Stroke Trial Flashcards

1
Q

What is this trial?

Patients with acute ischemic stroke <3hrs were randomized to IV t-PA (0.9mg/kg) or placebo and assessed for 4-point improvement in NIHSS or resolution of neurologic deficits within 24hrs. Clinical outcomes were also assessed at 3months.

Results:
No difference in neurologic outcome at 24hours.
At 3-months, patients given with IV t-PA have minimal or no disability.

A

NINDS T-PA Trial (National Institute of Neurological Disorders and Stroke t-PA) -1995

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2
Q

What is this trial?

Patients with acute ischemic stroke <6hours were randomized to t-PA at 1.1mg/kg

Results: No difference in disability using ITT. However, there were major protocol violations.

A

ECASS (European Australian Cooperative Acute Stroke Study)

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3
Q

What is this trial?

Patients with acute ischemic stroke <6hrs were randomized to rt-PA 0.9mg/kg or placebo.

Results: No significant difference in the rate of a favorable outcome at 3-months between t-PA and placebo-treated group.

A

ECASS-II

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4
Q

What is this trial?

Patients with acute ischemic stroke within 3 to 4.5hrs were randomized to rt-PA 0.9mg/kg or placebo.

Results: Significant more patients in rt-PA treated had favorable outcomes at 3 months (52.4% vs 45.2%). The incidence of intracranial hemorrhage was higher with rt-PA

A

ECASS- IIII (2008)

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5
Q

What is this trial?

Patients with acute ischemic stroke within 3hrs were given 0.6mg/kg IV rt-PA as single-arm, open-label study

Results: 36.9% achieved an mRS of 0 -1 at 3 months, symptomatic ICH occurred in 5.8%.

Data is comparable with published data using IV rt-PA.

A

Japanese Alteplase Clinical Trial (J-ACT)

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6
Q

What is this trial?

Patients with acute ischemic stroke within 4.5hours
who are eligible for thrombolytic therapy to low-dose intravenous alteplase (0.6 mg per kilogram of body weight) VS the standard dose (0.9 mg per kilogram).

Results:
Low-dose alteplase was noninferior in the ordinal analysis of modified Rankin scale scores (unadjusted common odds ratio, 1.00; 95% CI, 0.89 to 1.13; P=0.04 for noninferiority).
Major symptomatic intracerebral hemorrhage occurred in 1.0% of the participants in the low-dose group and in 2.1% of the participants in the standard-dose group (P=0.01); fatal events occurred within 7 days in 0.5% and 1.5%, respectively (P=0.01).
Mortality at 90 days did not differ significantly between the two groups (8.5% and 10.3%, respectively; P=0.07).

A

ENCHANTED Trial

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7
Q

What is this trial?

Patients with acute ischemic stroke within 6hrs were randomized to rt-PA 0.9mg/kg and placebo. No upper limit of age and broader BP eligibility.

Results:
The proportion of alive and independent at 6 months was 37% in the rTPA versus 35% in the placebo group
More deaths during 7 days.
At 6 months, 27% of patients died in both groups.

A

IST III (Third- International Stroke Trial)

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8
Q

What is CHANCE Trial?

A

Stroke patients within 24hrs of stroke
Mild ischemic stroke (NIHSS 0-5) or high risk TIA (ABCD2 > 3)
Clopidogrel 300mg then 75mg OD + Aspirin 75mg For 21 days then Clopidogrel 75mg alone for 90 days vs Aspirin75mg OD for 90 days.

Result: The rate of a recurrent stroke at 90 days were Aclopi-Aspi (8.2%) vs ASA alone (11.7%)

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9
Q

Which trial studies on Citicholine which showed global recovery at 90 days? (within 24hrs Citicholine 1000mg Q12 x 6 weeks)

A. ICTUS trial
B. CASTA trial
C. CATCH Trial
D. CHIMES Trial
E. CHANCE Trial
A

A. ICTUS trial

International Citicholine Trial on Acute Stroke

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10
Q

Which trial studies on Cerebrolysin showed no overall difference in outcomes between those who received Cerebrolysin in the placebo group at 90 days? (within 12hrs Cerebrolysin 30ml IV x 10 days)

A. ICTUS trial
B. CASTA trial
C. CATCH Trial
D. CHIMES Trial
E. CHANCE Trial
A

B. CASTA trial

(Cerebrolysin in Patients with Acute Ischemic Stroke in Asia

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11
Q

Which trial studies on NEUROAID showed a reduction in risk of recurrent fatal or non-fatal vascular events during 3 months of treatment? (within 72hrs Neuroaid 4caps TID x 90 days)

A. ICTUS trial
B. CASTA trial
C. CATCH Trial
D. CHIMES Trial
E. CHANCE Trial
A

D. CHIMES Trial

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12
Q

Among these neuroprotectants, which came from extract of nine herbal and five animal components in a capsule form?

A. Citicholine
B. Cerebrolysin
C. Amantadine
D. Neuroaid
E. Phosphatidylcholine
A

D. Neuroaid

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13
Q

Among these neuroprotectants, which is composed of low-molecular-weight peptides and free amino acids?

A. Citicholine
B. Cerebrolysin
C. Amantadine
D. Neuroaid
E. Phosphatidylcholine
A

B. Cerebrolysin

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14
Q

Among these neuroprotectants, which has a fullname of Cytidine 5’-diphosphate-choline (CDP-Choline)?

A. Citicholine
B. Cerebrolysin
C. Amantadine
D. Neuroaid
E. Phosphatidylcholine
A

A. Citicholine

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