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Comparison · NCT05327296-deaths

Isoflurane (Run-ins and Randomized) vs Propofol: deaths from any cause

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. Isoflurane (Run-ins and Randomized) vs Propofol: deaths from any cause. Trial comparisons, record NCT05327296-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT05327296-deaths

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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 10.3350.2690.409wilson
Risk in group 20.3910.2950.496wilson
Risk difference, group 1 minus group 2-0.0555-0.180.0651newcombe hybrid score
Risk ratio, group 1 over group 20.8580.6131.2log
Odds ratio, group 1 over group 20.7860.4611.34log
Number needed to treat, for one fewer death from any cause on Isoflurane (Run-ins and Randomized) than on Propofol18from 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 1Isoflurane (Run-ins and Randomized)Inhaled isoflurane administered via Sedaconda ACD-S~3-5 run-in patients treated with isoflurane were enrolled at each site prior to randomization58173EG000
Group 2PropofolPropofol administered as intravenous infusion~Propofol: Intravenous infusion of propofol3487EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse Events were collected from initiation of study drug administration until Day 7 post End Of Treatment (up to 9 days post treatment initiation). All-Cause Mortality was assessed for up to 6 months post randomization.

Source ClinicalTrials.gov

Trial

Title
Efficacy and Safety of Inhaled Isoflurane Delivered Via the Sedaconda ACD-S Compared to Intravenous Propofol for Sedation of Mechanically Ventilated Intensive Care Unit Adult Patients (INSPiRE-ICU2)
NCT number
NCT05327296
Phases
PHASE3
Conditions
Sedation
Interventions
Isoflurane, Propofol
Lead sponsor
Sedana Medical
Results first posted
2026-03-03

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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