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 last4,801 to 4,820 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Liquid Rotarix Group vs Lyophilized Rotarix Group: serious adverse events | 37 of 636 38 of 638 | -0.1 points -2.8 to 2.5 | 1,274 | NCT00363545 To Assess Immunogenicity, Reactogenicity & Safety of 2 Formulations of GSK's HRV Vaccine as 2-dose Vaccination (Infants) |
| 38 Weeks Group vs 39 Weeks Group: serious adverse events | 1 of 636 2 of 638 | -0.2 points -1.0 to 0.6 | 1,274 | NCT00835003 Timing of Planned Caesarean Section and Morbidity of the Newborn |
| PA Group vs AL Group: serious adverse events | 3 of 849 2 of 423 | -0.1 points -1.4 to 0.6 | 1,272 | NCT00422084 Pyronaridine Artesunate (3:1) Versus Coartem® in P Falciparum Malaria Patients |
| 38 Weeks Group vs 39 Weeks Group: Neonatal Admission After Elective Caesarean Section | 88 of 635 76 of 637 | 1.9 points -1.8 to 5.6 | 1,272 | NCT00835003 Timing of Planned Caesarean Section and Morbidity of the Newborn |
| HRV Porcine Circovirus (PCV)-Free Liquid Group vs HRV Lyophilized Group: Number of Subjects With Any Serious Adverse Events (SAEs). | 20 of 632 19 of 640 | 0.2 points -1.8 to 2.2 | 1,272 | NCT03207750 This Study Will Evaluate the Immunogenicity, Reactogenicity and Safety of the Routine Infant Vaccines Pediarix®, Hiberix® and Prevenar 13® When Co-administered With GlaxoSmithKline (GSK) Biologicals' Liquid Human Rotavirus Vaccine (HRV) as Compared to GSK's Licensed Lyophilized Vaccine |
| HRV Porcine Circovirus (PCV)-Free Liquid Group vs HRV Lyophilized Group: deaths from any cause | 1 of 632 0 of 640 | 0.2 points -0.5 to 0.9 | 1,272 | NCT03207750 This Study Will Evaluate the Immunogenicity, Reactogenicity and Safety of the Routine Infant Vaccines Pediarix®, Hiberix® and Prevenar 13® When Co-administered With GlaxoSmithKline (GSK) Biologicals' Liquid Human Rotavirus Vaccine (HRV) as Compared to GSK's Licensed Lyophilized Vaccine |
| HRV Porcine Circovirus (PCV)-Free Liquid Group vs HRV Lyophilized Group: Number of Subjects With Any Unsolicited AEs. | 294 of 632 327 of 640 | -4.6 points -10.0 to 0.9 | 1,272 | NCT03207750 This Study Will Evaluate the Immunogenicity, Reactogenicity and Safety of the Routine Infant Vaccines Pediarix®, Hiberix® and Prevenar 13® When Co-administered With GlaxoSmithKline (GSK) Biologicals' Liquid Human Rotavirus Vaccine (HRV) as Compared to GSK's Licensed Lyophilized Vaccine |
| HRV Porcine Circovirus (PCV)-Free Liquid Group vs HRV Lyophilized Group: serious adverse events | 20 of 632 19 of 640 | 0.2 points -1.8 to 2.2 | 1,272 | NCT03207750 This Study Will Evaluate the Immunogenicity, Reactogenicity and Safety of the Routine Infant Vaccines Pediarix®, Hiberix® and Prevenar 13® When Co-administered With GlaxoSmithKline (GSK) Biologicals' Liquid Human Rotavirus Vaccine (HRV) as Compared to GSK's Licensed Lyophilized Vaccine |
| Pyronaridine - Artesunate vs Mefloquine Plus Artesunate: serious adverse events | 6 of 848 3 of 423 | -0.0 points -1.4 to 0.9 | 1,271 | NCT00403260 Pyronaridine - Artesunate (3:1) Versus Mefloquine Plus Artesunate in Plasmodium Falciparum Malaria Patients |
| Testosterone vs Placebo: serious adverse events | 33 of 1,019 10 of 251 | -0.7 points -4.1 to 1.5 | 1,270 | NCT00467259 Endometrial Safety Study of Transdermal Testosterone (300 Mcg/Day) in Naturally Postmenopausal Women |
| IVR Intervention Group vs IVR Control Group: serious adverse events | 138 of 604 149 of 666 | 0.5 points -4.1 to 5.1 | 1,270 | NCT02056431 Balancing Treatment Outcomes and Medication Burden Among Patients With Symptomatic Diabetic Peripheral Neuropathy |
| Best Practice Clinic-Based Care vs Telehealth Care: Number of Participants Reporting High Confidence in Reporting Contacting Care Team at Six Months Confidence in Managing Blood Pressure: Contact Care Team | 481 of 671 467 of 598 | -6.4 points -11.1 to -1.6 | 1,269 | NCT02996565 Pragmatic Trial Comparing Telehealth Care and Optimized Clinic-Based Care for Uncontrolled High Blood Pressure |
| Best Practice Clinic-Based Care vs Telehealth Care: Number of Participants Reporting High Confidence in Keeping BP Below Target at Six Months | 242 of 670 252 of 599 | -6.0 points -11.3 to -0.6 | 1,269 | NCT02996565 Pragmatic Trial Comparing Telehealth Care and Optimized Clinic-Based Care for Uncontrolled High Blood Pressure |
