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 last1,881 to 1,900 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| MACE Events Within 90 Days Subject Whose FFRCT Was >0.80 vs MACE Events Within 90 Days. Patients With at Least One FFRCT Value ≤ 0.80: Percentage of Major Adverse Coronary Events (MACE) at 90 Days | 0 of 1,592 19 of 3,145 | -0.6 points -0.9 to -0.3 | 4,737 | NCT02499679 Assessing Diagnostic Value of Non-invasive FFRCT in Coronary Care |
| Dapa 10mg vs Placebo: deaths from any cause | 286 of 2,368 333 of 2,368 | -2.0 points -3.9 to -0.1 | 4,736 | NCT03036124 Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure |
| Dapa 10mg vs Placebo: serious adverse events | 895 of 2,368 994 of 2,368 | -4.2 points -7.0 to -1.4 | 4,736 | NCT03036124 Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure |
| BP Trial: Intensive Control vs BP Trial: Standard Control: First Occurrence of Major Cardiovascular Event (MCE) in the Blood Pressure Trial. | 208 of 2,363 237 of 2,371 | -1.2 points -2.9 to 0.5 | 4,734 | NCT00000620 Action to Control Cardiovascular Risk in Diabetes (ACCORD) |
| BP Trial: Intensive Control vs BP Trial: Standard Control: Stroke in the Blood Pressure Trial. | 36 of 2,363 62 of 2,371 | -1.1 points -1.9 to -0.3 | 4,734 | NCT00000620 Action to Control Cardiovascular Risk in Diabetes (ACCORD) |
| Pregnant Cohort vs Non-pregnant Cohort: Overall Survival | 39 of 659 570 of 4,073 | -8.1 points -10.0 to -5.8 | 4,732 | NCT03673306 Safety of Pregnancy in BRCA Mutated Breast Cancer Patients |
| Pregnant Cohort vs Non-pregnant Cohort: Breast Cancer-Specific Survival | 35 of 659 523 of 4,073 | -7.5 points -9.3 to -5.3 | 4,732 | NCT03673306 Safety of Pregnancy in BRCA Mutated Breast Cancer Patients |
| Pregnancy Cohort vs No Pregnancy Cohort: deaths from any cause | 39 of 659 570 of 4,073 | -8.1 points -10.0 to -5.8 | 4,732 | NCT03673306 Safety of Pregnancy in BRCA Mutated Breast Cancer Patients |
| NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe Acute Gastroenteritis (AGE) Occurring for >7 Days After Dosing Due to GI.1 or GII.4 Norovirus Strains (Excluding Co-infection) | 1 of 2,355 5 of 2,357 | -0.2 points -0.5 to 0.1 | 4,712 | NCT02669121 Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults |
| NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe AGE Occurring >7 Days After Dosing Due to Any Norovirus Strain (Excluding Co-infection) | 10 of 2,355 26 of 2,357 | -0.7 points -1.2 to -0.2 | 4,712 | NCT02669121 Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults |
| NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe AGE Occurring >7 Days After Dosing Due to Any Norovirus Strain (Including Co-infection) | 10 of 2,355 26 of 2,357 | -0.7 points -1.2 to -0.2 | 4,712 | NCT02669121 Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults |
| NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: Number of Participants With Moderate or Severe AGE Occurring >7 Days After Dosing Due to GI.1 or GII.4 Norovirus Strains (Including Co-infection) | 1 of 2,355 5 of 2,357 | -0.2 points -0.5 to 0.1 | 4,712 | NCT02669121 Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults |
| NoV GI.1/GII.4 Bivalent VLP Vaccine vs Placebo: serious adverse events | 29 of 2,355 35 of 2,357 | -0.3 points -0.9 to 0.4 | 4,712 | NCT02669121 Efficacy and Immunogenicity of Norovirus GI.1/GII.4 Bivalent Virus-like Particle Vaccine in Adults |
| Early ART vs Deferred ART: AIDs or AIDs Related Death | 31 of 2,325 83 of 2,359 | -2.2 points -3.1 to -1.3 | 4,684 | NCT00867048 Strategic Timing of Antiretroviral Treatment |
