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NCBI Gene
One gene with its proteins, patents, drugs, trials, grants and papers.
85,013 comparisons from ClinicalTrials.gov.
Most participants first33,758 with no events in either group come last3,321 to 3,340 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Flulaval Group vs Fluzone Group: Number of Subjects Reporting Medically Attended Adverse Events (MAEs). | 447 of 1,055 432 of 1,061 | 1.7 points -2.5 to 5.8 | 2,116 | NCT00980005 Study to Assess the Immunogenicity and Safety of an Investigational Influenza Vaccine in Children |
| Flulaval Group vs Fluzone Group: Number of Subjects Reporting Serious Adverse Events (SAEs). | 10 of 1,055 6 of 1,061 | 0.4 points -0.4 to 1.2 | 2,116 | NCT00980005 Study to Assess the Immunogenicity and Safety of an Investigational Influenza Vaccine in Children |
| Flulaval Group vs Fluzone Group: serious adverse events | 10 of 1,055 6 of 1,061 | 0.4 points -0.4 to 1.2 | 2,116 | NCT00980005 Study to Assess the Immunogenicity and Safety of an Investigational Influenza Vaccine in Children |
| On Pump vs Off Pump: Long-term Composite | 78 of 1,050 105 of 1,061 | -2.5 points -4.9 to -0.1 | 2,111 | NCT00032630 Outcomes Following Myocardial Revascularization: On and Off Cardiopulmonary Bypass |
| General Anesthesia and Opioid vs Regional Analgesia and Propofol: Number of Participants Who Had Breast Cancer Recurrence After Breast Cancer Surgery | 111 of 1,065 102 of 1,043 | 0.6 points -1.9 to 3.2 | 2,108 | NCT00418457 Regional Anesthesia and Breast Cancer Recurrence |
| General Anesthesia and Opioid vs Regional Analgesia and Propofol: deaths from any cause | 22 of 1,065 18 of 1,043 | 0.3 points -0.9 to 1.6 | 2,108 | NCT00418457 Regional Anesthesia and Breast Cancer Recurrence |
| Treatment Arm 1: OKZ 64 mg q4w + MTX vs Treatment Arm 2: OKZ 64 mg q2w + MTX: Incidence of Treatment-Emergent AEs Leading to Withdrawal of the Study Treatment | 87 of 1,043 90 of 1,061 | -0.1 points -2.5 to 2.2 | 2,104 | NCT03120949 Efficacy and Safety of Olokizumab in Subjects With Moderately to Severely Active Rheumatoid Arthritis |
| Treatment Arm 1: OKZ 64 mg q4w + MTX vs Treatment Arm 2: OKZ 64 mg q2w + MTX: deaths from any cause | 13 of 1,043 13 of 1,061 | 0.0 points -1.0 to 1.0 | 2,104 | NCT03120949 Efficacy and Safety of Olokizumab in Subjects With Moderately to Severely Active Rheumatoid Arthritis |
| Treatment Arm 1: OKZ 64 mg q4w + MTX vs Treatment Arm 2: OKZ 64 mg q2w + MTX: serious adverse events | 129 of 1,043 120 of 1,061 | 1.1 points -1.7 to 3.8 | 2,104 | NCT03120949 Efficacy and Safety of Olokizumab in Subjects With Moderately to Severely Active Rheumatoid Arthritis |
| Precision Strategy (PS) vs Usual Testing (UT): deaths from any cause | 5 of 1,057 7 of 1,046 | -0.2 points -1.0 to 0.5 | 2,103 | NCT03702244 The PRECISE Protocol: Prospective Randomized Trial of the Optimal Evaluation of Cardiac Symptoms and Revascularization |
| Precision Strategy (PS) vs Usual Testing (UT): serious adverse events | 40 of 1,057 30 of 1,046 | 0.9 points -0.6 to 2.5 | 2,103 | NCT03702244 The PRECISE Protocol: Prospective Randomized Trial of the Optimal Evaluation of Cardiac Symptoms and Revascularization |
| Adherence Intervention vs Usual Care: Statin Medication Adherence | 586 of 1,063 529 of 1,039 | 4.2 points -0.1 to 8.5 | 2,102 | NCT03748420 Medication Adherence Clinical Decision Support |
| Dapsone Gel vs Dapsone Gel Vehicle: serious adverse events | 3 of 1,044 5 of 1,057 | -0.2 points -0.8 to 0.4 | 2,101 | NCT01974141 A Safety and Efficacy Study of Dapsone Gel in Patients With Acne Vulgaris |
| Roxadustat vs Epoetin Alfa: deaths from any cause | 247 of 1,048 231 of 1,053 | 1.6 points -2.0 to 5.2 | 2,101 | NCT02174731 Safety and Efficacy Study of Roxadustat to Treat Anemia in Patients With Chronic Kidney Disease, on Dialysis. |
| Roxadustat vs Epoetin Alfa: serious adverse events | 604 of 1,048 606 of 1,053 | 0.1 points -4.1 to 4.3 | 2,101 | NCT02174731 Safety and Efficacy Study of Roxadustat to Treat Anemia in Patients With Chronic Kidney Disease, on Dialysis. |
