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85,013 comparisons from ClinicalTrials.gov.
Most participants first33,758 with no events in either group come last3,701 to 3,720 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Rehospitalisation for Cardiac Reasons | 45 of 949 41 of 948 | 0.4 points -1.5 to 2.3 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Rehospitalisation for Non-cardiac Reasons | 19 of 949 11 of 948 | 0.8 points -0.3 to 2.1 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Serious Resuscitated Ventricular Fibrillation in Association With Invasive Procedures | 10 of 949 29 of 948 | -2.0 points -3.4 to -0.7 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Total Fatal Stroke | 7 of 949 4 of 948 | 0.3 points -0.4 to 1.1 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): deaths from any cause | 43 of 949 42 of 948 | 0.1 points -1.8 to 2.0 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With All-cause Mortality, Cardiogenic Shock, Congestive Heart Failure and Recurrent Myocardial Infarction Within 30 Days for FAS. | 116 of 949 135 of 948 | -2.0 points -5.1 to 1.0 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Cardiac Mortality | 31 of 949 32 of 948 | -0.1 points -1.8 to 1.5 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Minor Non-intracranial Bleeds | 206 of 949 191 of 948 | 1.6 points -2.1 to 5.2 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With All Cause Death and Shock and CHF | 100 of 949 123 of 948 | -2.4 points -5.3 to 0.5 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Total Non-disabling Stroke | 8 of 949 1 of 948 | 0.7 points 0.1 to 1.6 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| Tenecteplase (Group A) vs Primary PCI (Group B): serious adverse events | 146 of 949 164 of 948 | -1.9 points -5.2 to 1.4 | 1,897 | NCT00623623 STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction |
| M-M-R II ® vs Placebo: Risk of SARS-CoV-2 Infection up to 150 Days After Trial Intervention | 100 of 945 98 of 951 | 0.3 points -2.5 to 3.0 | 1,896 | NCT04333732 CROWN CORONATION: COVID-19 Research Outcomes Worldwide Network for CORONAvirus prevenTION |
| Dapivirine Vaginal Ring vs Placebo Vaginal Ring: The Incidence of Curable STIs | 682 of 1,271 315 of 624 | 3.2 points -1.6 to 7.9 | 1,895 | NCT01539226 Safety and Efficacy Trial of a Dapivirine Vaginal Matrix Ring in Healthy HIV-Negative Women |
| Placebo + IIV vs MEDI7510 + IIV: Number of Participants With Any Solicited Symptoms | 558 of 948 606 of 946 | -5.2 points -9.6 to -0.8 | 1,894 | NCT02508194 A Study to Evaluate the Efficacy of MEDI7510 in Older Adults |
| Placebo + IIV vs MEDI7510 + IIV: Number of Participants With Treatment-Emergent Adverse Events | 141 of 948 146 of 946 | -0.6 points -3.8 to 2.7 | 1,894 | NCT02508194 A Study to Evaluate the Efficacy of MEDI7510 in Older Adults |
| Placebo + IIV vs MEDI7510+IIV: deaths from any cause | 5 of 948 3 of 946 | 0.2 points -0.5 to 0.9 | 1,894 | NCT02508194 A Study to Evaluate the Efficacy of MEDI7510 in Older Adults |
| Placebo + IIV vs MEDI7510+IIV: serious adverse events | 57 of 948 64 of 946 | -0.8 points -3.0 to 1.5 | 1,894 | NCT02508194 A Study to Evaluate the Efficacy of MEDI7510 in Older Adults |
| Fluzone HD + mRNA-1345 Followed by Placebo vs Fluzone HD + Placebo Followed by mRNA-1345: Number of Participants With Unsolicited AEs Up to 21 Days After Day 22 Injection | 60 of 947 71 of 946 | -1.2 points -3.5 to 1.1 | 1,893 | NCT06060457 A Study to Evaluate the Safety and Immune Response of mRNA-1345, a Vaccine Targeting Respiratory Syncytial Virus (RSV), When Co-administered With a Fluzone HD, in Adults ≥65 Years of Age |
