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Comparison · NCT01756846-1b14404c

HEART Care vs Usual Care: MACE (Major Adverse Cardiac 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. HEART Care vs Usual Care: MACE (Major Adverse Cardiac Events). Trial comparisons, record NCT01756846-1b14404c. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT01756846-1b14404c

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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 10.1890.1720.208wilson
Risk in group 20.2220.2030.241wilson
Risk difference, group 1 minus group 2-0.0322-0.0584-0.00599newcombe hybrid score
Risk ratio, group 1 over group 20.8550.7520.971log
Odds ratio, group 1 over group 20.8210.6990.964log
Number needed to treat, for one fewer participant with the outcome on HEART Care than on Usual Care3117.1167from the risk difference interval

Groups2

Group 2 names the comparator: usual care.

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1HEART CareHEART care: usual care, complemented by calculation of the HEART score and following the recommended policy.3451,821OG001
Group 2Usual Care
usual care was defined as daily practice of the cardiologist or attending emergency doctor, in order to diagnose a patient with chest pain. In this period attending doctors assess the risk of a patient with chest pain, based on his/hers experience and various criteria (for example described in European Society of Cardiology Guidelines for the management of acute coronary syndromes in patients presenting without persistent ST-segment elevation, without a formal risk score).
4051,827OG000

Outcome

Type
PRIMARY
Title
MACE (Major Adverse Cardiac Events)
Description
occurrence of major adverse cardiac events (MACE, i.e. acute myocardial infarction (AMI), Percutaneous Coronary Intervention (PCI), Coronary Artery Bypass Grafting (CABG) or death) within 6 weeks after presentation
Time frame
6 weeks
Population

Source ClinicalTrials.gov

Trial

Title
Impact on Management of the HEART Risk Score in Chest Pain Patients
NCT number
NCT01756846
Phases
NA
Conditions
Chest Pain
Interventions
usual care, use of HEART risk score
Lead sponsor
UMC Utrecht
Results first posted
2019-01-25

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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