- ICH GCP
- Register voor klinische proeven in de VS.
- Klinische proef NCT01138059
Reperfusion Therapy in Acute Ischemic Stroke With Unclear Onset (RESTORE)
4 juni 2010 bijgewerkt door: Asan Medical Center
REperfusion Therapy in Acute Ischemic STroke With Unclear Onset by MRI Evaluation
This study will test the hypothesis whether patients with unclear-onset stroke (UnCLOS) treated with thrombolysis could achieve a prespecified rate of good clinical outcome.
The secondary hypothesis is that the efficacy outcomes in UnCLOS group would be superior to those in historical UnCLOS group from prospective stroke registries.
Studie Overzicht
Toestand
Voltooid
Conditie
Gedetailleerde beschrijving
- Study design: A prospective multicenter trial
- Study centers: 6 participating medical centers in South Korea
- Participants: Consecutive patients with acute ischemic stroke visiting the emergency room within 6 hours of the detection of stroke symptoms
Methods
3 thrombolysis protocols applicable to UnCLOS patients
- IV tissue plasminogen activator (tPA) : Conventional intravenous tPA (0.9 mg/kg, 10% of the dose as a bolus and the remainder over 60 minutes) will be administered to patients within 3 hours of first found abnormal time who had no arterial occlusion or catheter-inaccessible occlusion.
- IV tPA + IA urokinase protocol : Combined intravenous tPA (0.6 mg/kg, 10% of the dose as a bolus and the remainder over 30 minutes) with intra-arterial urokinase will be administered to those within 3 hours from first found abnormal time who had catheter-accessible arterial occlusion.
- IA UK protocol : Intra-arterial urokinase will be given to those between 3 and 6 hours after first found abnormal time who had catheter-accessible arterial occlusion.
Outcome variables
- Safety outcomes Symptomatic intracranial hemorrhage (ICH) within 48 hours from thrombolytic therapy.
Efficacy outcomes
- Long-term clinical outcomes (modified Rankin Scale) at 3 months
- Secondary efficacy outcomes : Good vs. Poor outcomes according to mRS responder analysis, Early neurological improvement, Immediate and 5-day recanalization on MRA or CTA
Studietype
Observationeel
Inschrijving (Werkelijk)
83
Deelname Criteria
Onderzoekers zoeken naar mensen die aan een bepaalde beschrijving voldoen, de zogenaamde geschiktheidscriteria. Enkele voorbeelden van deze criteria zijn iemands algemene gezondheidstoestand of eerdere behandelingen.
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
18 jaar tot 85 jaar (Volwassen, Oudere volwassene)
Accepteert gezonde vrijwilligers
Nee
Geslachten die in aanmerking komen voor studie
Allemaal
Bemonsteringsmethode
Niet-waarschijnlijkheidssteekproef
Studie Bevolking
Consecutive patients with acute ischemic stroke visiting the ER within 6 hours of the detection of stroke symptoms will be screened for this study.
Beschrijving
Inclusion Criteria:
- The patient is male or female and age between 18 and 85 years
- The patient has unclear onset stroke
- Treatment of the patient can be initiated within 6 hours after first found abnormal time
- The patient has imaging-defined penumbra (at least 20%), measured by diffusion- and perfusion-weighted MRI
Exclusion Criteria:
- The patient has minor neurologic deficits (NIHSS <4, except aphasia or hemianopia).
- The patient has rapidly resolving neurological symptoms and the rate of improvement is projected to give the patient an NIHSS score <4 at the time of treatment.
- The patient has a pre-stroke mRS score of >1 (indicating previous disability).
- The symptoms of stroke are suggestive of subarachnoid hemorrhage.
- Evidence of infective endocarditis or septic embolism
- The patient has a history or clinical presentation of ICH, SAH, or AVM.
