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85,013 comparisons from ClinicalTrials.gov.

85,013 comparisons

Most participants first33,758 with no events in either group come last4,981 to 5,000 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: deaths from any cause1 of 961

0 of 245

0.1 points

-1.4 to 0.6

1,206NCT00449670

Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults

H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: serious adverse events25 of 961

5 of 245

0.6 points

-2.2 to 2.2

1,206NCT00449670

Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults

Clinically Driven Monitoring (CDM) vs Laboratory Plus Clinical Monitoring (LCM): LCM vs CDM: New Grade 3 or 4 Adverse Event (AE), Not Solely Related to HIV283 of 606

282 of 600

-0.3 points

-5.9 to 5.3

1,206NCT02028676

Efficacy Study of Different Laboratory Management Strategies and Drug Regimens in HIV-infected Children in Africa

Clinically Driven Monitoring (CDM) vs Laboratory Plus Clinical Monitoring (LCM): LCM vs CDM: Disease Progression to a New WHO Stage 4 Event or Death47 of 606

39 of 600

1.3 points

-1.7 to 4.2

1,206NCT02028676

Efficacy Study of Different Laboratory Management Strategies and Drug Regimens in HIV-infected Children in Africa

Clinically Driven Monitoring (CDM) vs Laboratory Plus Clinical Monitoring (LCM): LCM vs CDM, Induction ART: Cessation of First-line Regimen for Clinical/Immunological Failure28 of 606

35 of 600

-1.2 points

-3.8 to 1.3

1,206NCT02028676

Efficacy Study of Different Laboratory Management Strategies and Drug Regimens in HIV-infected Children in Africa

Acoziborole vs Placebo: Occurrence of TEAEs - Headache53 of 906

8 of 300

3.2 points

0.3 to 5.3

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of Serious TEAEs3 of 906

4 of 300

-1.0 points

-3.1 to 0.0

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Gastritis6 of 906

3 of 300

-0.3 points

-2.3 to 0.7

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Fatigue14 of 906

5 of 300

-0.1 points

-2.4 to 1.3

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of Adverse Events (AEs)195 of 906

69 of 300

-1.5 points

-7.2 to 3.7

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of Any Treatment-related TEAEs59 of 906

17 of 300

0.8 points

-2.7 to 3.6

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Acarodermatitis13 of 906

3 of 300

0.4 points

-1.6 to 1.6

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Nausea7 of 906

3 of 300

-0.2 points

-2.2 to 0.8

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Malaria34 of 906

14 of 300

-0.9 points

-4.1 to 1.4

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Abdominal Pain23 of 906

9 of 300

-0.5 points

-3.2 to 1.4

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Blood Potassium Increased8 of 906

6 of 300

-1.1 points

-3.5 to 0.3

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: deaths from any cause0 of 906

1 of 300

-0.3 points

-1.9 to 0.2

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of TEAEs - Enteritis7 of 906

4 of 300

-0.6 points

-2.6 to 0.6

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: Occurrence of Any TEAEs195 of 906

69 of 300

-1.5 points

-7.2 to 3.7

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

Acoziborole vs Placebo: serious adverse events3 of 906

4 of 300

-1.0 points

-3.1 to 0.0

1,206NCT05256017

Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects

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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curl "https://conductscience.org/api/comparisons/v1?page=250"

Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=250

{
  "data": {
    "total": 85013,
    "results": [
      {
        "id": "NCT00449670-deaths",
        "title": "H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: deaths from any cause",
        "summary": "1 of 961 against 0 of 245; risk difference 0.1 points, 95% interval -1.4 to 0.6; NCT00449670, Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults",
        "record": "/library/comparisons/NCT00449670-deaths",
        "nct_id": "NCT00449670",
        "kind": "deaths",
        "participants": 1206,
        "risk_difference": {
          "value": 0.001040582726326743,
          "lower": -0.014420554442176596,
          "upper": 0.005870607850164397
        },
        "group_1": "1 of 961",
        "group_2": "0 of 245",
        "difference": "0.1 points",
        "interval": "-1.4 to 0.6",
        "trial_title": "Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults"
      },
      {
        "id": "NCT00449670-sae",
        "title": "H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: serious adverse events",
        "summary": "25 of 961 against 5 of 245; risk difference 0.6 points, 95% interval -2.2 to 2.2; NCT00449670, Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults",
        "record": "/library/comparisons/NCT00449670-sae",
        "nct_id": "NCT00449670",
        "kind": "serious-adverse-events",
        "participants": 1206,
        "risk_difference": {
          "value": 0.005606404892862453,
          "lower": -0.02214179846030292,
          "upper": 0.02241526310445212
        },
        "group_1": "25 of 961",
        "group_2": "5 of 245",
        "difference": "0.6 points",
        "interval": "-2.2 to 2.2",
        "trial_title": "Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults"
      }
    ],
    "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=251",
  "request_id": "poyHlZTaWi9nthWW"
}

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
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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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