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85,013 comparisons from ClinicalTrials.gov.

85,013 comparisons

Most participants first33,758 with no events in either group come last1,881 to 1,900 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
MACE Events Within 90 Days Subject Whose FFRCT Was >0.80 vs MACE Events Within 90 Days. Patients With at Least One FFRCT Value ≤ 0.80: Percentage of Major Adverse Coronary Events (MACE) at 90 Days0 of 1,592

19 of 3,145

-0.6 points

-0.9 to -0.3

4,737NCT02499679

Assessing Diagnostic Value of Non-invasive FFRCT in Coronary Care

Dapa 10mg vs Placebo: deaths from any cause286 of 2,368

333 of 2,368

-2.0 points

-3.9 to -0.1

4,736NCT03036124

Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure

Dapa 10mg vs Placebo: serious adverse events895 of 2,368

994 of 2,368

-4.2 points

-7.0 to -1.4

4,736NCT03036124

Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure

BP Trial: Intensive Control vs BP Trial: Standard Control: First Occurrence of Major Cardiovascular Event (MCE) in the Blood Pressure Trial.208 of 2,363

237 of 2,371

-1.2 points

-2.9 to 0.5

4,734NCT00000620

Action to Control Cardiovascular Risk in Diabetes (ACCORD)

BP Trial: Intensive Control vs BP Trial: Standard Control: Stroke in the Blood Pressure Trial.36 of 2,363

62 of 2,371

-1.1 points

-1.9 to -0.3

4,734NCT00000620

Action to Control Cardiovascular Risk in Diabetes (ACCORD)

Pregnant Cohort vs Non-pregnant Cohort: Overall Survival39 of 659

570 of 4,073

-8.1 points

-10.0 to -5.8

4,732NCT03673306

Safety of Pregnancy in BRCA Mutated Breast Cancer Patients

Pregnant Cohort vs Non-pregnant Cohort: Breast Cancer-Specific Survival35 of 659

523 of 4,073

-7.5 points

-9.3 to -5.3

4,732NCT03673306

Safety of Pregnancy in BRCA Mutated Breast Cancer Patients

Pregnancy Cohort vs No Pregnancy Cohort: deaths from any cause39 of 659

570 of 4,073

-8.1 points

-10.0 to -5.8

4,732NCT03673306

Safety of Pregnancy in BRCA Mutated Breast Cancer Patients

NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe Acute Gastroenteritis (AGE) Occurring for >7 Days After Dosing Due to GI.1 or GII.4 Norovirus Strains (Excluding Co-infection)1 of 2,355

5 of 2,357

-0.2 points

-0.5 to 0.1

4,712NCT02669121

Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults

NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe AGE Occurring >7 Days After Dosing Due to Any Norovirus Strain (Excluding Co-infection)10 of 2,355

26 of 2,357

-0.7 points

-1.2 to -0.2

4,712NCT02669121

Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults

NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe AGE Occurring >7 Days After Dosing Due to Any Norovirus Strain (Including Co-infection)10 of 2,355

26 of 2,357

-0.7 points

-1.2 to -0.2

4,712NCT02669121

Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults

NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe AGE Occurring >7 Days After Dosing Due to GI.1 or GII.4 Norovirus Strains (Including Co-infection)1 of 2,355

5 of 2,357

-0.2 points

-0.5 to 0.1

4,712NCT02669121

Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults

NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: serious adverse events29 of 2,355

35 of 2,357

-0.3 points

-0.9 to 0.4

4,712NCT02669121

Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults

Early ART vs Deferred ART: AIDs or AIDs Related Death31 of 2,325

83 of 2,359

-2.2 points

-3.1 to -1.3

4,684NCT00867048

Strategic Timing of Antiretroviral Treatment

Early ART vs Deferred ART: Composite Endpoint of AIDS, Serious Non-AIDS Diagnoses, and All-cause Mortality133 of 2,325

