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85,013 comparisons from ClinicalTrials.gov. Counted 2026-11-10.
Most participants first33,758 with no events in either group come last1,101 to 1,120 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Prioritized Clinical Decision Support vs Usual Care: serious adverse events | 722 of 4,550 763 of 4,387 | -1.5 points -3.1 to 0.0 | 8,937 | NCT02451670 Reducing Cardiovascular Risk in Adults With Serious Mental Illness |
| NB32 vs Placebo: Percentage of Participants With a Confirmed Occurrence of Myocardial Infarction (Nonfatal or Fatal) | 55 of 4,455 57 of 4,450 | -0.0 points -0.5 to 0.4 | 8,905 | NCT01601704 Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study) |
| NB32 vs Placebo: Percentage of Participants With a Confirmed Occurrence of Cardiovascular Death (Including Fatal Myocardial Infarction, Fatal Stroke) | 17 of 4,455 34 of 4,450 | -0.4 points -0.7 to -0.1 | 8,905 | NCT01601704 Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study) |
| NB32 vs Placebo: Percentage of Participants With a Confirmed Occurrence of Major Adverse Cardiovascular Event (MACE) | 90 of 4,455 102 of 4,450 | -0.3 points -0.9 to 0.3 | 8,905 | NCT01601704 Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study) |
| NB32 vs Placebo: Percentage of Participants With a Confirmed Occurrence of Stroke (Nonfatal or Fatal) | 22 of 4,455 21 of 4,450 | 0.0 points -0.3 to 0.3 | 8,905 | NCT01601704 Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study) |
| NB32 vs Placebo: Percentage of Participants With a Confirmed Occurrence of Cardiovascular Death, Nonfatal Myocardial Infarction, Nonfatal Stroke, or Nonfatal Unstable Angina Requiring Hospitalization | 133 of 4,455 142 of 4,450 | -0.2 points -0.9 to 0.5 | 8,905 | NCT01601704 Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study) |
| NB32 vs Placebo: serious adverse events | 463 of 4,455 386 of 4,450 | 1.7 points 0.5 to 2.9 | 8,905 | NCT01601704 Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study) |
| LABA-LAMA-ICS vs LABA-LAMA: Number of Participants Hospitalised With Severe Exacerbation | 3,074 of 6,921 630 of 1,932 | 11.8 points 9.4 to 14.2 | 8,853 | NCT03724877 Effectiveness of Triple Therapy in COPD |
| LABA-LAMA-ICS vs LABA-LAMA: Number of Participants Hospitalised With Community-acquired Pneumonia (Serious Pneumonia) | 3,099 of 6,921 634 of 1,932 | 12.0 points 9.5 to 14.3 | 8,853 | NCT03724877 Effectiveness of Triple Therapy in COPD |
| LABA-LAMA-ICS vs LABA-LAMA: Number of Participants Hospitalised With Moderate Exacerbation | 2,487 of 6,921 542 of 1,932 | 7.9 points 5.5 to 10.1 | 8,853 | NCT03724877 Effectiveness of Triple Therapy in COPD |
| Brief Clinician Education vs Clinical Decision Support Nudges and Brief Clinician Education: Urine Testing for Non-specific Reasons | 1,127 of 4,535 1,032 of 4,264 | 0.6 points -1.2 to 2.4 | 8,799 | NCT04289753 Behavioral Economics Applications to Geriatrics Leveraging EHRs R33 Trial |
| Cangrelor Arm vs Clopidogrel Arm: Incidence of Thrombolysis in Myocardial Infarction (TIMI) Major Bleeding | 19 of 4,374 14 of 4,365 | 0.1 points -0.2 to 0.4 | 8,739 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Cangrelor Arm vs Clopidogrel Arm: Incidence of GUSTO Severe / Life-threatening Bleeding | 10 of 4,374 11 of 4,365 | -0.0 points -0.2 to 0.2 | 8,739 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Cangrelor Arm vs Clopidogrel Arm: Incidence of ACUITY Major Bleeding | 151 of 4,374 120 of 4,365 | 0.7 points -0.0 to 1.4 | 8,739 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Cangrelor Arm vs Clopidogrel Arm: Incidence of ACUITY Major Bleeding (Without Hematoma >/= 5 cm) | 78 of 4,374 65 of 4,365 | 0.3 points -0.2 to 0.8 | 8,739 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Cangrelor Arm vs Clopidogrel Arm: serious adverse events | 125 of 4,374 127 of 4,365 | -0.1 points -0.8 to 0.7 | 8,739 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| E-ZES vs C-SES: To Compare Overall Definite or Probable Stent Thrombosis Rate of the Endeavor® Zotarolimus Eluting Coronary Stent System Versus the Cypher® Sirolimus-eluting Coronary Stent in a Patient Population Requiring Stent Implantation | 61 of 4,357 75 of 4,352 | -0.3 points -0.9 to 0.2 | 8,709 | NCT00476957 Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) |
| E-ZES vs C-SES: serious adverse events | 579 of 4,357 507 of 4,352 | 1.6 points 0.3 to 3.0 | 8,709 | NCT00476957 Randomized Study Comparing Endeavor With Cypher Stents (PROTECT) |
| Rotarix Group vs Placebo Group: serious adverse events | 10 of 4,359 11 of 4,328 | -0.0 points -0.3 to 0.2 | 8,687 | NCT00329745 Year 3 Extension for Efficacy Follow-up in Subjects Vaccinated in Studies Rota-028, 029 or 030 (NCT00197210) |
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: Number of Participants With Unsolicited Adverse Events | 1,345 of 4,328 1,355 of 4,344 | -0.1 points -2.1 to 1.8 | 8,672 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=56
{
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{
"id": "NCT02451670-sae",
"title": "Prioritized Clinical Decision Support vs Usual Care: serious adverse events",
"summary": "722 of 4550 against 763 of 4387; risk difference -1.5 points, 95% interval -3.1 to 0.0; NCT02451670, Reducing Cardiovascular Risk in Adults With Serious Mental Illness",
"record": "/library/comparisons/NCT02451670-sae",
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"trial_title": "Reducing Cardiovascular Risk in Adults With Serious Mental Illness"
},
{
"id": "NCT01601704-3292f305",
"title": "NB32 vs Placebo: Percentage of Participants With a Confirmed Occurrence of Myocardial Infarction (Nonfatal or Fatal)",
"summary": "55 of 4455 against 57 of 4450; risk difference -0.0 points, 95% interval -0.5 to 0.4; NCT01601704, Cardiovascular Outcomes Study of Naltrexone SR/Bupropion SR in Overweight and Obese Subjects With Cardiovascular Risk Factors (The Light Study)",
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"terms": [
{
"source": "ClinicalTrials.gov's posted results, through CTTI's AACT",
"license": "ClinicalTrials.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",
"notice": "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.",
"short": "Freely available. Acknowledgement requested"
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{
"source": "ClinicalTrials.gov",
"license": "none stated",
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}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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