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 last4,001 to 4,020 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Sulopenem-etzadroxil/Probenecid vs Ciprofloxacin: serious adverse events | 6 of 833 2 of 827 | 0.5 points -0.3 to 1.3 | 1,660 | NCT03354598 Oral Sulopenem-etzadroxil/Probenecid Versus Ciprofloxacin for Uncomplicated Urinary Tract Infection in Adult Women |
| Intervention vs Control: Number of Participants With a Symptomatic Stone Event | 154 of 826 165 of 832 | -1.2 points -5.0 to 2.6 | 1,658 | NCT03244189 Prevention of Urinary Stones With Hydration |
| Intervention vs Control: Number of Participants With Symptomatic Stone Recurrence, Asymptomatic Stone Formation, or Increase of Existing Stone by ≥2 mm in Any Dimension | 232 of 826 236 of 832 | -0.3 points -4.6 to 4.1 | 1,658 | NCT03244189 Prevention of Urinary Stones With Hydration |
| Intervention vs Control: Number of Participants With Growth of Existing Stone by ≥ 2 mm in Any Dimension | 45 of 826 32 of 832 | 1.6 points -0.4 to 3.7 | 1,658 | NCT03244189 Prevention of Urinary Stones With Hydration |
| Intervention vs Control: Number of Participants With Asymptomatic Formation of New Stone | 82 of 826 83 of 832 | -0.0 points -2.9 to 2.9 | 1,658 | NCT03244189 Prevention of Urinary Stones With Hydration |
| Intervention vs Control: deaths from any cause | 0 of 826 2 of 832 | -0.2 points -0.9 to 0.3 | 1,658 | NCT03244189 Prevention of Urinary Stones With Hydration |
| Multi-Model Intensive Discharge Program vs Usual Care: Number of Patients With a Nonelective Readmission Within 30 Days of the Index Discharge Date | 107 of 978 78 of 679 | -0.5 points -3.7 to 2.5 | 1,657 | NCT02130570 Relative Patient Benefits of a Hospital-PCMH Collaboration Within an ACO to Improve Care Transitions |
| Procalcitonin (PCT) Group vs Usual Care Group: Antibiotic Prescription in Emergency Department(ED) | 282 of 826 321 of 830 | -4.5 points -9.1 to 0.1 | 1,656 | NCT02130986 Procalcitonin Antibiotic Consensus Trial (ProACT) |
| Procalcitonin (PCT) Group vs Usual Care Group: deaths from any cause | 16 of 826 10 of 830 | 0.7 points -0.5 to 2.0 | 1,656 | NCT02130986 Procalcitonin Antibiotic Consensus Trial (ProACT) |
| Procalcitonin (PCT) Group vs Usual Care Group: Number of Participants With Any Adverse Outcome | 96 of 826 109 of 830 | -1.5 points -4.7 to 1.7 | 1,656 | NCT02130986 Procalcitonin Antibiotic Consensus Trial (ProACT) |
| Procalcitonin (PCT) Group vs Usual Care Group: serious adverse events | 14 of 826 9 of 830 | 0.6 points -0.6 to 1.9 | 1,656 | NCT02130986 Procalcitonin Antibiotic Consensus Trial (ProACT) |
| Standard CPR vs ACD CPR Plus ITD: serious adverse events | 766 of 813 787 of 840 | 0.5 points -1.8 to 2.9 | 1,653 | NCT00189423 ResQ Trial: Impact of an ITD and Active Compression Decompression CPR on Survival From Out-of-Hospital Cardiac Arrest |
| Continue HAART vs Stop HAART: deaths from any cause | 2 of 827 4 of 825 | -0.2 points -1.0 to 0.5 | 1,652 | NCT00955968 IMPAACT 1077HS: Examining Benefits of HAART Continuation in Postpartum Women |
| Continue HAART vs Stop HAART: serious adverse events | 10 of 827 3 of 825 | 0.8 points -0.0 to 1.9 | 1,652 | NCT00955968 IMPAACT 1077HS: Examining Benefits of HAART Continuation in Postpartum Women |
