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85,013 comparisons from ClinicalTrials.gov.
Most participants first33,758 with no events in either group come last3,761 to 3,780 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| GSK1437173A Group vs Placebo Group: Number of Subjects With Any Relapse | 239 of 922 253 of 924 | -1.5 points -5.5 to 2.6 | 1,846 | NCT01610414 Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A |
| GSK1437173A Group vs Placebo Group: deaths from any cause | 118 of 922 124 of 924 | -0.6 points -3.7 to 2.5 | 1,846 | NCT01610414 Study to Evaluate Efficacy, Safety, and Immunogenicity of GlaxoSmithKline (GSK) Biologicals' Herpes Zoster Vaccine GSK1437173A |
| GSK1437173A Group vs Placebo Group: serious adverse events | 329 of 922 310 of 924 | 2.1 points -2.2 to 6.5 | 1,846 | NCT01610414 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 events | 3 of 1,230 0 of 613 | 0.2 points -0.4 to 0.7 | 1,843 | NCT00514709 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 events | 194 of 922 221 of 919 | -3.0 points -6.8 to 0.8 | 1,841 | NCT01064401 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 events | 0 of 774 1 of 1,067 | -0.1 points -0.5 to 0.4 | 1,841 | NCT01108796 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 cause | 45 of 926 55 of 912 | -1.2 points -3.3 to 0.9 | 1,838 | NCT01966471 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 events | 216 of 926 195 of 912 | 1.9 points -1.9 to 5.7 | 1,838 | NCT01966471 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 | 1,836 | NCT02032823 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 | 1,836 | NCT02032823 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 | 1,836 | NCT02032823 Olaparib as Adjuvant Treatment in Patients With Germline BRCA Mutated High Risk HER2 Negative Primary Breast Cancer |
| Olaparib vs Placebo: deaths from any cause | 107 of 921 143 of 915 | -4.0 points -7.2 to -0.9 | 1,836 | NCT02032823 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 | 1,835 | NCT04152161 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 Vaccination | 185 of 918 117 of 917 | 7.4 points 4.0 to 10.8 | 1,835 | NCT04152161 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 cause | 0 of 918 1 of 917 | -0.1 points -0.6 to 0.3 | 1,835 | NCT04152161 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 events | 3 of 918 3 of 917 | -0.0 points -0.7 to 0.7 | 1,835 | NCT04152161 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 cause | 122 of 916 121 of 917 | 0.1 points -3.0 to 3.2 | 1,833 | NCT03068455 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 events | 374 of 916 242 of 917 | 14.4 points 10.1 to 18.7 | 1,833 | NCT03068455 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 Injection | 251 of 919 557 of 910 | -33.9 points -38.1 to -29.5 | 1,829 | NCT06060457 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 Block | 7 of 1,324 14 of 497 | -2.3 points -4.2 to -1.0 | 1,821 | NCT00653133 Multicenter Continuous Peripheral Nerve Block Surveillance Study |
Code
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": {
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"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.
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.
NCBI Gene
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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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