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Comparison · NCT03318783-6f31b4ba

GSK2256294 vs Placebo: Number of Participants With New Stroke on Hospital Discharge Imaging

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. GSK2256294 vs Placebo: Number of Participants With New Stroke on Hospital Discharge Imaging. Trial comparisons, record NCT03318783-6f31b4ba. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03318783-6f31b4ba

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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 10.10.01790.404wilson
Risk in group 20.1110.01990.435wilson
Risk difference, group 1 minus group 2-0.0111-0.3450.306newcombe hybrid score
Risk ratio, group 1 over group 20.90.065412.4log
Odds ratio, group 1 over group 20.8890.047416.7log
Number needed to treat, for one fewer participant with the outcome on GSK2256294 than on Placebo90from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1GSK2256294
10mg capsules of GSK2256294 will be administered in a single dose once daily enterally for a duration of 10 days.~GSK2256294: GSK2256294 will be administered in a single dose once daily enteral for a duration of 10 days.
110OG000
Group 2Placebo
10mg matched placebo capsules will be administered in a single dose once daily enterally for a duration of 10 days.~Placebo: Placebo will be administered in a single dose once daily enteral for a duration of 10 days.
19OG001

Outcome

Type
OTHER_PRE_SPECIFIED
Title
Number of Participants With New Stroke on Hospital Discharge Imaging
Description
The last head CT or other brain imaging to detect the presence of a new area of cerebral infarction will be reviewed at the time of hospital discharge. A cerebral infarction will be defined as a one identified on hospital discharge that was not present on imaging between 24-48 hours after aneurysm occlusion, and not attributable to other causes such as surgical clipping or endovascular treatment. Hypodensities resulting from extraventricular drains or residual intraparencyhmal hematomas will not be considered new strokes.
Time frame
90 days
Population

Source ClinicalTrials.gov

Trial

Title
Subarachnoid Hemorrhage and Soluble Epoxide Hydrolase Inhibition Trial
NCT number
NCT03318783
Phases
PHASE1, PHASE2
Conditions
Subarachnoid Hemorrhage, Aneurysmal, Delayed Cerebral Ischemia, Vasospasm, Cerebral, Endothelial Dysfunction
Interventions
GSK2256294, Placebo
Lead sponsor
Oregon Health and Science University
Results first posted
2021-01-22

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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