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Comparison · NCT03668236-0de99219

Fluid Restriction Group vs Standard-care: All-cause Mortality at 1-year After Randomisation

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. Fluid Restriction Group vs Standard-care: All-cause Mortality at 1-year After Randomisation. Trial comparisons, record NCT03668236-0de99219. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03668236-0de99219

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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 10.5130.4780.549wilson
Risk in group 20.4990.4640.535wilson
Risk difference, group 1 minus group 20.014-0.03630.0641newcombe hybrid score
Risk ratio, group 1 over group 21.030.9311.14log
Odds ratio, group 1 over group 21.060.8651.29log
Number needed to treat, for one more participant with the outcome on Fluid Restriction Group than on Standard-care71.5from 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 1Fluid Restriction GroupNo IV fluids unless one of the extenuating circumstances occurred (additional details in protocol section)385750OG000
Group 2Standard-careNo upper limit for IV fluids (additional details in protocol section).383767OG001

Outcome

Type
SECONDARY
Title
All-cause Mortality at 1-year After Randomisation
Description
Time frame
1-year after randomisation
Population

Source ClinicalTrials.gov

Trial

Title
The Conservative vs. Liberal Approach to Fluid Therapy of Septic Shock in Intensive Care Trial
NCT number
NCT03668236
Phases
PHASE4
Conditions
Septic Shock
Interventions
Isotonic crystalloids
Lead sponsor
Anders Perner, MD, PhD
Results first posted
2025-02-24

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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