- Serious head trauma within 6 weeks
- Prior ischemic stroke in previous 6 weeks (except small infarct)
- Myocardial infarction in the previous 3 weeks
- Gastrointestinal or urinary tract bleeding in previous 21 days
- Major surgery in the previous 14 days
- History of biopsy of a parenchymal organ, trauma with internal organ injury or lumbar puncture within 14 days
- Arterial puncture at a non-compressible site in the previous 7 days
- Uncontrolled high blood pressure (systolic > 185 mmHg or diastolic > 110 mmHg on 3 separate occasions at least 10 min apart despite appropriate treatment)
- Evidence of active bleeding or acute trauma (fracture) on examination
- Current use of oral anticoagulants and a prolonged prothrombin time (INR >1.7)
- The patient has been treated with heparin in the previous 48 hours with prolonged aPTT, except for low dose subcutaneous LMWH with doses recommended for DVT prophylaxis
- Baseline platelet count < 100,000 mm3
- Baseline hematocrit < 25%
- Blood glucose concentration < 50 mg/dL (2.7 mmol/L) in case of CT screening
- Seizure at onset with postictal residual neurological impairments in case of CT screening
- The patient has a terminal illness.
- The patient is, in the opinion of the investigator, unlikely to comply with the clinical study protocol or is unsuitable for any other reason.
- The patient has extensive early infarction in any affected area defined as an infarcted core involving > 1/3 of MCA territory or the entire ACA or PCA territory
- The patient has well-developed parenchymal hyperintensity on FLAIR, T2*, or EPI-T2 images, or marked hypodensity on CT, indicative of subacute infarction, or enhancement with morphologic features suggesting the lesion is more than 6 hours old
- The patient has a contraindication to the imaging techniques (this means ferromagnetic objects for MRI, contraindications to contrast agent, renal disease with iodinated contrast agent in perfusion CT and CTA, etc.)
- The patient has imaging evidence of ICH or SAH, AVM, brain tumor (Incidental meningioma and microbleeds are not exclusion criteria. Incidental unruptured aneurysm that is small (< 5mm) is not an exclusion criterion).
Studie plan
Dit gedeelte bevat details van het studieplan, inclusief hoe de studie is opgezet en wat de studie meet.
Hoe is de studie opgezet?
Ontwerpdetails
Cohorten en interventies
Groep / Cohort |
|---|
|
Acute ischemic stroke patients with unclear onset
|
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Tijdsspanne |
|---|---|
|
Good clinical outcome defined as modified Rankin Scale 0-2
Tijdsspanne: 3 months after treatment
|
3 months after treatment
|
|
Symptomatic intracranial hemorrhage
Tijdsspanne: 48 hours after treatment
|
48 hours after treatment
|
Medewerkers en onderzoekers
Hier vindt u mensen en organisaties die betrokken zijn bij dit onderzoek.
Sponsor
Medewerkers
Studie record data
Deze datums volgen de voortgang van het onderzoeksdossier en de samenvatting van de ingediende resultaten bij ClinicalTrials.gov. Studieverslagen en gerapporteerde resultaten worden beoordeeld door de National Library of Medicine (NLM) om er zeker van te zijn dat ze voldoen aan specifieke kwaliteitscontrolenormen voordat ze op de openbare website worden geplaatst.
Bestudeer belangrijke data
Studie start
1 oktober 2006
Primaire voltooiing (Werkelijk)
1 juni 2009
Studie voltooiing (Werkelijk)
1 juni 2009
Studieregistratiedata
Eerst ingediend
4 juni 2010
Eerst ingediend dat voldeed aan de QC-criteria
4 juni 2010
Eerst geplaatst (Schatting)
7 juni 2010
Updates van studierecords
Laatste update geplaatst (Schatting)
7 juni 2010
Laatste update ingediend die voldeed aan QC-criteria
4 juni 2010
Laatst geverifieerd
1 oktober 2006
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- AMC-2004-217
Deze informatie is zonder wijzigingen rechtstreeks van de website clinicaltrials.gov gehaald. Als u verzoeken heeft om uw onderzoeksgegevens te wijzigen, te verwijderen of bij te werken, neem dan contact op met register@clinicaltrials.gov. Zodra er een wijziging wordt doorgevoerd op clinicaltrials.gov, wordt deze ook automatisch bijgewerkt op onze website .