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One gene with its proteins, patents, drugs, trials, grants and papers.
85,013 comparisons from ClinicalTrials.gov. Counted 2026-11-10.
Most participants first33,758 with no events in either group come last1,161 to 1,180 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| AMR101 vs Placebo: Composite of CV Death, Nonfatal MI (Including Silent MI), Nonfatal Stroke, Coronary Revascularization, or Unstable Angina Determined to be Caused by Myocardial Ischemia by Invasive / Non-invasive Testing and Requiring Emergent Hospitalization. | 705 of 4,089 901 of 4,090 | -4.8 points -6.5 to -3.1 | 8,179 | NCT01492361 A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High-Risk Patients With Hypertriglyceridemia and on Statin |
| AMR101 vs Placebo: serious adverse events | 1,252 of 4,089 1,254 of 4,090 | -0.0 points -2.0 to 2.0 | 8,179 | NCT01492361 A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High-Risk Patients With Hypertriglyceridemia and on Statin |
| Active VITATOPS Tablet (Folic Acid 2mg, B6 25mg , B12 500ug) vs Placebo Tablet: Non-fatal Stroke, Non-fatal Myocardial Infarction or Death Due to Vascular Causes | 616 of 4,089 678 of 4,075 | -1.6 points -3.2 to 0.0 | 8,164 | NCT00097669 VITATOPS: A Study of VITAmins TO Prevent Stroke |
| Herpes Simplex Virus Group vs Havrix Group: serious adverse events | 171 of 4,488 132 of 3,662 | 0.2 points -0.6 to 1.0 | 8,150 | NCT00057330 HerpeVac Trial for Young Women |
| Dutasteride 0.5 mg vs Placebo: Number of Participants With Post-biopsy Macroscopic Hematospermia | 53 of 4,049 78 of 4,073 | -0.6 points -1.2 to -0.1 | 8,122 | NCT00056407 "REDUCE" - A Clinical Research Study To Reduce The Incidence Of Prostate Cancer In Men Who Are At Increased Risk |
| Dutasteride 0.5 mg vs Placebo: Number of Participants With Post-biopsy Macroscopic Hematuria | 127 of 4,049 168 of 4,073 | -1.0 points -1.8 to -0.2 | 8,122 | NCT00056407 "REDUCE" - A Clinical Research Study To Reduce The Incidence Of Prostate Cancer In Men Who Are At Increased Risk |
| Intervention vs Control Group: Number Who Died Within 6 Months | 116 of 4,421 123 of 3,695 | -0.7 points -1.5 to 0.0 | 8,116 | NCT03044158 GeneXpert Performance Evaluation for Linkage to Tuberculosis Care |
| Nirsevimab vs No Intervention: Number of Participants With Very Severe Respiratory Syncytial Virus Lower Respiratory Tract Infection Through the Respiratory Syncytial Virus Season | 5 of 4,038 21 of 4,019 | -0.4 points -0.7 to -0.2 | 8,057 | NCT05437510 Study of a Single Intramuscular Dose of Nirsevimab in the Prevention of Hospitalizations Due to Respiratory Syncytial Virus (RSV) Infection in Healthy Term and Preterm Infants During the First Year of Life |
| Nirsevimab vs No Intervention: Number of Participants With Respiratory Syncytial Virus (RSV) Lower Respiratory Tract Infection (LRTI) Hospitalization Through the Respiratory Syncytial Virus Season | 11 of 4,038 64 of 4,019 | -1.3 points -1.8 to -0.9 | 8,057 | NCT05437510 Study of a Single Intramuscular Dose of Nirsevimab in the Prevention of Hospitalizations Due to Respiratory Syncytial Virus (RSV) Infection in Healthy Term and Preterm Infants During the First Year of Life |
| Symbicort® SMART®) 1*2 vs Symbicort® SMART®) 2*2: serious adverse events | 77 of 4,008 88 of 4,045 | -0.3 points -0.9 to 0.4 | 8,053 | NCT00463866 Local Phase 4 Pan-European SMART Study |
| rVSVΔG-ZEBOV (Immediate Vaccination) vs rVSVΔG-ZEBOV (Deferred Vaccination): Number of Participants With Occurrence of Serious Adverse Events During the 6 Months Following the Vaccination | 54 of 4,261 47 of 3,788 | 0.0 points -0.5 to 0.5 | 8,049 | NCT02378753 STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola) |
| rVSVΔG-ZEBOV (Immediate Vaccination) vs rVSVΔG-ZEBOV (Deferred Vaccination): Suspected, Probable or Laboratory-confirmed Ebola | 27 of 4,261 17 of 3,788 | 0.2 points -0.1 to 0.5 | 8,049 | NCT02378753 STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola) |
| rVSVΔG-ZEBOV (Immediate Vaccination) vs rVSVΔG-ZEBOV (Deferred Vaccination): deaths from any cause | 8 of 4,261 11 of 3,788 | -0.1 points -0.3 to 0.1 | 8,049 | NCT02378753 STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola) |
