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85,013 comparisons from ClinicalTrials.gov.

85,013 comparisons

Most participants first33,758 with no events in either group come last3,301 to 3,320 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
Motavizumab vs Placebo: Number of Participants With RSV Outpatient Medically Attended Lower Respiratory Illness (MA LRI)41 of 1,417

71 of 710

-7.1 points

-9.6 to -4.9

2,127NCT00121108

MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States

Motavizumab vs Placebo: Number of Participants With Medically Attended-Otitis Media (MA-OM) Events532 of 1,417

275 of 710

-1.2 points

-5.6 to 3.2

2,127NCT00121108

MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States

Motavizumab vs Placebo: Number of Participants With Respiratory Syncytial Virus (RSV) Hospitalization21 of 1,417

80 of 710

-9.8 points

-12.4 to -7.5

2,127NCT00121108

MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States

NOMAC-E2 vs DRSP-EE: serious adverse events38 of 1,591

13 of 535

-0.0 points

-1.8 to 1.3

2,126NCT00511199

Efficacy and Safety of the Combined Oral Contraceptive (COC) NOMAC-E2 Compared to a COC Containing DRSP/EE (292001)(COMPLETED)(P05724)

MOTAVIZUMAB vs PLACEBO: deaths from any cause8 of 1,414

5 of 708

-0.1 points

-1.1 to 0.5

2,122NCT00121108

MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States

MOTAVIZUMAB vs PLACEBO: serious adverse events212 of 1,414

148 of 708

-5.9 points

-9.5 to -2.5

2,122NCT00121108

MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States

Old Lina vs New Lina: Frequency of Patients With Adjudication of Cardiac and Cerebrovascular Events82 of 1,532

37 of 589

-0.9 points

-3.4 to 1.2

2,121NCT00736099

Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM

Old Lina vs New Lina: Frequency of Patients With Investigator-defined Hypoglycaemic Adverse Events209 of 1,532

86 of 589

-1.0 points

-4.4 to 2.2

2,121NCT00736099

Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM

Old Lina vs New Lina: serious adverse events158 of 1,532

52 of 589

1.5 points

-1.5 to 4.1

2,121NCT00736099

Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM

MRSA Decolonization vs Education Arm: Rehospitalization Due to MRSA Infection57 of 1,058

83 of 1,063

-2.4 points

-4.6 to -0.3

2,121NCT01209234

Project CLEAR - Changing Lives by Eradicating Antibiotic Resistance

Nirsevimab vs No Intervention: Number of Participants With Hospitalization for All-Cause Lower Respiratory Tract Infection From Days 366 to 731 Post-dosing/Randomization (for United Kingdom Reconsented Participants)18 of 1,096

10 of 1,025

0.7 points

-0.3 to 1.7

2,121NCT05437510

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

VF Induction vs No- VF Induction: Sudden Cardiac Death at Follow up or Resusciation After Ineffective Documented Appropriate ICD Shocks at Follow up10 of 836

12 of 1,284

0.3 points

-0.6 to 1.3

2,120NCT00661037

SAFEty of Two Strategies of ICD Management at Implantation

VF Induction vs no VF Induction: Severe Intra-operative Complications8 of 836

4 of 1,284

0.6 points

-0.0 to 1.6

2,120NCT00661037

SAFEty of Two Strategies of ICD Management at Implantation

VF Induction vs no VF Induction: deaths from any cause108 of 836

188 of 1,284

-1.7 points

-4.7 to 1.3

2,120NCT00661037

SAFEty of Two Strategies of ICD Management at Implantation

VF Induction vs no VF Induction: Number of Participants With Severe Intra-operative Complications at ICD Implant and/or Events at Follow up18 of 836

16 of 1,284

0.9 points

-0.2 to 2.2

2,120NCT00661037

SAFEty of Two Strategies of ICD Management at Implantation

VF Induction vs no VF Induction: serious adverse events209 of 836

177 of 1,284

11.2 points

7.8 to 14.7

2,120NCT00661037

SAFEty of Two Strategies of ICD Management at Implantation

DVS SR 100 mg vs Placebo: Number of Participants With Hepatic Events2 of 1,066

2 of 1,052

-0.0 points

-0.5 to 0.5

2,118NCT00683800

Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women

DVS SR 100 mg vs Placebo: Number of Participants With Adjudicated Cerebrovascular Events - Probable TIA1 of 1,066

0 of 1,052

0.1 points

-0.3 to 0.5

2,118NCT00683800

Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women

DVS SR 100 mg vs Placebo: Number of Participants With Ischemic Heart Disease4 of 1,066

2 of 1,052

0.2 points

-0.4 to 0.8

2,118NCT00683800

Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women

DVS SR 100 mg vs Placebo: serious adverse events43 of 1,066

36 of 1,052

0.6 points

-1.0 to 2.3

2,118NCT00683800

Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women

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.

No key needed

Code

Show the call in
curl "https://conductscience.org/api/comparisons/v1?page=166"

Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=166

{
  "data": {
    "total": 85013,
    "results": [
      {
        "id": "NCT00121108-1a43adaf",
        "title": "Motavizumab vs Placebo: Number of Participants With RSV Outpatient Medically Attended Lower Respiratory Illness (MA LRI)",
        "summary": "41 of 1417 against 71 of 710; risk difference -7.1 points, 95% interval -9.6 to -4.9; NCT00121108, MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States",
        "record": "/library/comparisons/NCT00121108-1a43adaf",
        "nct_id": "NCT00121108",
        "kind": "outcome",
        "participants": 2127,
        "risk_difference": {
          "value": -0.07106563161609034,
          "lower": -0.0964735215881775,
          "upper": -0.04870402940926678
        },
        "group_1": "41 of 1,417",
        "group_2": "71 of 710",
        "difference": "-7.1 points",
        "interval": "-9.6 to -4.9",
        "trial_title": "MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States"
      },
      {
        "id": "NCT00121108-76411a78",
        "title": "Motavizumab vs Placebo: Number of Participants With Medically Attended-Otitis Media (MA-OM) Events",
        "summary": "532 of 1417 against 275 of 710; risk difference -1.2 points, 95% interval -5.6 to 3.2; NCT00121108, MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States",
        "record": "/library/comparisons/NCT00121108-76411a78",
        "nct_id": "NCT00121108",
        "kind": "outcome",
        "participants": 2127,
        "risk_difference": {
          "value": -0.011882870973192683,
          "lower": -0.05590941448863594,
          "upper": 0.03154028816849494
        },
        "group_1": "532 of 1,417",
        "group_2": "275 of 710",
        "difference": "-1.2 points",
        "interval": "-5.6 to 3.2",
        "trial_title": "MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States"
      }
    ],
    "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=167",
  "request_id": "WxOlqYCCTRZ8c74j"
}

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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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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