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Comparison · NCT01354197-sae

Survive at Day 28 vs Non-survive at Day 28: serious adverse events

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. Survive at Day 28 vs Non-survive at Day 28: serious adverse events. Trial comparisons, record NCT01354197-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01354197-sae

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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 10.2670.2530.281wilson
Risk in group 20.8080.7760.837wilson
Risk difference, group 1 minus group 2-0.542-0.573-0.506newcombe hybrid score
Risk ratio, group 1 over group 20.330.310.352log
Odds ratio, group 1 over group 20.08630.070.106log
Number needed to treat, for one fewer participant with a serious adverse event on Survive at Day 28 than on Non-survive at Day 281.851.741.97from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Survive at Day 28Number of participants who survive at day 281,0704,010EG000
Group 2Non-survive at Day 28Number of participants who Did Not survive at day 28519642EG001

Harm

What it counts
Total, serious adverse events
Time frame
Up to 28 days after surgical ICU admission

Source ClinicalTrials.gov

Trial

Title
The Thai Surgical Intensive Care Study (Thai-SICU Study)
NCT number
NCT01354197
Phases
Conditions
Complications of Surgical and Medical Care: General Terms, Adverse Reaction to Drug, Sequelae of External Causes of Morbidity and Mortality, Critical Illness
Interventions
Lead sponsor
Royal College of Anesthesiologists of Thailand
Results first posted
2017-03-27

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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