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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 last201 to 220 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase)575 of 21,898

1,189 of 21,890

-2.8 points

-3.2 to -2.4

43,788NCT04505722

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants

Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Medically-Attended Adverse Events (MAAEs) (Double Blind Phase)1,672 of 21,894

1,885 of 21,882

-1.0 points

-1.5 to -0.5

43,776NCT04505722

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants

Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Adverse Events of Special Interest (AESI) (Double Blind Phase)6 of 21,894

5 of 21,882

0.0 points

-0.0 to 0.0

43,776NCT04505722

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants

Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With MAAEs Leading to Study Discontinuation (Double Blind Phase)1 of 21,894

2 of 21,882

-0.0 points

-0.0 to 0.0

43,776NCT04505722

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants

Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Serious Adverse Events (SAEs) (Double Blind Phase)235 of 21,894

358 of 21,882

-0.6 points

-0.8 to -0.3

43,776NCT04505722

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants

FluNG Group vs Fluarix Group: serious adverse events4,071 of 21,893

4,066 of 21,802

-0.1 points

-0.8 to 0.7

43,695NCT00753272

Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older

FluNG Group vs Fluarix Group: Number of Subjects Reporting Polymerase Chain Reaction (PCR)-Confirmed Influenza A and/or B Infection.274 of 21,573

310 of 21,482

-0.2 points

-0.4 to 0.0

43,055NCT00753272

Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older

Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase)487 of 21,537

1,079 of 21,467

-2.8 points

-3.1 to -2.4

43,004NCT04505722

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants

FluNG Group vs Fluarix Group: Number of Subjects Reporting All-cause Death After the First Dose of Vaccine.63 of 21,394

88 of 21,337

-0.1 points

-0.2 to -0.0

42,731NCT00753272

Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older

FluNG Group vs Fluarix Group: Number of Subjects Reporting Hospitalization Due to Respiratory Diseases After the First Dose of Vaccine84 of 21,394

89 of 21,337

-0.0 points

-0.1 to 0.1

42,731NCT00753272

Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older

FluNG Group vs Fluarix Group: Number of Subjects Reporting Pneumonia or Clinical Influenza After the First Dose of Vaccine.202 of 21,394

225 of 21,337

-0.1 points

-0.3 to 0.1

42,731NCT00753272

Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older

Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase)436 of 21,244

895 of 20,978

-2.2 points

-2.5 to -1.9

42,222NCT04505722

A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants

EHR-facilitated Collaborative Care (Intervention) vs Usual Care (Control): Number of Deceased Participants3,192 of 24,874

2,214 of 16,180

-0.9 points

-1.5 to -0.2

41,054NCT03892967

Enhanced, EHR-facilitated Cancer Symptom Control Pragmatic Clinical Trial

EHR-facilitated Collaborative Care (Intervention) vs Usual Care (Control): deaths from any cause3,192 of 24,874

2,214 of 16,180

-0.9 points

-1.5 to -0.2

41,054NCT03892967

Enhanced, EHR-facilitated Cancer Symptom Control Pragmatic Clinical Trial

FluNG Group vs Fluarix Group: Number of Subjects Reporting Polymerase Chain Reaction (PCR)-Confirmed Influenza A and/or B Infection.262 of 20,579

296 of 20,458

-0.2 points

-0.4 to 0.1

41,037NCT00753272

Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older

FluNG Group vs Fluarix Group: Number of Subjects Reporting Culture-confirmed Influenza A and/or B Infection.144 of 20,579

145 of 20,458

-0.0 points

-0.2 to 0.2

41,037NCT00753272

Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older

Matched Treated: Long-term Disability vs Matched Untreated: Long-term Disability: Number of Participants With Any Long Term Disability (LTD) Claim: Matched Participants50 of 20,318

74 of 20,318

-0.1 points

-0.2 to -0.0

40,636NCT07072793

A US Study to Look at Loss of Work and Healthcare Costs for People Affected With Mild-to-moderate COVID 19 Who Have High Chances of the Disease Becoming Severe

Female Cases vs Female Controls: Number of New Onset Skin Cancers in the Female Sex Subgroup78 of 8,159

429 of 32,121

-0.4 points

-0.6 to -0.1

40,280NCT04969419

Incidence of Melanoma and Non-melanoma Skin Cancer in People With Vitiligo

Matched Treated: Short-term Disability vs Matched Untreated: Short-term Disability: Number of Participants With Any Short Term Disability (STD) Claim: Matched Participants1,343 of 20,065

1,848 of 20,065

-2.5 points

-3.0 to -2.0

40,130NCT07072793

A US Study to Look at Loss of Work and Healthcare Costs for People Affected With Mild-to-moderate COVID 19 Who Have High Chances of the Disease Becoming Severe

eSyM Control Participants (Medical Oncology and Surgery Participants Combined) vs eSyM Intervention Participants (Medical Oncology and Surgery Participants Combined): deaths from any cause4,898 of 21,112

4,161 of 18,830

1.1 points

0.3 to 1.9

39,942NCT03850912

Symptom Management Implementation of Patient Reported Outcomes in Oncology

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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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Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=11

{
  "data": {
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      {
        "id": "NCT04505722-e20eadc8",
        "title": "Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase)",
        "summary": "575 of 21898 against 1189 of 21890; risk difference -2.8 points, 95% interval -3.2 to -2.4; NCT04505722, A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants",
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        },
        "group_1": "575 of 21,898",
        "group_2": "1,189 of 21,890",
        "difference": "-2.8 points",
        "interval": "-3.2 to -2.4",
        "trial_title": "A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants"
      },
      {
        "id": "NCT04505722-89e40f6c",
        "title": "Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Medically-Attended Adverse Events (MAAEs) (Double Blind Phase)",
        "summary": "1672 of 21894 against 1885 of 21882; risk difference -1.0 points, 95% interval -1.5 to -0.5; NCT04505722, A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants",
        "record": "/library/comparisons/NCT04505722-89e40f6c",
        "nct_id": "NCT04505722",
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        "participants": 43776,
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          "lower": -0.014897463089226789,
          "upper": -0.004657710983545815
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        "group_1": "1,672 of 21,894",
        "group_2": "1,885 of 21,882",
        "difference": "-1.0 points",
        "interval": "-1.5 to -0.5",
        "trial_title": "A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants"
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      "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"
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      "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.",
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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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