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Comparison · NCT00187278-a2c29421

RV Pacing vs Biventricular Pacing: Adverse Events Related to Left Ventricular Lead

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. RV Pacing vs Biventricular Pacing: Adverse Events Related to Left Ventricular Lead. Trial comparisons, record NCT00187278-a2c29421. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT00187278-a2c29421

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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 10.00110.0001940.00621wilson
Risk in group 20.04210.03080.0573wilson
Risk difference, group 1 minus group 2-0.041-0.0562-0.0286newcombe hybrid score
Risk ratio, group 1 over group 20.02610.00360.19log
Odds ratio, group 1 over group 20.02510.003430.183log
Number needed to treat, for one fewer participant with the outcome on RV Pacing than on Biventricular Pacing24.417.834.9from 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 1RV PacingStandard Pacemaker implant1908OG000
Group 2Biventricular PacingBiventricular Pacemaker implant38902OG001

Outcome

Type
SECONDARY
Title
Adverse Events Related to Left Ventricular Lead
Description
Only serious adverse events related to the left ventricular lead are included.
Time frame
Study Duration (5.7 years mean follow-up)
Population

Source ClinicalTrials.gov

Trial

Title
Biopace Study: Biventricular Pacing for Atrioventricular Block to Prevent Cardiac Desynchronization
NCT number
NCT00187278
Phases
NA
Conditions
Atrioventricular Block, Ventricular Dysfunction
Interventions
Biventricular Pacing, RV Pacing
Lead sponsor
Abbott Medical Devices
Results first posted
2021-01-25

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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