| Early ART vs Deferred ART: Composite Endpoint of AIDS, Serious Non-AIDS Diagnoses, and All-cause Mortality | 133 of 2,325 215 of 2,359 | -3.4 points -4.9 to -1.9 | 4,684 | NCT00867048 Strategic Timing of Antiretroviral Treatment |
| Early ART vs Deferred ART: Death, All-cause Mortality | 66 of 2,325 85 of 2,359 | -0.8 points -1.8 to 0.3 | 4,684 | NCT00867048 Strategic Timing of Antiretroviral Treatment |
| Early ART vs Deferred ART: deaths from any cause | 66 of 2,325 85 of 2,359 | -0.8 points -1.8 to 0.3 | 4,684 | NCT00867048 Strategic Timing of Antiretroviral Treatment |
| Early ART vs Deferred ART: Specific Non-AIDS Diagnoses | 107 of 2,325 137 of 2,359 | -1.2 points -2.5 to 0.1 | 4,684 | NCT00867048 Strategic Timing of Antiretroviral Treatment |
| Early ART vs Deferred ART: serious adverse events | 428 of 2,325 500 of 2,359 | -2.8 points -5.1 to -0.5 | 4,684 | NCT00867048 Strategic Timing of Antiretroviral Treatment |
| AZD7442 vs Placebo: The Incidence of Participants Who Have a Post-treatment Response (Negative at Baseline to Positive at Any Time Post-baseline) for SARS-CoV-2 Nucleocapsid Antibodies. | 198 of 3,121 139 of 1,563 | -2.5 points -4.3 to -1.0 | 4,684 | NCT04625725 Phase III Double-blind, Placebo-controlled Study of AZD7442 for Pre-exposure Prophylaxis of COVID-19 in Adult. |
Code
curl "https://conductscience.org/api/comparisons/v1?page=95"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=95
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT02499679-f8678195",
"title": "MACE Events Within 90 Days Subject Whose FFRCT Was >0.80 vs MACE Events Within 90 Days. Patients With at Least One FFRCT Value ≤ 0.80: Percentage of Major Adverse Coronary Events (MACE) at 90 Days",
"summary": "0 of 1592 against 19 of 3145; risk difference -0.6 points, 95% interval -0.9 to -0.3; NCT02499679, Assessing Diagnostic Value of Non-invasive FFRCT in Coronary Care",
"record": "/library/comparisons/NCT02499679-f8678195",
"nct_id": "NCT02499679",
"kind": "outcome",
"participants": 4737,
"risk_difference": {
"value": -0.006041335453100159,
"lower": -0.009416812924593985,
"upper": -0.002800273844722289
},
"group_1": "0 of 1,592",
"group_2": "19 of 3,145",
"difference": "-0.6 points",
"interval": "-0.9 to -0.3",
"trial_title": "Assessing Diagnostic Value of Non-invasive FFRCT in Coronary Care"
},
{
"id": "NCT03036124-deaths",
"title": "Dapa 10mg vs Placebo: deaths from any cause",
"summary": "286 of 2368 against 333 of 2368; risk difference -2.0 points, 95% interval -3.9 to -0.1; NCT03036124, Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure",
"record": "/library/comparisons/NCT03036124-deaths",
"nct_id": "NCT03036124",
"kind": "deaths",
"participants": 4736,
"risk_difference": {
"value": -0.01984797297297297,
"lower": -0.03906568896172795,
"upper": -0.000639261112046513
},
"group_1": "286 of 2,368",
"group_2": "333 of 2,368",
"difference": "-2.0 points",
"interval": "-3.9 to -0.1",
"trial_title": "Study to Evaluate the Effect of Dapagliflozin on the Incidence of Worsening Heart Failure or Cardiovascular Death in Patients With Chronic Heart Failure"
}
],
"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=96",
"request_id": "YRhv6HrmTKXlkiZa"
}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
Paste a sequence and see the patents that disclose it.
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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