconscious.(NIHSS > 25).
Symptoms suspect for migraine, Multiple sclerosis, TIA or another neurological disease than ischemic stroke.

MR scan:

Contraindications for MRI scans
Tumor cerebri, cerebral abscesses
Known hypersensitivity to Gadovist or any of its ingredients, acute or chronic severe renal impairment (GFR < 30 ml/min/1.73m2), acute renal insufficiency of any severity due to the hepato-renal syndrome or in the perioperative liver transplantation period.
Caution with using Gadovist to patients with severe cardiovascular disease, and only to be used after a risk-benefit assessment.
Caution with using Gadovist in patients with low threshold for seizures.

Lab data:

Blood glucose < 2, 8 mmol/l or > 22 mmol/l
No Results Posted