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85,013 comparisons from ClinicalTrials.gov.

85,013 comparisons

Most participants first33,758 with no events in either group come last3,761 to 3,780 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
GSK1437173A Group vs Placebo Group: Number of Subjects With Any Relapse239 of 922

253 of 924

-1.5 points

-5.5 to 2.6

1,846NCT01610414

Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A

GSK1437173A Group vs Placebo Group: deaths from any cause118 of 922

124 of 924

-0.6 points

-3.7 to 2.5

1,846NCT01610414

Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A

GSK1437173A Group vs Placebo Group: serious adverse events329 of 922

310 of 924

2.1 points

-2.2 to 6.5

1,846NCT01610414

Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A

Group 1: DTaP-Hep B-PRP~T + OPV vs Group 2: Tritanrix-Hep B/ Hib™ + OPV: serious adverse events3 of 1,230

0 of 613

0.2 points

-0.4 to 0.7

1,843NCT00514709

Immunogenicity Study of Antibody Persistence and Booster Effect of DTaP-HB PRP~T Combined Vaccine in Filipino Infants

IFN Beta-1a 30 mcg vs DAC HYP 150 mg: serious adverse events194 of 922

221 of 919

-3.0 points

-6.8 to 0.8

1,841NCT01064401

Efficacy and Safety of BIIB019 (Daclizumab High Yield Process) Versus Interferon β 1a in Participants With Relapsing-Remitting Multiple Sclerosis

Micardis® (Telmisartan) vs MicardisPlus® (Telmisartan Hydrochlorothiazide): serious adverse events0 of 774

1 of 1,067

-0.1 points

-0.5 to 0.4

1,841NCT01108796

Additional Effect of A Life Style Program on Antihypertensive Treatment With Telmisartan

Anthracycline Followed by Trastuzumab, Pertuzumab, and Taxane vs Anthracycline Followed by Trastuzumab Emtansine and Pertuzumab: deaths from any cause45 of 926

55 of 912

-1.2 points

-3.3 to 0.9

1,838NCT01966471

A Study of Trastuzumab Emtansine (Kadcyla) Plus Pertuzumab (Perjeta) Following Anthracyclines in Comparison With Trastuzumab (Herceptin) Plus Pertuzumab and a Taxane Following Anthracyclines as Adjuvant Therapy in Participants With Operable HER2-Positive Primary Breast Cancer

Anthracycline Followed by Trastuzumab, Pertuzumab, and Taxane vs Anthracycline Followed by Trastuzumab Emtansine and Pertuzumab: serious adverse events216 of 926

195 of 912

1.9 points

-1.9 to 5.7

1,838NCT01966471

A Study of Trastuzumab Emtansine (Kadcyla) Plus Pertuzumab (Perjeta) Following Anthracyclines in Comparison With Trastuzumab (Herceptin) Plus Pertuzumab and a Taxane Following Anthracyclines as Adjuvant Therapy in Participants With Operable HER2-Positive Primary Breast Cancer

Olaparib vs Placebo: Distant Disease Free Survival (DDFS)89 of 921

152 of 915

-6.9 points

-10.0 to -3.9

1,836NCT02032823

Olaparib as Adjuvant Treatment in Patients With Germline BRCA Mutated High Risk HER2 Negative Primary Breast Cancer

Olaparib vs Placebo: Invasive Disease Free Survival (IDFS)106 of 921

178 of 915

-7.9 points

-11.2 to -4.6

1,836NCT02032823

Olaparib as Adjuvant Treatment in Patients With Germline BRCA Mutated High Risk HER2 Negative Primary Breast Cancer

Olaparib vs Placebo: Overall Survival (OS)75 of 921

109 of 915

-3.8 points

-6.5 to -1.0

1,836NCT02032823

Olaparib as Adjuvant Treatment in Patients With Germline BRCA Mutated High Risk HER2 Negative Primary Breast Cancer

Olaparib vs Placebo: deaths from any cause107 of 921

143 of 915

-4.0 points

-7.2 to -0.9

1,836NCT02032823

Olaparib as Adjuvant Treatment in Patients With Germline BRCA Mutated High Risk HER2 Negative Primary Breast Cancer

Bacille Calmette Guerin (BCG) Group vs Placebo Group: Number of Participants With Serious Adverse Events (SAEs)3 of 918

3 of 917

-0.0 points

-0.7 to 0.7

1,835NCT04152161

Bacille Calmette Guerin (BCG) Revaccination of Healthy Adolescents for the Prevention of Mycobacterium Tuberculosis Sustained Infection

