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Comparison · NCT03426124-a3622a5d

Retrospective vs Prospective: All-cause Mortality During First 12 Months Post-procedure.

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. Retrospective vs Prospective: All-cause Mortality During First 12 Months Post-procedure. Trial comparisons, record NCT03426124-a3622a5d. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT03426124-a3622a5d

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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 10.05050.03850.0659wilson
Risk in group 20.03070.01870.05wilson
Risk difference, group 1 minus group 20.0198-0.002950.0393newcombe hybrid score
Risk ratio, group 1 over group 21.640.9332.9log
Odds ratio, group 1 over group 21.680.9333.02log
Number needed to treat, for one more participant with the outcome on Retrospective than on Prospective50.6from the risk difference intervalthe interval includes no difference

Groups2

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

GroupTitleDescriptionWith the outcomeAnalysedClinicalTrials.gov code
Group 1Retrospective
Individuals with intermediate-high or high risk pulmonary embolism who were consecutively treated with the Ekosonic Endovascular System (EKOS) and thrombolytic drug between January 2014 and one year prior to site activation.~EkoSonic Endovascular System with thrombolytic: The device uses ultrasonic waves in combination with clot-dissolving thrombolytic drug to effectively dissolve clots.
50991OG000
Group 2Prospective
Individuals who are experiencing intermediate-high or high risk pulmonary embolism where the treating investigator has selected the EKOS device and thrombolytic drug. The duration of ultrasound and volume of thrombolytic drug are selected per physician discretion.~EkoSonic Endovascular System with thrombolytic: The device uses ultrasonic waves in combination with clot-dissolving thrombolytic drug to effectively dissolve clots.
15489OG001

Outcome

Type
PRIMARY
Title
All-cause Mortality During First 12 Months Post-procedure.
Description
Number of all-cause mortality that occurred from the start of procedure through 12 months post-procedure.
Time frame
Start of procedure through 12 months post-procedure.
Population
Retrospective data to be updated.

Source ClinicalTrials.gov

Trial

Title
An International Pulmonary Embolism Registry Using EKOS
NCT number
NCT03426124
Phases
Conditions
Pulmonary Embolism and Thrombosis
Interventions
EkoSonic Endovascular System with thrombolytic
Lead sponsor
Boston Scientific Corporation
Results first posted
2023-02-22

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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