| Fluzone HD + mRNA-1345 Followed by Placebo vs Fluzone HD + Placebo Followed by mRNA-1345: Number of Participants With Unsolicited Adverse Events (AEs) Up to 21 Days After Day 1 Injection | 72 of 947 72 of 946 | -0.0 points -2.4 to 2.4 | 1,893 | NCT06060457 A Study to Evaluate the Safety and Immune Response of mRNA-1345, a Vaccine Targeting Respiratory Syncytial Virus (RSV), When Co-administered With a Fluzone HD, in Adults ≥65 Years of Age |
| Fluzone HD + mRNA-1345 Followed by Placebo vs Fluzone HD + Placebo Followed by mRNA-1345: serious adverse events | 23 of 947 33 of 946 | -1.1 points -2.6 to 0.5 | 1,893 | NCT06060457 A Study to Evaluate the Safety and Immune Response of mRNA-1345, a Vaccine Targeting Respiratory Syncytial Virus (RSV), When Co-administered With a Fluzone HD, in Adults ≥65 Years of Age |
Code
curl "https://conductscience.org/api/comparisons/v1?page=186"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=186
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00623623-b9ce0959",
"title": "Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Rehospitalisation for Cardiac Reasons",
"summary": "45 of 949 against 41 of 948; risk difference 0.4 points, 95% interval -1.5 to 2.3; NCT00623623, STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction",
"record": "/library/comparisons/NCT00623623-b9ce0959",
"nct_id": "NCT00623623",
"kind": "outcome",
"participants": 1897,
"risk_difference": {
"value": 0.004169389941888639,
"lower": -0.014830286578155369,
"upper": 0.02325145009135344
},
"group_1": "45 of 949",
"group_2": "41 of 948",
"difference": "0.4 points",
"interval": "-1.5 to 2.3",
"trial_title": "STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction"
},
{
"id": "NCT00623623-c787ae85",
"title": "Tenecteplase (Group A) vs Primary PCI (Group B): Number of Patients With Rehospitalisation for Non-cardiac Reasons",
"summary": "19 of 949 against 11 of 948; risk difference 0.8 points, 95% interval -0.3 to 2.1; NCT00623623, STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction",
"record": "/library/comparisons/NCT00623623-c787ae85",
"nct_id": "NCT00623623",
"kind": "outcome",
"participants": 1897,
"risk_difference": {
"value": 0.008417699288169201,
"lower": -0.0031297120397074333,
"upper": 0.020581111517223874
},
"group_1": "19 of 949",
"group_2": "11 of 948",
"difference": "0.8 points",
"interval": "-0.3 to 2.1",
"trial_title": "STREAM-Strategic Reperfusion (With Tenecteplase and Antithrombotic Treatment) Early After Myocardial Infarction"
}
],
"no_events": 33758,
"columns": [
{
"key": "title",
"label": "Comparison"
},
{
"key": "group_1",
"label": "With the outcome",
"under": "group_2"
},
{
"key": "difference",
"label": "Risk difference, 95% interval",
"under": "interval"
},
{
"key": "participants",
"label": "Participants"
},
{
"key": "nct_id",
"label": "Trial",
"under": "trial_title"
}
],
"order": "Most participants first",
"kinds": {
"all": 85013,
"outcome": 33568,
"serious-adverse-events": 31897,
"deaths": 19548
}
},
"release": "trial-comparisons-2026-03-23-0.1.0",
"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"
},
{
"source": "ClinicalTrials.gov",
"license": "none stated",
"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": "No license stated"
}
],
"next": "/api/comparisons/v1?page=187",
"request_id": "FMhRqWY6vF8zWHRE"
}Ask about these results. The first 10 go in the prompt.
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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Every answer on this page is also JSON, under /api/comparisons/v1. No key.
GET https://conductscience.org/api/comparisons/v1?q=placebo%20heart%20failure&kind=outcome
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