Comparison · NCT02100722-3ad7aa32
FFR Guided PCI vs CABG: Number of Participants Experiencing Death, MI, or Stroke
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 Experiencing Death, MI, or Stroke. Trial comparisons, record NCT02100722-3ad7aa32. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02100722-3ad7aa32
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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 | 0.0727 | 0.0562 | 0.0934 | wilson | |
| Risk in group 2 | 0.0525 | 0.0386 | 0.071 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0202 | -0.00454 | 0.0451 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.38 | 0.93 | 2.06 | log | |
| Odds ratio, group 1 over group 2 | 1.41 | 0.926 | 2.16 | log | |
| Number needed to treat, for one more participant with the outcome on FFR Guided PCI than on CABG | 49.6 | from the risk difference interval | the interval includes no difference |
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. | 55 | 757 | OG000 |
| Group 2 | CABG | CABG performed per clinical routine (both off-pump and on-pump surgery acceptable). | 39 | 743 | OG001 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Number of Participants Experiencing Death, MI, or Stroke
- Description
- Subjects who died or are lost to follow up before this time were censored at their last recorded activity.
- Time frame
- 1 year
- 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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