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85,013 comparisons from ClinicalTrials.gov. Counted 2026-11-10.

85,013 comparisons

Most participants first33,758 with no events in either group come last1,161 to 1,180 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
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

8,179NCT01492361

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 events1,252 of 4,089

1,254 of 4,090

-0.0 points

-2.0 to 2.0

8,179NCT01492361

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 Causes616 of 4,089

678 of 4,075

-1.6 points

-3.2 to 0.0

8,164NCT00097669

VITATOPS: A Study of VITAmins TO Prevent Stroke

Herpes Simplex Virus Group vs Havrix Group: serious adverse events171 of 4,488

132 of 3,662

0.2 points

-0.6 to 1.0

8,150NCT00057330

HerpeVac Trial for Young Women

Dutasteride 0.5 mg vs Placebo: Number of Participants With Post-biopsy Macroscopic Hematospermia53 of 4,049

78 of 4,073

-0.6 points

-1.2 to -0.1

8,122NCT00056407

"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 Hematuria127 of 4,049

168 of 4,073

-1.0 points

-1.8 to -0.2

8,122NCT00056407

"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 Months116 of 4,421

123 of 3,695

-0.7 points

-1.5 to 0.0

8,116NCT03044158

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 Season5 of 4,038

21 of 4,019

-0.4 points

-0.7 to -0.2

8,057NCT05437510

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 Season11 of 4,038

64 of 4,019

-1.3 points

-1.8 to -0.9

8,057NCT05437510

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 events77 of 4,008

88 of 4,045

-0.3 points

-0.9 to 0.4

8,053NCT00463866

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 Vaccination54 of 4,261

47 of 3,788

0.0 points

-0.5 to 0.5

8,049NCT02378753

STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola)

rVSVΔG-ZEBOV (Immediate Vaccination) vs rVSVΔG-ZEBOV (Deferred Vaccination): Suspected, Probable or Laboratory-confirmed Ebola27 of 4,261

17 of 3,788

0.2 points

-0.1 to 0.5

8,049NCT02378753

STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola)

rVSVΔG-ZEBOV (Immediate Vaccination) vs rVSVΔG-ZEBOV (Deferred Vaccination): deaths from any cause8 of 4,261

11 of 3,788

-0.1 points

-0.3 to 0.1

8,049NCT02378753

STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola)

rVSVΔG-ZEBOV (Immediate Vaccination) vs rVSVΔG-ZEBOV (Deferred Vaccination): serious adverse events54 of 4,261

47 of 3,788

0.0 points

-0.5 to 0.5

8,049NCT02378753

STRIVE (Sierra Leone Trial to Introduce a Vaccine Against Ebola)

Evaluation Period vs Control Period: Antiretroviral Therapy (ART) Receipt3,508 of 3,786

4,106 of 4,259

-3.8 points

-4.8 to -2.8

8,045NCT02907944

Working With HIV Clinics to Adopt Addiction Treatments Using Implementation Facilitation

Intervention Period vs Control Period: Antiretroviral Therapy (ART) Receipt3,547 of 3,780

4,106 of 4,259

-2.6 points

-3.5 to -1.6

8,039NCT02907944

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 Referral599 of 6,294

0 of 1,744

9.5 points

8.8 to 10.3

8,038NCT03793972

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 cause1 of 6,294

0 of 1,744

0.0 points

-0.2 to 0.1

8,038NCT03793972

Triaging and Referring in Adjacent General and Emergency Departments

Triage With Referral to Primary Care vs Triage Without Referral to Primary Care: serious adverse events1 of 6,294

0 of 1,744

0.0 points

-0.2 to 0.1

8,038NCT03793972

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

8,034NCT05437510

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

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Words from a trial's title, conditions or interventions, its outcome or its groups, or an NCT number.

An outcome counted in participants, the serious adverse events, or the deaths from any cause.

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Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=59

{
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      {
        "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",
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        "difference": "-4.8 points",
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        "trial_title": "A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High-Risk Patients With Hypertriglyceridemia and on Statin"
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      {
        "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",
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        "group_1": "1,252 of 4,089",
        "group_2": "1,254 of 4,090",
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      "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.",
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      "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.",
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trial-comparisons-2026-03-23-0.1.0Next page

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone 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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