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Comparison · NCT00359424-e3e871d2

Endovascular Therapy vs IV Rt-PA Alone: Symptomatic Intracranial Hemorrhage

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

2 sourcestrial-comparisons-2026-03-23-0.1.0

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ConductScience Library. Endovascular Therapy vs IV Rt-PA Alone: Symptomatic Intracranial Hemorrhage. Trial comparisons, record NCT00359424-e3e871d2. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00359424-e3e871d2

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Measures6

Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.

MeasureValue95% interval, lower95% interval, upperMethodNote
Risk in group 10.06220.04310.089wilson
Risk in group 20.05860.03450.0976wilson
Risk difference, group 1 minus group 20.00365-0.03980.0396newcombe hybrid score
Risk ratio, group 1 over group 21.060.5592.02log
Odds ratio, group 1 over group 21.070.5392.11log
Number needed to treat, for one more participant with the outcome on Endovascular Therapy than on IV Rt-PA Alone274from the risk difference intervalthe interval includes no difference

Groups2

Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Endovascular Therapy
Group two will receive a lower dose or a standard dose of IV rt-PA and then undergo an angiogram test (cerebral angiography) right after the medicine is given to check for blood clots. If a clot is not seen then no more treatment will be given. If a clot is seen, the neurointerventionalist will then choose (based on the location and extent of the blood clot) a protocol approved endovascular treatment given directly in the brain artery that will be most effective in reopening the blocked artery.
27434OG000
Group 2IV Rt-PA AloneGroup one will receive the standard dose of intravenous (IV) rt-PA alone given over an hour.13222OG001

Outcome

Type
PRIMARY
Title
Symptomatic Intracranial Hemorrhage
Description
Symptomatic Intracranial Hemorrhage- Symptomatic ICH is defined as an intracranial hemorrhage temporally related to a decline in neurological status as well as new or worsening neurologic symptoms in the judgment of the clinical investigator and which may warrant medical intervention. These events are identified via Adverse Event CRF submitted by the site
Time frame
within the first 30 hours post IV rt-PA
Population
The intent-to-treat analysis sample includes all subjects who are randomized, and each subject is analyzed according to the treatment group to which they were randomly assigned.

Source ClinicalTrials.gov

Trial

Title
Interventional Management of Stroke (IMS) III Trial
NCT number
NCT00359424
Phases
PHASE3
Conditions
Stroke
Interventions
IV rt-PA alone, endovascular therapy
Lead sponsor
Joseph Broderick
Results first posted
2013-12-13

Source ClinicalTrials.gov

Source

Release
trial-comparisons-2026-03-23-0.1.0
Release manifest SHA-256
f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57
AACT copy
2026-03-23
Tables read
outcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquet

Source ClinicalTrials.gov

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions. The measures are ConductScience's calculation from them.

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