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 last2,101 to 2,120 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Vaccine vs Placebo: Number of Participants With Wild Type-4 Febrile Adenovirus (ADV) Acute Respiratory Disease (ARD) -- ITT Cohort | 1 of 3,031 48 of 1,009 | -4.7 points -6.2 to -3.6 | 4,040 | NCT00382408 A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001 |
| Vaccine vs Placebo: Number of Participants With Wild Type-4 Adenovirus (ADV) Acute Respiratory Disease (ARD) -- ITT Cohort | 3 of 3,031 65 of 1,009 | -6.3 points -8.0 to -5.0 | 4,040 | NCT00382408 A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001 |
| Vaccine vs Placebo: Number of Participants With Wild Type-4 Febrile Adenovirus (ADV) Acute Respiratory Disease (ARD) -- ITT Cohort --- Day 11-56 | 0 of 3,031 44 of 1,009 | -4.4 points -5.8 to -3.3 | 4,040 | NCT00382408 A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001 |
| Vaccine vs Placebo: serious adverse events | 35 of 3,031 12 of 1,009 | -0.0 points -1.0 to 0.6 | 4,040 | NCT00382408 A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001 |
| Darbepoetin Alfa vs Placebo: Time to Cardiovascular Mortality | 259 of 2,012 250 of 2,026 | 0.5 points -1.5 to 2.6 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to Cerebrovascular Accident | 101 of 2,012 53 of 2,026 | 2.4 points 1.2 to 3.6 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to All-cause Mortality or Cardiovascular (CV) Events Including Hospitalization Due to Acute Myocardial Ischemia, Congestive Heart Failure (CHF), Myocardial Infarction (MI), and Cerebrovascular Accident (CVA) | 632 of 2,012 602 of 2,026 | 1.7 points -1.1 to 4.5 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to Congestive Heart Failure | 205 of 2,012 229 of 2,026 | -1.1 points -3.0 to 0.8 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to Myocardial Infarction | 124 of 2,012 129 of 2,026 | -0.2 points -1.7 to 1.3 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to All-cause Mortality | 412 of 2,012 395 of 2,026 | 1.0 points -1.5 to 3.4 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to Hospitalization Due to Acute Myocardial Ischemia | 41 of 2,012 49 of 2,026 | -0.4 points -1.3 to 0.5 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to All-cause Mortality or End Stage Renal Disease (ESRD) | 652 of 2,012 618 of 2,026 | 1.9 points -1.0 to 4.8 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Darbepoetin Alfa vs Placebo: Time to End Stage Renal Disease | 338 of 2,012 330 of 2,026 | 0.5 points -1.8 to 2.8 | 4,038 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| V260 With Staggered or Concomitant EPI vs Placebo With Staggered or Concomitant EPI: serious adverse events | 339 of 2,015 338 of 2,019 | 0.1 points -2.2 to 2.4 | 4,034 | NCT02062385 Efficacy, Safety, and Immunogenicity of V260 in Healthy Chinese Infants (V260-024) |
| rIL-2 vs No rIL-2: Pattern of Use of Prophylaxis for Opportunistic Infections | 54 of 2,028 53 of 2,005 | 0.0 points -1.0 to 1.0 | 4,033 | NCT00004978 An International Study to Evaluate Recombinant Interleukin-2 in HIV Positive Patients Taking Anti-retroviral Therapy |
| Non Pre-treatment vs Pre-treatment: serious adverse events | 167 of 1,996 206 of 2,037 | -1.7 points -3.5 to 0.0 | 4,033 | NCT01015287 A Comparison of Prasugrel at PCI or Time of Diagnosis of Non-ST Elevation Myocardial Infarction |
| Darbepoetin Alfa vs Placebo: serious adverse events | 1,235 of 2,004 1,219 of 2,019 | 1.3 points -1.8 to 4.3 | 4,023 | NCT00093015 Trial to Reduce Cardiovascular Events With Aranesp® Therapy (TREAT) |
| Menhibrix Group vs ActHIB Group: serious adverse events | 72 of 3,010 18 of 1,010 | 0.6 points -0.5 to 1.5 | 4,020 | NCT00345683 Safety of Hib-MenCY-TT Vaccine Versus Licensed Hib Conjugate Vaccine, Given at 12 to 15 Months of Age. |
| Dapa 10 mg vs Placebo: deaths from any cause | 41 of 2,019 33 of 1,998 | 0.4 points -0.5 to 1.2 | 4,017 | NCT04564742 Dapagliflozin Effects on Cardiometabolic Outcomes in Patients With an Acute Heart Attack. |
| Dapa 10 mg vs Placebo: serious adverse events | 449 of 2,019 404 of 1,998 | 2.0 points -0.5 to 4.5 | 4,017 | NCT04564742 Dapagliflozin Effects on Cardiometabolic Outcomes in Patients With an Acute Heart Attack. |
Code
curl "https://conductscience.org/api/comparisons/v1?page=106"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=106
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00382408-3b51d6a4",
"title": "Vaccine vs Placebo: Number of Participants With Wild Type-4 Febrile Adenovirus (ADV) Acute Respiratory Disease (ARD) -- ITT Cohort",
"summary": "1 of 3031 against 48 of 1009; risk difference -4.7 points, 95% interval -6.2 to -3.6; NCT00382408, A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001",
"record": "/library/comparisons/NCT00382408-3b51d6a4",
"nct_id": "NCT00382408",
"kind": "outcome",
"participants": 4040,
"risk_difference": {
"value": -0.04724192920266594,
"lower": -0.062181147419366437,
"upper": -0.035634913513861
},
"group_1": "1 of 3,031",
"group_2": "48 of 1,009",
"difference": "-4.7 points",
"interval": "-6.2 to -3.6",
"trial_title": "A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001"
},
{
"id": "NCT00382408-84f8f823",
"title": "Vaccine vs Placebo: Number of Participants With Wild Type-4 Adenovirus (ADV) Acute Respiratory Disease (ARD) -- ITT Cohort",
"summary": "3 of 3031 against 65 of 1009; risk difference -6.3 points, 95% interval -8.0 to -5.0; NCT00382408, A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001",
"record": "/library/comparisons/NCT00382408-84f8f823",
"nct_id": "NCT00382408",
"kind": "outcome",
"participants": 4040,
"risk_difference": {
"value": -0.0634304456853021,
"lower": -0.08030432884663094,
"upper": -0.04973852432938587
},
"group_1": "3 of 3,031",
"group_2": "65 of 1,009",
"difference": "-6.3 points",
"interval": "-8.0 to -5.0",
"trial_title": "A Clinical Trial to Evaluate the Safety, Efficacy, and Immunogenicity of DR-5001"
}
],
"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=107",
"request_id": "flG0cqQusScXW81P"
}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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