| Hydroxyprogesterone Caproate Injection, 250 mg/mL vs Vehicle: Stillbirths | 12 of 1,093 3 of 559 | 0.6 points -0.6 to 1.4 | 1,652 | NCT01004029 Confirmatory Study of 17P vs Vehicle for Prevention of Preterm Birth in Women w/ Previous Spontaneous Preterm Delivery |
| 17P (Hydroxyprogesterone Caproate Injection) vs Vehicle: Neonatal Composite Index (NCI) | 61 of 1,093 28 of 559 | 0.6 points -1.9 to 2.7 | 1,652 | NCT01004029 Confirmatory Study of 17P vs Vehicle for Prevention of Preterm Birth in Women w/ Previous Spontaneous Preterm Delivery |
| 17P (Hydroxyprogesterone Caproate Injection) vs Vehicle: Neonatal Deaths With ≥24 Weeks Gestational Age | 3 of 1,093 2 of 558 | -0.1 points -1.0 to 0.5 | 1,651 | NCT01004029 Confirmatory Study of 17P vs Vehicle for Prevention of Preterm Birth in Women w/ Previous Spontaneous Preterm Delivery |
| QuickOpt (Treatment) vs Control: All-cause, Cardiovascular and Heart Failure Mortality; | 44 of 816 42 of 828 | 0.3 points -1.9 to 2.5 | 1,644 | NCT00418314 FREEDOM - A Frequent Optimization Study Using the QuickOpt Method |
| QuickOpt (Treatment) vs Control: All Cause, Cardiovascular and Heart Failure Hospitalization | 294 of 816 303 of 828 | -0.6 points -5.2 to 4.1 | 1,644 | NCT00418314 FREEDOM - A Frequent Optimization Study Using the QuickOpt Method |
| QuickOpt (Treatment) vs Control: serious adverse events | 120 of 816 111 of 828 | 1.3 points -2.1 to 4.7 | 1,644 | NCT00418314 FREEDOM - A Frequent Optimization Study Using the QuickOpt Method |
Code
curl "https://conductscience.org/api/comparisons/v1?page=201"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=201
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT03354598-sae",
"title": "Sulopenem-etzadroxil/Probenecid vs Ciprofloxacin: serious adverse events",
"summary": "6 of 833 against 2 of 827; risk difference 0.5 points, 95% interval -0.3 to 1.3; NCT03354598, Oral Sulopenem-etzadroxil/Probenecid Versus Ciprofloxacin for Uncomplicated Urinary Tract Infection in Adult Women",
"record": "/library/comparisons/NCT03354598-sae",
"nct_id": "NCT03354598",
"kind": "serious-adverse-events",
"participants": 1660,
"risk_difference": {
"value": 0.004784501466850343,
"lower": -0.002671525568004025,
"upper": 0.013387373281045738
},
"group_1": "6 of 833",
"group_2": "2 of 827",
"difference": "0.5 points",
"interval": "-0.3 to 1.3",
"trial_title": "Oral Sulopenem-etzadroxil/Probenecid Versus Ciprofloxacin for Uncomplicated Urinary Tract Infection in Adult Women"
},
{
"id": "NCT03244189-354c2f44",
"title": "Intervention vs Control: Number of Participants With a Symptomatic Stone Event",
"summary": "154 of 826 against 165 of 832; risk difference -1.2 points, 95% interval -5.0 to 2.6; NCT03244189, Prevention of Urinary Stones With Hydration",
"record": "/library/comparisons/NCT03244189-354c2f44",
"nct_id": "NCT03244189",
"kind": "outcome",
"participants": 1658,
"risk_difference": {
"value": -0.011876629726205984,
"lower": -0.04980974062359413,
"upper": 0.02610872539733035
},
"group_1": "154 of 826",
"group_2": "165 of 832",
"difference": "-1.2 points",
"interval": "-5.0 to 2.6",
"trial_title": "Prevention of Urinary Stones With Hydration"
}
],
"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=202",
"request_id": "14EqDV1eLyJghXvs"
}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
Ask an assistant