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Comparison · NCT00093015-e64fcaab

Darbepoetin Alfa vs Placebo: Time to Hospitalization Due to Acute Myocardial Ischemia

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. Darbepoetin Alfa vs Placebo: Time to Hospitalization Due to Acute Myocardial Ischemia. Trial comparisons, record NCT00093015-e64fcaab. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00093015-e64fcaab

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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 10.02040.01510.0275wilson
Risk in group 20.02420.01830.0318wilson
Risk difference, group 1 minus group 2-0.00381-0.01310.00543newcombe hybrid score
Risk ratio, group 1 over group 20.8430.5591.27log
Odds ratio, group 1 over group 20.8390.5521.28log
Number needed to treat, for one fewer participant with the outcome on Darbepoetin Alfa than on Placebo263from the risk difference intervalthe interval includes no difference

Groups2

Group 2 names the comparator: placebo.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Darbepoetin Alfa
Subcutaneous darbepoetin alfa at a starting dose of 75 mcg/kg once every 2 weeks, titrated to maintain a hemoglobin concentration of 13.0 g/dL. Dosing was switched to once monthly when two consecutive hemoglobin concentrations between 12.0 and 13.5 g/dL were observed.
412,012OG001
Group 2Placebo
Subcutaneous placebo when hemoglobin concentration was ≥ 9.0 g/dL. Received subcutaneous rescue therapy (once monthly) with darbepoetin alfa in a blinded fashion if the hemoglobin concentration was \<9.0 g/dL until the hemoglobin concentration was ≥ 9.0 g/dL.
492,026OG000

Outcome

Type
SECONDARY
Title
Time to Hospitalization Due to Acute Myocardial Ischemia
Description
Time from randomization to hospitalization due to acute myocardial ischemia. Kaplan-Meier estimate of the median time was not estimable due to low proportion of participants experiencing at least one events, therefore participants experiencing at least one event were summarized.
Time frame
Until a primary cardiovascular event (death, myocardial ischemia, congestive heart failure, myocardial infarction or cerebrovascular accident) occurred or 28 March 2009, whichever occurred first
Population
The analysis followed intent-to-treat principles. Subjects were analyzed as randomized using all available follow-up information.

Source ClinicalTrials.gov

Trial

Title
Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT)
NCT number
NCT00093015
Phases
PHASE3
Conditions
Kidney Disease, Diabetes Mellitus, Anemia
Interventions
Placebo, darbepoetin alfa
Lead sponsor
Amgen
Results first posted
2010-09-02

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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