| rVSVΔG-ZEBOV (Immediate Vaccination) vs rVSVΔG-ZEBOV (Deferred Vaccination): serious adverse events | 54 of 4,261 47 of 3,788 | 0.0 points -0.5 to 0.5 | 8,049 | NCT02378753 STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola) |
| Evaluation Period vs Control Period: Antiretroviral Therapy (ART) Receipt | 3,508 of 3,786 4,106 of 4,259 | -3.8 points -4.8 to -2.8 | 8,045 | NCT02907944 Working With HIV Clinics to Adopt Addiction Treatments Using Implementation Facilitation |
| Intervention Period vs Control Period: Antiretroviral Therapy (ART) Receipt | 3,547 of 3,780 4,106 of 4,259 | -2.6 points -3.5 to -1.6 | 8,039 | NCT02907944 Working With HIV Clinics to Adopt Addiction Treatments Using Implementation Facilitation |
| Triage With Referral to Primary Care vs Triage Without Referral to Primary Care: The Proportion of Patients Presenting at the ED But Being Treated by the GPC After Referral | 599 of 6,294 0 of 1,744 | 9.5 points 8.8 to 10.3 | 8,038 | NCT03793972 Triaging and Referring in Adjacent General and Emergency Departments |
| Triage With Referral to Primary Care vs Triage Without Referral to Primary Care: deaths from any cause | 1 of 6,294 0 of 1,744 | 0.0 points -0.2 to 0.1 | 8,038 | NCT03793972 Triaging and Referring in Adjacent General and Emergency Departments |
| Triage With Referral to Primary Care vs Triage Without Referral to Primary Care: serious adverse events | 1 of 6,294 0 of 1,744 | 0.0 points -0.2 to 0.1 | 8,038 | NCT03793972 Triaging and Referring in Adjacent General and Emergency Departments |
| Nirsevimab vs No Intervention: Number of Participants With Immediate Treatment-Emergent Adverse Events (TEAEs) | 27 of 4,016 0 of 4,018 | 0.7 points 0.4 to 1.0 | 8,034 | NCT05437510 Study of a Single Intramuscular Dose of Nirsevimab in the Prevention of Hospitalizations Due to Respiratory Syncytial Virus (RSV) Infection in Healthy Term and Preterm Infants During the First Year of Life |
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=59
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT01492361-e80ebb8f",
"title": "AMR101 vs Placebo: Composite of CV Death, Nonfatal MI (Including Silent MI), Nonfatal Stroke, Coronary Revascularization, or Unstable Angina Determined to be Caused by Myocardial Ischemia by Invasive / Non-invasive Testing and Requiring Emergent Hospitalization.",
"summary": "705 of 4089 against 901 of 4090; risk difference -4.8 points, 95% interval -6.5 to -3.1; NCT01492361, A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High-Risk Patients With Hypertriglyceridemia and on Statin",
"record": "/library/comparisons/NCT01492361-e80ebb8f",
"nct_id": "NCT01492361",
"kind": "outcome",
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"risk_difference": {
"value": -0.04787960542955905,
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"upper": -0.030678485013301716
},
"group_1": "705 of 4,089",
"group_2": "901 of 4,090",
"difference": "-4.8 points",
"interval": "-6.5 to -3.1",
"trial_title": "A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High-Risk Patients With Hypertriglyceridemia and on Statin"
},
{
"id": "NCT01492361-sae",
"title": "AMR101 vs Placebo: serious adverse events",
"summary": "1252 of 4089 against 1254 of 4090; risk difference -0.0 points, 95% interval -2.0 to 2.0; NCT01492361, A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High-Risk Patients With Hypertriglyceridemia and on Statin",
"record": "/library/comparisons/NCT01492361-sae",
"nct_id": "NCT01492361",
"kind": "serious-adverse-events",
"participants": 8179,
"risk_difference": {
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"lower": -0.020389130477220033,
"upper": 0.019561407143183825
},
"group_1": "1,252 of 4,089",
"group_2": "1,254 of 4,090",
"difference": "-0.0 points",
"interval": "-2.0 to 2.0",
"trial_title": "A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High-Risk Patients With Hypertriglyceridemia and on Statin"
}
],
"no_events": 33758,
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"deaths": 19548
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"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"
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{
"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": "None stated"
}
],
"next": "/api/comparisons/v1?page=60",
"request_id": "tdCj1Y1jV4J3bvRi"
}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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