215 of 2,359

-3.4 points

-4.9 to -1.9

4,684NCT00867048

Strategic Timing of Antiretroviral Treatment

Early ART vs Deferred ART: Death, All-cause Mortality66 of 2,325

85 of 2,359

-0.8 points

-1.8 to 0.3

4,684NCT00867048

Strategic Timing of Antiretroviral Treatment

Early ART vs Deferred ART: deaths from any cause66 of 2,325

85 of 2,359

-0.8 points

-1.8 to 0.3

4,684NCT00867048

Strategic Timing of Antiretroviral Treatment

Early ART vs Deferred ART: Specific Non-AIDS Diagnoses107 of 2,325

137 of 2,359

-1.2 points

-2.5 to 0.1

4,684NCT00867048

Strategic Timing of Antiretroviral Treatment

Early ART vs Deferred ART: serious adverse events428 of 2,325

500 of 2,359

-2.8 points

-5.1 to -0.5

4,684NCT00867048

Strategic Timing of Antiretroviral Treatment

AZD7442 vs Placebo: The Incidence of Participants Who Have a Post-treatment Response (Negative at Baseline to Positive at Any Time Post-baseline) for SARS-CoV-2 Nucleocapsid Antibodies.198 of 3,121

139 of 1,563

-2.5 points

-4.3 to -1.0

4,684NCT04625725

Phase III Double-blind, Placebo-controlled Study of AZD7442 for Pre-exposure Prophylaxis of COVID-19 in Adult.

Request

GET /api/comparisons/v1

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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Code

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curl "https://conductscience.org/api/comparisons/v1?page=95"

Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=95

{
  "data": {
    "total": 85013,
    "results": [
      {
        "id": "NCT02499679-f8678195",
        "title": "MACE Events Within 90 Days Subject Whose FFRCT Was >0.80 vs MACE Events Within 90 Days. Patients With at Least One FFRCT Value ≤ 0.80: Percentage of Major Adverse Coronary Events (MACE) at 90 Days",
        "summary": "0 of 1592 against 19 of 3145; risk difference -0.6 points, 95% interval -0.9 to -0.3; NCT02499679, Assessing Diagnostic Value of Non-invasive FFRCT in Coronary Care",
        "record": "/library/comparisons/NCT02499679-f8678195",
        "nct_id": "NCT02499679",
        "kind": "outcome",
        "participants": 4737,
        "risk_difference": {
          "value": -0.006041335453100159,
          "lower": -0.009416812924593985,
          "upper": -0.002800273844722289
        },
        "group_1": "0 of 1,592",
        "group_2": "19 of 3,145",
        "difference": "-0.6 points",
        "interval": "-0.9 to -0.3",
        "trial_title": "Assessing Diagnostic Value of Non-invasive FFRCT in Coronary Care"
      },
      {
        "id": "NCT03036124-deaths",
        "title": "Dapa 10mg vs Placebo: deaths from any cause",
        "summary": "286 of 2368 against 333 of 2368; risk difference -2.0 points, 95% interval -3.9 to -0.1; NCT03036124, Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure",
        "record": "/library/comparisons/NCT03036124-deaths",
        "nct_id": "NCT03036124",
        "kind": "deaths",
        "participants": 4736,
        "risk_difference": {
          "value": -0.01984797297297297,
          "lower": -0.03906568896172795,
          "upper": -0.000639261112046513
        },
        "group_1": "286 of 2,368",
        "group_2": "333 of 2,368",
        "difference": "-2.0 points",
        "interval": "-3.9 to -0.1",
        "trial_title": "Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure"
      }
    ],
    "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=96",
  "request_id": "YRhv6HrmTKXlkiZa"
}

Ask about these results. The first 10 go in the prompt.

About this data
Holds
85,013 comparisons
From ClinicalTrials.gov. Counted 10 Nov 2026.
Release
23 Mar 2026
trial-comparisons-2026-03-23-0.1.0
Checked
20 of 20 review comparisons traced to ClinicalTrials.gov, and all 510,078 numbers calculated again apart from the builder agree
Access
Open
No account. 60 calls a minute from one address.

Sources 2

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