ConductScience.org, home

Library / Trial comparisons

0.9% Sodium Chloride vs Balanced Crystalloids: deaths from any cause

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

Measures 6

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

MeasureValue95% interval, lower95% interval, upperMethodNoteSource
Risk in group 10.07830.07130.0859wilsonClinicalTrials.gov
Risk in group 20.07680.06990.0844wilsonClinicalTrials.gov
Risk difference, group 1 minus group 20.00143-0.008850.0117newcombe hybrid scoreClinicalTrials.gov
Risk ratio, group 1 over group 21.020.8921.16logClinicalTrials.gov
Odds ratio, group 1 over group 21.020.8841.18logClinicalTrials.gov
Number needed to harm, for one more death from any cause on 0.9% Sodium Chloride than on Balanced Crystalloids699from the risk difference intervalthe interval includes no differenceClinicalTrials.gov

Groups 2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov codeSource
Group 10.9% Sodium Chloride
Patients in an ICU block randomized to saline will receive 0.9% sodium chloride whenever isotonic intravenous crystalloid administration is ordered by the treating provider.~Saline: 0.9% sodium chloride will be used whenever an isotonic crystalloid is ordered
4085,214EG000ClinicalTrials.gov
Group 2Balanced Crystalloids
Patients in an ICU block randomized to balanced crystalloids will receive Plasma-Lyte A or Lactated Ringer's whenever isotonic intravenous crystalloid administration is ordered by the treating provider.~Balanced crystalloid: Lactated Ringers or Plasma-Lyte A will be used whenever an isotonic crystalloid is ordered
4005,207EG001ClinicalTrials.gov

Harm 2

FieldValueSource
What it countsTotal, all-cause mortalityClinicalTrials.gov
Time frame30 daysClinicalTrials.gov

Trial 8

FieldValueSource
TitleIsotonic Solutions and Major Adverse Renal Events Trial in the Non-Medical Intensive Care Unit (SMART-SURG)ClinicalTrials.gov
NCT numberNCT02547779ClinicalTrials.gov
PhasesNAClinicalTrials.gov
ConditionsCritical Illness, Acute Kidney InjuryClinicalTrials.gov
Interventions0.9% Saline, Physiologically-balanced isotonic crystalloidClinicalTrials.gov
Lead sponsorVanderbilt UniversityClinicalTrials.gov
Results first posted2019-11-25ClinicalTrials.gov
Results on ClinicalTrials.govhttps://clinicaltrials.gov/study/NCT02547779?tab=resultsClinicalTrials.gov

Source 4

FieldValueSource
Releasetrial-comparisons-2026-03-23-0.1.0ClinicalTrials.gov
Release manifest SHA-256f66225897fbf258b57ea10bdacfd0347d3cdfda93f7f5685234b7e06ea36fa57ClinicalTrials.gov
AACT copy2026-03-23ClinicalTrials.gov
Tables readoutcome_counts.parquet, outcome_measurements.parquet, outcomes.parquet, reported_event_totals.parquet, reported_events.parquet, result_groups.parquet, studies.parquet, ctgov_trial.parquetClinicalTrials.gov

The same record as JSON

Release trial-comparisons-2026-03-23-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.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.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.

ClinicalTrials.gov: none 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.