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Comparison · NCT02251041-deaths

Combined Drug Approach vs Controles: 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. Combined Drug Approach vs Controles: deaths from any cause. Trial comparisons, record NCT02251041-deaths. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02251041-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 10.1110.04410.253wilson
Risk in group 20.08330.02870.218wilson
Risk difference, group 1 minus group 20.0278-0.1230.18newcombe hybrid score
Risk ratio, group 1 over group 21.330.3215.54log
Odds ratio, group 1 over group 21.380.2856.64log
Number needed to harm, for one more death from any cause on Combined Drug Approach than on Controles36from 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 1Combined Drug Approachthe group receives a combination of drugs~Antithrombin-III~Infliximab~Apotransferrin~Human recombinant erythropoietin~C1-Inhibitor~Glutathione~Alfa-tocopherol~Melatonin~Epoprostenol436EG000
Group 2Controlesthe group do not receive a combination of drugs, but a placebo (sodium chloride solution)~Sodium chloride solution336EG001

Harm

What it counts
Total, all-cause mortality
Time frame
Adverse events were collected over the time frame of 1 year starting immediately after transplantation

Source ClinicalTrials.gov

Trial

Title
Combined Drug Approach to Prevent Ischemia-reperfusion Injury During Transplantation of Livers (CAPITL)
NCT number
NCT02251041
Phases
PHASE2
Conditions
Reperfusion Injury
Interventions
Antithrombin-III, Infliximab, Apotransferrin, Human recombinant erythropoietin, C1-Inhibitor, Glutathione, Alfa-tocopherol, Melatonin, Epoprostenol, Sodium chloride solution
Lead sponsor
Universitaire Ziekenhuizen KU Leuven
Results first posted
2024-08-23

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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