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Comparison · NCT02940860-81636dce

Iron Isomaltoside/Ferric Derisomaltose vs Iron Sucrose: Composite Cardiovascular Adverse Events (AEs)

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. Iron Isomaltoside/Ferric Derisomaltose vs Iron Sucrose: Composite Cardiovascular Adverse Events (AEs). Trial comparisons, record NCT02940860-81636dce. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02940860-81636dce

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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 10.04120.03060.0552wilson
Risk in group 20.06920.05020.0947wilson
Risk difference, group 1 minus group 2-0.028-0.0556-0.00432newcombe hybrid score
Risk ratio, group 1 over group 20.5960.3850.921log
Odds ratio, group 1 over group 20.5790.3650.918log
Number needed to treat, for one fewer participant with the outcome on Iron Isomaltoside/Ferric Derisomaltose than on Iron Sucrose35.818231from the risk difference interval

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Iron Isomaltoside/Ferric DerisomaltoseIron isomaltoside/ferric derisomaltose, administered IV421,019OG000
Group 2Iron SucroseIron sucrose, administered IV35506OG001

Outcome

Type
SECONDARY
Title
Composite Cardiovascular Adverse Events (AEs)
Description
Safety~Results show the composite cardiovascular AEs, that started on or after the first dose of randomised treatment (i.e. treatment emergent) up to week 8.~The reported potential cardiovascular AEs were adjudicated in a blinded fashion by an independent Clinical Endpoint Adjudication Committee (CEAC).~The potential cardiovascular AEs included the following:~* Death due to any cause~* Non-fatal myocardial infarction~* Non-fatal stroke~* Unstable angina requiring hospitalisation~* Congestive heart failure requiring hospitalisation or medical intervention~* Arrhythmias~* Hypertension~* Hypotension~Results show only those participants that had adjudicated and confirmed treatment-emergent composite cardiovascular AEs.
Time frame
Baseline, week 1, 2, and 8
Population
Safety analysis set. All randomised subjects who received at least one dose of the investigational product.

Source ClinicalTrials.gov

Trial

Title
Iron Isomaltoside/Ferric Derisomaltose vs Iron Sucrose for Treatment of Iron Deficiency Anemia in Non-Dialysis-Dependent Chronic Kidney Disease
NCT number
NCT02940860
Phases
PHASE3
Conditions
Iron Deficiency Anaemia, Iron Deficiency Anemia, Chronic Kidney Disease
Interventions
Iron isomaltoside/ferric derisomaltose, Iron sucrose
Lead sponsor
Pharmacosmos A/S
Results first posted
2020-03-06

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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