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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 last1,121 to 1,140 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: serious adverse events145 of 4,328

132 of 4,344

0.3 points

-0.4 to 1.1

8,672NCT02285998

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

8,635NCT05640648

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

8,635NCT05640648

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 TB45 of 2,874

201 of 5,761

-1.9 points

-2.6 to -1.2

8,635NCT05640648

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 Reactogenicity1,621 of 4,307

1,745 of 4,319

-2.8 points

-4.8 to -0.7

8,626NCT02285998

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 Reactogenicity1,077 of 4,306

1,106 of 4,318

-0.6 points

-2.4 to 1.2

8,624NCT02285998

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 Illness96 of 4,303

138 of 4,301

-1.0 points

-1.7 to -0.3

8,604NCT02285998

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 Illness54 of 4,303

83 of 4,301

-0.7 points

-1.2 to -0.1

8,604NCT02285998

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 Illness58 of 4,303

101 of 4,301

-1.0 points

-1.6 to -0.4

8,604NCT02285998

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 Illness38 of 4,303

64 of 4,301

-0.6 points

-1.1 to -0.1

8,604NCT02285998

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 Dementia149 of 4,278

176 of 4,285

-0.6 points

-1.4 to 0.2

8,563NCT01206062

Systolic Blood Pressure Intervention Trial

Intervention Email vs Control: Impact on Evaluation Rate3,387 of 4,269

3,337 of 4,218

0.2 points

-1.5 to 2.0

8,487NCT02476578

Low Indexes of Metabolism - Information to Teams (LIMIT)

Intervention Email vs Control: Death From Any Cause285 of 4,269

245 of 4,218

0.9 points

-0.2 to 1.9

8,487NCT02476578

Low Indexes of Metabolism - Information to Teams (LIMIT)

Intervention Email vs Control: deaths from any cause285 of 4,269

245 of 4,218

0.9 points

-0.2 to 1.9

8,487NCT02476578

Low Indexes of Metabolism - Information to Teams (LIMIT)

Derivation Cohort vs Validation Cohort: deaths from any cause316 of 6,038

132 of 2,438

-0.2 points

-1.3 to 0.8

8,476NCT03491891

Factors Contribute to Very Late Stent Thrombosis After New Generation DES Implantation in China

LCZ696 vs Enalapril: serious adverse events1,937 of 4,203

2,142 of 4,229

-4.6 points

-6.7 to -2.4

8,432NCT01035255

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 cause145 of 4,556

154 of 3,857

-0.8 points

-1.6 to -0.0

8,413NCT03044158

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 Period0 of 5,596

1 of 2,805

-0.0 points

-0.2 to 0.0

8,401NCT05212948

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 Period457 of 5,595

313 of 2,805

-3.0 points

-4.4 to -1.7

8,400NCT05212948

A Study of S-268019 for the Prevention of COVID-19

LCZ696 vs Enalapril: Number of Patients With First Confirmed Renal Dysfunction94 of 4,187

108 of 4,212

-0.3 points

-1.0 to 0.3

8,399NCT01035255

This Study Will Evaluate the Efficacy and Safety of LCZ696 Compared to Enalapril on Morbidity and Mortality of Patients With Chronic Heart Failure

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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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The first 2 of this page's 20 results. GET /api/comparisons/v1?page=57

{
  "data": {
    "total": 85013,
    "results": [
      {
        "id": "NCT02285998-sae",
        "title": "Flublok Quadrivalent Influenza Vaccine vs Inactivated Influenza Vaccine: serious adverse events",
        "summary": "145 of 4328 against 132 of 4344; risk difference 0.3 points, 95% interval -0.4 to 1.1; NCT02285998, Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age",
        "record": "/library/comparisons/NCT02285998-sae",
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        "group_2": "132 of 4,344",
        "difference": "0.3 points",
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        "trial_title": "Protective Efficacy of Flublok® Quadrivalent Versus Licensed Inactivated Influenza Vaccine in Adults ≥50 Years of Age"
      },
      {
        "id": "NCT05640648-2a72ce86",
        "title": "Standard Implementation Strategy Period vs Enhanced Contact Investigation Intervention Period: TB Yield (Diagnosis and Treatment Initiation)",
        "summary": "36 of 2874 against 187 of 5761; risk difference -2.0 points, 95% interval -2.6 to -1.4; NCT05640648, Human-centered Design and Communities of Practice to Improve Home-based Tuberculosis Contact Investigation in Uganda",
        "record": "/library/comparisons/NCT05640648-2a72ce86",
        "nct_id": "NCT05640648",
        "kind": "outcome",
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        "group_1": "36 of 2,874",
        "group_2": "187 of 5,761",
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        "interval": "-2.6 to -1.4",
        "trial_title": "Human-centered Design and Communities of Practice to Improve Home-based Tuberculosis Contact Investigation in Uganda"
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      "serious-adverse-events": 31897,
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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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      "source": "ClinicalTrials.gov",
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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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