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Comparison · NCT03715790-140cdf8f

Referred Subjects vs Not Referred Subjects: Percentage of Post-Acute MI Patients Who Are Referred for Sudden Cardiac Death Risk Stratification > Risk (SCD) Stratification and Management

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. Referred Subjects vs Not Referred Subjects: Percentage of Post-Acute MI Patients Who Are Referred for Sudden Cardiac Death Risk Stratification > Risk (SCD) Stratification and Management. Trial comparisons, record NCT03715790-140cdf8f. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03715790-140cdf8f

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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 10.2020.180.226wilson
Risk in group 20.7980.7740.82wilson
Risk difference, group 1 minus group 2-0.597-0.628-0.563newcombe hybrid score
Risk ratio, group 1 over group 20.2530.2250.284log
Odds ratio, group 1 over group 20.06380.05220.0781log
Number needed to treat, for one fewer participant with the outcome on Referred Subjects than on Not Referred Subjects1.681.591.78from 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 1Referred SubjectsSubjects who were referred for SCA risk stratification2361,170OG000
Group 2Not Referred SubjectsSubjects who were not referred for SCA risk stratification9341,170OG001

Outcome

Type
PRIMARY
Title
Percentage of Post-Acute MI Patients Who Are Referred for Sudden Cardiac Death Risk Stratification > Risk (SCD) Stratification and Management
Description
The numerator for this endpoint will be defined as the number of patients who met the clinician's determination to refer the subject for SCD risk stratification and management at any of the three follow-up visits. The denominator for this endpoint is the number of patients who completed a 3-month follow-up visit. While the participant study flow is composed of referred and not referred groups, these groups are simply the results of the referral process in the single arm of enrolled patients. Thus the analysis of the endpoints is conducted within this one arm.~No hypotheses were tested for this endpoint.
Time frame
3-months post-MI to 12-months post-MI
Population
Enrolled subjects who were evaluated at 3-month follow up to determine if they met referral criteria or did not meet referral criteria.

Source ClinicalTrials.gov

Trial

Title
Improve SCA Bridge Study
NCT number
NCT03715790
Phases
Conditions
Sudden Cardiac Arrest, Acute Myocardial Infarction
Interventions
EP referred group, Non-Referred group
Lead sponsor
Medtronic Cardiac Rhythm and Heart Failure
Results first posted
2024-01-16

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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