Genes
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 last3,161 to 3,180 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Arm I:Sentinel Node Resection+Conventional Axillary Dissection vs Arm II: Sentinel Node Resection Followed by Node Examination: Morbidity - Number of Participants With Residual Arm Volume Difference | 314 of 1,136 192 of 1,151 | 11.0 points 7.6 to 14.3 | 2,287 | NCT00003830 Surgery to Remove Sentinel Lymph Nodes With or Without Removing Lymph Nodes in the Armpit in Treating Women With Breast Cancer |
| Boostrix Group vs Adacel Group: Number of Subjects With Serious Adverse Events (SAEs). | 9 of 1,522 2 of 762 | 0.3 points -0.4 to 0.9 | 2,284 | NCT00346073 Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years |
| Boostrix Group vs Adacel Group: Number of Subjects With Any Unsolicited Adverse Events (AEs) | 271 of 1,522 169 of 762 | -4.4 points -8.0 to -0.9 | 2,284 | NCT00346073 Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years |
| Boostrix Group vs Adacel Group: deaths from any cause | 1 of 1,522 1 of 762 | -0.1 points -0.7 to 0.3 | 2,284 | NCT00346073 Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years |
| Boostrix Group vs Adacel Group: serious adverse events | 21 of 1,522 13 of 762 | -0.3 points -1.6 to 0.7 | 2,284 | NCT00346073 Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years |
| Enrolled Set vs Follow-Up Set: deaths from any cause | 32 of 1,415 30 of 861 | -1.2 points -2.8 to 0.2 | 2,276 | NCT02807857 A Prospective Evaluation of Natriuretic Peptide Based Referral of CHF Patients in Primary Care |
| Enrolled Set vs Follow-Up Set: serious adverse events | 117 of 1,415 114 of 861 | -5.0 points -7.7 to -2.4 | 2,276 | NCT02807857 A Prospective Evaluation of Natriuretic Peptide Based Referral of CHF Patients in Primary Care |
| Darbepoetin Alfa vs Placebo: serious adverse events | 781 of 1,133 741 of 1,140 | 3.9 points 0.1 to 7.8 | 2,273 | NCT00358215 RED-HF™ Trial - Reduction of Events With Darbepoetin Alfa in Heart Failure Trial |
| GSK1572932 Group vs Placebo Group: Number of Patients With Serious Adverse Events (SAEs) - Up to Data Lock Point (DLP) | 330 of 1,515 164 of 757 | 0.1 points -3.6 to 3.6 | 2,272 | NCT00480025 GSK1572932A Antigen-Specific Cancer Immunotherapeutic as Adjuvant Therapy in Patients With Non-Small Cell Lung Cancer |
| GSK1572932 Group vs Placebo Group: deaths from any cause | 30 of 1,515 17 of 757 | -0.3 points -1.7 to 0.9 | 2,272 | NCT00480025 GSK1572932A Antigen-Specific Cancer Immunotherapeutic as Adjuvant Therapy in Patients With Non-Small Cell Lung Cancer |
| GSK1572932 Group vs Placebo Group: serious adverse events | 330 of 1,515 164 of 757 | 0.1 points -3.6 to 3.6 | 2,272 | NCT00480025 GSK1572932A Antigen-Specific Cancer Immunotherapeutic as Adjuvant Therapy in Patients With Non-Small Cell Lung Cancer |
| Anti-hypertensive Therapy to Goal <140/90 mmHg vs No Anti-hypertensive Unless BP is Severe (≥160/105 mmHg: Small for Gestational Age (Safety) | 128 of 1,146 117 of 1,124 | 0.8 points -1.8 to 3.3 | 2,270 | NCT02299414 Chronic Hypertension and Pregnancy (CHAP) Project |
| Absorb BVS vs XIENCE: Number of Participants With Repeat Coronary Arteriography | 225 of 1,125 237 of 1,144 | -0.7 points -4.0 to 2.6 | 2,269 | NCT02173379 Absorb IV Randomized Controlled Trial |
| Whole Breast Irradiation + Sequential Boost vs Hypofractionated Whole Breast Irradiation + Concurrent Boost: deaths from any cause | 87 of 1,124 86 of 1,138 | 0.2 points -2.0 to 2.4 | 2,262 | NCT01349322 Higher Per Daily Treatment-Dose Radiation Therapy or Standard Per Daily Treatment Radiation Therapy in Treating Patients With Early-Stage Breast Cancer That Was Removed by Surgery |
| COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based All-cause Hospital Readmissions | 210 of 1,069 222 of 1,193 | 1.0 points -2.2 to 4.3 | 2,262 | NCT02588664 Comprehensive Post-Acute Stroke Services |
| COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based All-cause Hospital Readmissions | 485 of 1,069 516 of 1,193 | 2.1 points -2.0 to 6.2 | 2,262 | NCT02588664 Comprehensive Post-Acute Stroke Services |
| COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based Admissions to Skilled Nursing Facilities (SNF) and Inpatient Rehabilitation Facilities (IRF) | 150 of 1,069 142 of 1,193 | 2.1 points -0.6 to 4.9 | 2,262 | NCT02588664 Comprehensive Post-Acute Stroke Services |
| COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based Emergency Department Visits | 626 of 1,069 691 of 1,193 | 0.6 points -3.4 to 4.7 | 2,262 | NCT02588664 Comprehensive Post-Acute Stroke Services |
| COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based Use of Transitional Care Management Billing Codes | 345 of 1,069 239 of 1,193 | 12.2 points 8.6 to 15.8 | 2,262 | NCT02588664 Comprehensive Post-Acute Stroke Services |
| COMPASS Intervention vs Usual Care: Number of Subjects With Claims-based All-cause Hospital Readmissions | 105 of 1,069 103 of 1,193 | 1.2 points -1.2 to 3.6 | 2,262 | NCT02588664 Comprehensive Post-Acute Stroke Services |
Code
curl "https://conductscience.org/api/comparisons/v1?page=159"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=159
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00003830-305607ae",
"title": "Arm I:Sentinel Node Resection+Conventional Axillary Dissection vs Arm II: Sentinel Node Resection Followed by Node Examination: Morbidity - Number of Participants With Residual Arm Volume Difference",
"summary": "314 of 1136 against 192 of 1151; risk difference 11.0 points, 95% interval 7.6 to 14.3; NCT00003830, Surgery to Remove Sentinel Lymph Nodes With or Without Removing Lymph Nodes in the Armpit in Treating Women With Breast Cancer",
"record": "/library/comparisons/NCT00003830-305607ae",
"nct_id": "NCT00003830",
"kind": "outcome",
"participants": 2287,
"risk_difference": {
"value": 0.10959698241578053,
"lower": 0.07570672079313154,
"upper": 0.1432331139406867
},
"group_1": "314 of 1,136",
"group_2": "192 of 1,151",
"difference": "11.0 points",
"interval": "7.6 to 14.3",
"trial_title": "Surgery to Remove Sentinel Lymph Nodes With or Without Removing Lymph Nodes in the Armpit in Treating Women With Breast Cancer"
},
{
"id": "NCT00346073-02f59107",
"title": "Boostrix Group vs Adacel Group: Number of Subjects With Serious Adverse Events (SAEs).",
"summary": "9 of 1522 against 2 of 762; risk difference 0.3 points, 95% interval -0.4 to 0.9; NCT00346073, Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years",
"record": "/library/comparisons/NCT00346073-02f59107",
"nct_id": "NCT00346073",
"kind": "outcome",
"participants": 2284,
"risk_difference": {
"value": 0.0032886000945019853,
"lower": -0.004152249300190166,
"upper": 0.008908194643430064
},
"group_1": "9 of 1,522",
"group_2": "2 of 762",
"difference": "0.3 points",
"interval": "-0.4 to 0.9",
"trial_title": "Safety and Immunogenicity of GSK's Tdap Vaccine (Boostrix) in Adults Aged 19 to 64 Years"
}
],
"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=160",
"request_id": "lR290NZK4Pt7KGoV"
}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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Opens sequences.conductscience.org
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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