Comparison · NCT02322892-72dcc1f8
Thiamine vs Control Arm: Patients With Post-operative Complications
Calculated by ConductScience from the counts the trial posted to ClinicalTrials.gov.
2 sourcestrial-comparisons-2026-03-23-0.1.0
Cite this record
ConductScience Library. Thiamine vs Control Arm: Patients With Post-operative Complications. Trial comparisons, record NCT02322892-72dcc1f8. Release trial-comparisons-2026-03-23-0.1.0, 23 Mar 2026. https://conductscience.org/library/comparisons/NCT02322892-72dcc1f8
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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 | 0.516 | 0.348 | 0.68 | wilson | |
| Risk in group 2 | 0.485 | 0.325 | 0.648 | wilson | |
| Risk difference, group 1 minus group 2 | 0.0313 | -0.203 | 0.26 | newcombe hybrid score | |
| Risk ratio, group 1 over group 2 | 1.06 | 0.652 | 1.74 | log | |
| Odds ratio, group 1 over group 2 | 1.13 | 0.425 | 3.02 | log | |
| Number needed to treat, for one more participant with the outcome on Thiamine than on Control Arm | 32 | from the risk difference interval | the interval includes no difference |
Source ClinicalTrials.gov
Groups2
Group 2 names the comparator: control.
| Group | Title | Description | With the outcome | Analysed | ClinicalTrials.gov code |
|---|---|---|---|---|---|
| Group 1 | Thiamine | 200 mg thiamine in 50 mL normal saline solution~Thiamine: 200 mg thiamine in 50 mL normal saline once immediately before surgery and once immediately after (at arrival in the intensive care unit) | 16 | 31 | OG001 |
| Group 2 | Control Arm | 50 mL normal saline solution~Normal saline solution: 50 mL normal saline once immediately before surgery and once immediately after (at arrival in the intensive care unit) | 16 | 33 | OG000 |
Source ClinicalTrials.gov
Outcome
- Type
- SECONDARY
- Title
- Patients With Post-operative Complications
- Description
- Atrial fibrillation, delirium, renal failure, stroke, myocardial infarction, acute respiratory distress syndrome, infection
- Time frame
- Until hospital discharge, limit 60 days
- Population
Source ClinicalTrials.gov
Trial
- Title
- Thiamine as an Adjunctive Therapy in Cardiac Surgery
- NCT number
- NCT02322892
- Phases
- PHASE2
- Conditions
- Coronary Artery Bypass, Cardiac Surgical Procedures
- Interventions
- Thiamine, Normal saline solution
- Lead sponsor
- Beth Israel Deaconess Medical Center
- Results first posted
- 2017-03-30
- Results on ClinicalTrials.gov
- https://clinicaltrials.gov/study/NCT02322892?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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