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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 last1,121 to 1,140 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: serious adverse events | 145 of 4,328 132 of 4,344 | 0.3 points -0.4 to 1.1 | 8,672 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
| Standard Implementation Strategy Period vs Enhanced Contact Investigation Intervention Period: TB Yield (Diagnosis and Treatment Initiation) | 36 of 2,874 187 of 5,761 | -2.0 points -2.6 to -1.4 | 8,635 | NCT05640648 Human-centered Design and Communities of Practice to Improve Home-based Tuberculosis Contact Investigation in Uganda |
| Standard Implementation Strategy Period vs Enhanced Contact Investigation Intervention Period: TB Yield (All Contacts) | 45 of 2,874 201 of 5,761 | -1.9 points -2.6 to -1.2 | 8,635 | NCT05640648 Human-centered Design and Communities of Practice to Improve Home-based Tuberculosis Contact Investigation in Uganda |
| Standard Implementation Strategy Period vs Enhanced Contact Investigation Intervention Period: Number of Contacts Diagnosed With Active TB | 45 of 2,874 201 of 5,761 | -1.9 points -2.6 to -1.2 | 8,635 | NCT05640648 Human-centered Design and Communities of Practice to Improve Home-based Tuberculosis Contact Investigation in Uganda |
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: Number of Participants With Local Injection Site Reactogenicity | 1,621 of 4,307 1,745 of 4,319 | -2.8 points -4.8 to -0.7 | 8,626 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: Number of Participants With Systemic Reactogenicity | 1,077 of 4,306 1,106 of 4,318 | -0.6 points -2.4 to 1.2 | 8,624 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: Number of Participants With rtPCR-confirmed Influenza-Like Illness | 96 of 4,303 138 of 4,301 | -1.0 points -1.7 to -0.3 | 8,604 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: Number of Participants With rtPCR-confirmed CDC-defined Influenza-Like Illness | 54 of 4,303 83 of 4,301 | -0.7 points -1.2 to -0.1 | 8,604 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: Number of Participants With Culture-confirmed Influenza-Like Illness | 58 of 4,303 101 of 4,301 | -1.0 points -1.6 to -0.4 | 8,604 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
| Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: Number of Participants With Culture-confirmed CDC-defined Influenza-Like Illness | 38 of 4,303 64 of 4,301 | -0.6 points -1.1 to -0.1 | 8,604 | NCT02285998 Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age |
| Intensive Control of SBP vs Standard Control of SBP: Number of Patients With All-cause Dementia | 149 of 4,278 176 of 4,285 | -0.6 points -1.4 to 0.2 | 8,563 | NCT01206062 Systolic Blood Pressure Intervention Trial |
| Intervention Email vs Control: Impact on Evaluation Rate | 3,387 of 4,269 3,337 of 4,218 | 0.2 points -1.5 to 2.0 | 8,487 | NCT02476578 Low Indexes of Metabolism - Information to Teams (LIMIT) |
| Intervention Email vs Control: Death From Any Cause | 285 of 4,269 245 of 4,218 | 0.9 points -0.2 to 1.9 | 8,487 | NCT02476578 Low Indexes of Metabolism - Information to Teams (LIMIT) |
| Intervention Email vs Control: deaths from any cause | 285 of 4,269 245 of 4,218 | 0.9 points -0.2 to 1.9 | 8,487 | NCT02476578 Low Indexes of Metabolism - Information to Teams (LIMIT) |
| Derivation Cohort vs Validation Cohort: deaths from any cause | 316 of 6,038 132 of 2,438 | -0.2 points -1.3 to 0.8 | 8,476 | NCT03491891 Factors Contribute to Very Late Stent Thrombosis After New Generation DES Implantation in China |
| LCZ696 vs Enalapril: serious adverse events | 1,937 of 4,203 2,142 of 4,229 | -4.6 points -6.7 to -2.4 | 8,432 | NCT01035255 This Study Will Evaluate the Efficacy and Safety of LCZ696 Compared to Enalapril on Morbidity and Mortality of Patients With Chronic Heart Failure |
| Intervention vs Control Group: deaths from any cause | 145 of 4,556 154 of 3,857 | -0.8 points -1.6 to -0.0 | 8,413 | NCT03044158 GeneXpert Performance Evaluation for Linkage to Tuberculosis Care |
| S-268019-b vs Placebo: Number of Participants With First Occurrence of SARS-CoV-2 RT-PCR-Positive Severe COVID-19 in the Initial Vaccination Period | 0 of 5,596 1 of 2,805 | -0.0 points -0.2 to 0.0 | 8,401 | NCT05212948 A Study of S-268019 for the Prevention of COVID-19 |
| S-268019-b vs Placebo: Number of Participants With First Occurrence of SARS-CoV-2 RT-PCR-Positive Symptomatic COVID-19 in the Initial Vaccination Period | 457 of 5,595 313 of 2,805 | -3.0 points -4.4 to -1.7 | 8,400 | NCT05212948 A Study of S-268019 for the Prevention of COVID-19 |
| LCZ696 vs Enalapril: Number of Patients With First Confirmed Renal Dysfunction | 94 of 4,187 108 of 4,212 | -0.3 points -1.0 to 0.3 | 8,399 | NCT01035255 This Study Will Evaluate the Efficacy and Safety of LCZ696 Compared to Enalapril on Morbidity and Mortality of Patients With Chronic Heart Failure |
Response
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{
"id": "NCT05640648-2a72ce86",
"title": "Standard Implementation Strategy Period vs Enhanced Contact Investigation Intervention Period: TB Yield (Diagnosis and Treatment Initiation)",
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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.
NCBI Gene
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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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