| Intervention vs Control: deaths from any cause | 119 of 1,051 134 of 1,049 | -1.5 points -4.2 to 1.3 | 2,100 | NCT02811432 Kangaroo Mother Care Before Stabilisation Amongst Low Birth Weight Neonates in Africa |
| Intervention vs Control: Mortality Within 28 Days | 119 of 1,051 134 of 1,049 | -1.5 points -4.2 to 1.3 | 2,100 | NCT02811432 Kangaroo Mother Care Before Stabilisation Amongst Low Birth Weight Neonates in Africa |
| Intervention vs Control: serious adverse events | 124 of 1,051 125 of 1,049 | -0.1 points -2.9 to 2.7 | 2,100 | NCT02811432 Kangaroo Mother Care Before Stabilisation Amongst Low Birth Weight Neonates in Africa |
| QIV-HD vs QIV-SD: Number of Participants Reporting Unsolicited Adverse Events (AEs) | 71 of 1,049 85 of 1,051 | -1.3 points -3.6 to 0.9 | 2,100 | NCT04498832 Study to Assess the Immune Response and the Safety Profile of a High-Dose Quadrivalent Influenza Vaccine (QIV-HD) Compared to a Standard-Dose Quadrivalent Influenza Vaccine (QIV-SD) in Japanese Adults 60 Years of Age and Older |
| QIV-HD vs QIV-SD: Number of Participants Reporting Immediate Unsolicited Adverse Events (AEs) | 0 of 1,049 1 of 1,051 | -0.1 points -0.5 to 0.3 | 2,100 | NCT04498832 Study to Assess the Immune Response and the Safety Profile of a High-Dose Quadrivalent Influenza Vaccine (QIV-HD) Compared to a Standard-Dose Quadrivalent Influenza Vaccine (QIV-SD) in Japanese Adults 60 Years of Age and Older |
Code
curl "https://conductscience.org/api/comparisons/v1?page=167"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=167
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00980005-48fe9545",
"title": "Flulaval Group vs Fluzone Group: Number of Subjects Reporting Medically Attended Adverse Events (MAEs).",
"summary": "447 of 1055 against 432 of 1061; risk difference 1.7 points, 95% interval -2.5 to 5.8; NCT00980005, Study to Assess the Immunogenicity and Safety of an Investigational Influenza Vaccine in Children",
"record": "/library/comparisons/NCT00980005-48fe9545",
"nct_id": "NCT00980005",
"kind": "outcome",
"participants": 2116,
"risk_difference": {
"value": 0.016533628741552064,
"lower": -0.02542267247686221,
"upper": 0.058411493242981095
},
"group_1": "447 of 1,055",
"group_2": "432 of 1,061",
"difference": "1.7 points",
"interval": "-2.5 to 5.8",
"trial_title": "Study to Assess the Immunogenicity and Safety of an Investigational Influenza Vaccine in Children"
},
{
"id": "NCT00980005-d66edafc",
"title": "Flulaval Group vs Fluzone Group: Number of Subjects Reporting Serious Adverse Events (SAEs).",
"summary": "10 of 1055 against 6 of 1061; risk difference 0.4 points, 95% interval -0.4 to 1.2; NCT00980005, Study to Assess the Immunogenicity and Safety of an Investigational Influenza Vaccine in Children",
"record": "/library/comparisons/NCT00980005-d66edafc",
"nct_id": "NCT00980005",
"kind": "outcome",
"participants": 2116,
"risk_difference": {
"value": 0.003823630572963895,
"lower": -0.004088620372311018,
"upper": 0.012278317498428469
},
"group_1": "10 of 1,055",
"group_2": "6 of 1,061",
"difference": "0.4 points",
"interval": "-0.4 to 1.2",
"trial_title": "Study to Assess the Immunogenicity and Safety of an Investigational Influenza Vaccine in Children"
}
],
"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"
},
{
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},
{
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],
"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=168",
"request_id": "d7QGC8ss0iiEvrXx"
}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
One gene with its proteins, patents, drugs, trials, grants and papers.
ClinicalTrials.gov
Search clinical trials by condition, drug, outcome or NCT number, with the results each one posted.
Patent publications
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For software
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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