| Chemotherapy Cohort vs Hormonal Therapy Cohort: serious adverse events | 76 of 832 22 of 435 | 4.1 points 1.0 to 6.8 | 1,267 | NCT00726661 An Observational Study of Treatment Patterns and Safety Outcomes for Metastatic or Locally Recurrent Breast Cancer (VIRGO) |
| Afluria® Group vs Fluzone® Group: serious adverse events | 22 of 630 26 of 636 | -0.6 points -2.8 to 1.6 | 1,266 | NCT00735475 A Study to Determine the Immunogenicity and Safety Profile of CSL Limited's Influenza Virus Vaccine Compared to a US Licensed Comparator Influenza Virus Vaccine |
| Cervarix Group Without HPV-18 12-Month Persistent Infection vs Cervarix Group With HPV-18 12-Month Persistent Infection: Number of Seroconverted Subjects for Anti-HPV-18 Without and With 12-month Persistent Infection | 1,237 of 1,243 21 of 21 | -0.5 points -1.0 to 15.0 | 1,264 | NCT00122681 Human Papilloma Virus (HPV) Vaccine Efficacy Trial Against Cervical Pre-cancer in Young Adults With GlaxoSmithKline (GSK) Biologicals HPV-16/18 |
| Molnupiravir vs Placebo: Percentage of Participants Who Had Undetectable SARS-CoV-2 in Baseline NP Swabs and Developed COVID-19 (Laboratory-Confirmed SARS-CoV-2 Infection With Symptoms) Through Day 29 | 51 of 630 65 of 634 | -2.2 points -5.4 to 1.0 | 1,264 | NCT04939428 Study of MK-4482 for Prevention of Coronavirus Disease 2019 (COVID-19) in Adults (MK-4482-013) |
| TAXUS Element vs TAXUS Express: serious adverse events | 334 of 942 110 of 320 | 1.1 points -5.1 to 7.0 | 1,262 | NCT00484315 TAXUS PERSEUS Workhorse |
| Regional Anesthesia vs General Anesthesia: Postoperative Delirium | 130 of 633 124 of 629 | 0.8 points -3.6 to 5.2 | 1,262 | NCT02507505 Regional Versus General Anesthesia for Promoting Independence After Hip Fracture |
| Best Practice Clinic-Based Care vs Telehealth Care: Number of Participants Reporting High Confidence in Taking BP Medications at Six Months | 564 of 667 532 of 595 | -4.9 points -8.5 to -1.1 | 1,262 | NCT02996565 Pragmatic Trial Comparing Telehealth Care and Optimized Clinic-Based Care for Uncontrolled High Blood Pressure |
Code
curl "https://conductscience.org/api/comparisons/v1?page=241"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=241
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00363545-sae",
"title": "Liquid Rotarix Group vs Lyophilized Rotarix Group: serious adverse events",
"summary": "37 of 636 against 38 of 638; risk difference -0.1 points, 95% interval -2.8 to 2.5; NCT00363545, To Assess Immunogenicity, Reactogenicity & Safety of 2 Formulations of GSK's HRV Vaccine as 2-dose Vaccination (Infants)",
"record": "/library/comparisons/NCT00363545-sae",
"nct_id": "NCT00363545",
"kind": "serious-adverse-events",
"participants": 1274,
"risk_difference": {
"value": -0.001385027897714948,
"lower": -0.02769950838529791,
"upper": 0.024918780938716377
},
"group_1": "37 of 636",
"group_2": "38 of 638",
"difference": "-0.1 points",
"interval": "-2.8 to 2.5",
"trial_title": "To Assess Immunogenicity, Reactogenicity & Safety of 2 Formulations of GSK's HRV Vaccine as 2-dose Vaccination (Infants)"
},
{
"id": "NCT00835003-sae",
"title": "38 Weeks Group vs 39 Weeks Group: serious adverse events",
"summary": "1 of 636 against 2 of 638; risk difference -0.2 points, 95% interval -1.0 to 0.6; NCT00835003, Timing of Planned Caesarean Section and Morbidity of the Newborn",
"record": "/library/comparisons/NCT00835003-sae",
"nct_id": "NCT00835003",
"kind": "serious-adverse-events",
"participants": 1274,
"risk_difference": {
"value": -0.0015624691942193567,
"lower": -0.009886017334049422,
"upper": 0.006064254992967399
},
"group_1": "1 of 636",
"group_2": "2 of 638",
"difference": "-0.2 points",
"interval": "-1.0 to 0.6",
"trial_title": "Timing of Planned Caesarean Section and Morbidity of the Newborn"
}
],
"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"
},
{
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"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=242",
"request_id": "izWDh22KRAOGiFVT"
}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.
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GET https://conductscience.org/api/comparisons/v1?q=placebo%20heart%20failure&kind=outcome
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