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Comparison · NCT02192502-sae

HES 130/0.4 (Voluven) vs Human Albumin 5%: 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. HES 130/0.4 (Voluven) vs Human Albumin 5%: serious adverse events. Trial comparisons, record NCT02192502-sae. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02192502-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 10.2460.160.36wilson
Risk in group 20.1670.0980.269wilson
Risk difference, group 1 minus group 20.0797-0.05440.212newcombe hybrid score
Risk ratio, group 1 over group 21.480.7632.86log
Odds ratio, group 1 over group 21.630.7153.74log
Number needed to harm, for one more participant with a serious adverse event on HES 130/0.4 (Voluven) than on Human Albumin 5%12.5from 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 1HES 130/0.4 (Voluven)6% HES 130/0.4 during surgery~HES 130/0.4 (Voluven)1769EG000
Group 2Human Albumin 5%human albumin 5% during surgery~human albumin 5%1272EG001

Harm

What it counts
Total, serious adverse events
Time frame
1 year

Source ClinicalTrials.gov

Trial

Title
Use of 6% Hydroxyethylstarch (130/0.4) in Cardiac Surgical Patients
NCT number
NCT02192502
Phases
PHASE3
Conditions
Postoperative Kidney Injury
Interventions
human albumin 5%, HES 130/0.4 (Voluven)
Lead sponsor
The Cleveland Clinic
Results first posted
2023-02-14

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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