Bacille Calmette Guerin (BCG) Group vs Placebo Group: Number of Participants With Unsolicited AEs Through Day 28, as Well as Solicited AEs That Were Ongoing at Day 7 After Vaccination185 of 918

117 of 917

7.4 points

4.0 to 10.8

1,835NCT04152161

Bacille Calmette Guerin (BCG) Revaccination of Healthy Adolescents for the Prevention of Mycobacterium Tuberculosis Sustained Infection

Bacille Calmette Guerin (BCG) Group vs Placebo Group: deaths from any cause0 of 918

1 of 917

-0.1 points

-0.6 to 0.3

1,835NCT04152161

Bacille Calmette Guerin (BCG) Revaccination of Healthy Adolescents for the Prevention of Mycobacterium Tuberculosis Sustained Infection

Bacille Calmette Guerin (BCG) Group vs Placebo Group: serious adverse events3 of 918

3 of 917

-0.0 points

-0.7 to 0.7

1,835NCT04152161

Bacille Calmette Guerin (BCG) Revaccination of Healthy Adolescents for the Prevention of Mycobacterium Tuberculosis Sustained Infection

Arm A: Nivo + Ipi vs Arm B: Nivo: deaths from any cause122 of 916

121 of 917

0.1 points

-3.0 to 3.2

1,833NCT03068455

An Investigational Immuno-therapy Study of Nivolumab Combined With Ipilimumab Compared to Nivolumab by Itself After Complete Surgical Removal of Stage IIIb/c/d or Stage IV Melanoma

Arm A: Nivo + Ipi vs Arm B: Nivo: serious adverse events374 of 916

242 of 917

14.4 points

10.1 to 18.7

1,833NCT03068455

An Investigational Immuno-therapy Study of Nivolumab Combined With Ipilimumab Compared to Nivolumab by Itself After Complete Surgical Removal of Stage IIIb/c/d or Stage IV Melanoma

Fluzone HD + mRNA-1345 Followed by Placebo vs Fluzone HD + Placebo Followed by mRNA-1345: Number of Participants With Solicited Local and Systemic ARs Within 7 Days After Day 22 Injection251 of 919

557 of 910

-33.9 points

-38.1 to -29.5

1,829NCT06060457

A Study to Evaluate the Safety and Immune Response of mRNA-1345, a Vaccine Targeting Respiratory Syncytial Virus (RSV), When Co-administered With a Fluzone HD, in Adults ≥65 Years of Age

USPNB vs NSPNB: Complications of Peripheral Nerve Block7 of 1,324

14 of 497

-2.3 points

-4.2 to -1.0

1,821NCT00653133

Multicenter Continuous Peripheral Nerve Block Surveillance Study

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=189"

Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=189

{
  "data": {
    "total": 85013,
    "results": [
      {
        "id": "NCT01610414-137b3fed",
        "title": "GSK1437173A Group vs Placebo Group: Number of Subjects With Any Relapse",
        "summary": "239 of 922 against 253 of 924; risk difference -1.5 points, 95% interval -5.5 to 2.6; NCT01610414, Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A",
        "record": "/library/comparisons/NCT01610414-137b3fed",
        "nct_id": "NCT01610414",
        "kind": "outcome",
        "participants": 1846,
        "risk_difference": {
          "value": -0.014590434872430558,
          "lower": -0.054852742676134054,
          "upper": 0.0257380528554206
        },
        "group_1": "239 of 922",
        "group_2": "253 of 924",
        "difference": "-1.5 points",
        "interval": "-5.5 to 2.6",
        "trial_title": "Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A"
      },
      {
        "id": "NCT01610414-deaths",
        "title": "GSK1437173A Group vs Placebo Group: deaths from any cause",
        "summary": "118 of 922 against 124 of 924; risk difference -0.6 points, 95% interval -3.7 to 2.5; NCT01610414, Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A",
        "record": "/library/comparisons/NCT01610414-deaths",
        "nct_id": "NCT01610414",
        "kind": "deaths",
        "participants": 1846,
        "risk_difference": {
          "value": -0.006216487778309909,
          "lower": -0.037094499966359454,
          "upper": 0.0246618220861712
        },
        "group_1": "118 of 922",
        "group_2": "124 of 924",
        "difference": "-0.6 points",
        "interval": "-3.7 to 2.5",
        "trial_title": "Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A"
      }
    ],
    "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=190",
  "request_id": "B1KDYZFUpHsj4g43"
}

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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Every answer on this page is also JSON, under /api/comparisons/v1. No key.

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