Comparison · NCT02100722-9d1a7a3e
FFR Guided PCI vs CABG: Number of Participants Requiring Rehospitalization Within 30 Days
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. FFR Guided PCI vs CABG: Number of Participants Requiring Rehospitalization Within 30 Days. Trial comparisons, record NCT02100722-9d1a7a3e. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02100722-9d1a7a3e
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Measures6
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
| Measure | Value | 95% interval, lower | 95% interval, upper | Method | Note |
|---|---|---|---|---|---|
| Risk in group 1 | 0.0555 | 0.0413 | 0.0741 | wilson | |
| Risk in group 2 | 0.102 | 0.0825 | 0.126 | wilson | |
| Risk difference, group 1 minus group 2 | -0.0468 | -0.0746 | -0.0196 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 0.542 | 0.377 | 0.78 | log | |
| Odds ratio, group 1 over group 2 | 0.516 | 0.349 | 0.762 | log | |
| Number needed to treat, for one fewer participant with the outcome on FFR Guided PCI than on CABG | 21.4 | 13.4 | 51 | from the risk difference interval |
Source ClinicalTrials.gov
Groups2
Neither group, or both, names a comparator, so the groups keep ClinicalTrials.gov's order.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | FFR Guided PCI | Patients undergoing PCI with measured FFR ≤0.80 have PCI performed with Medtronic Resolute Integrity (or Onyx) drug-eluting stent. | 42 | 757 | OG000 |
| Group 2 | CABG | CABG performed per clinical routine (both off-pump and on-pump surgery acceptable). | 76 | 743 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants Requiring Rehospitalization Within 30 Days
- Description
- Time frame
- 30 days
- Population
Source ClinicalTrials.gov
Trial
- Title
- A Comparison of Fractional Flow Reserve-Guided Percutaneous Coronary Intervention and Coronary Artery Bypass Graft Surgery in Patients With Multivessel Coronary Artery Disease
- NCT number
- NCT02100722
- Phases
- NA
- Conditions
- Coronary Disease, Coronary Stenosis
- Interventions
- FFR guided PCI, CABG, Resolute Integrity Stent, Resolute Onyx Stent
- Lead sponsor
- Stanford University
- Results first posted
- 2022-01-20
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02100722?tab=results
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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