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 last2,141 to 2,160 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Part B (Blinded): mRNA-1273 at Month 6 vs Part B (Blinded): mRNA-1273.222 at Month 6: Part B: Number of Participants With a First Occurrence of CDC-based COVID-19 Starting 14 Days After Month 6 Dose Until End of Follow up in RM6 Cohort Between Month 6 Monovalent and Bivalent Boost Groups | 151 of 1,976 142 of 2,012 | 0.6 points -1.0 to 2.2 | 3,988 | NCT05168813 Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern |
| Part B (Blinded): mRNA-1273 at Month 6 vs Part B (Blinded): mRNA-1273.222 at Month 6: Part B: Number of Participants With a First Occurrence of COVE-based Severe COVID-19 Starting 14 Days After Month 6 Dose Until End of Follow up in RM6 Cohort Between Month 6 Monovalent and Bivalent Groups | 1 of 1,976 0 of 2,012 | 0.1 points -0.1 to 0.3 | 3,988 | NCT05168813 Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern |
| Part B (Blinded): mRNA-1273 at Month 6 vs Part B (Blinded): mRNA-1273.222 at Month 6: Part B: Number of Participants With a First Occurrence of COVE-based COVID-19 Starting 14 Days After Month 6 Dose Until End of Follow up in RM6 Cohort Between Month 6 Monovalent and Bivalent Boost Group | 8 of 1,976 7 of 2,012 | 0.1 points -0.4 to 0.5 | 3,988 | NCT05168813 Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern |
| Telcagepant 140 mg vs Placebo: Number of Participants With Clinical Adverse Events (AEs) | 1,582 of 2,660 804 of 1,326 | -1.2 points -4.4 to 2.1 | 3,986 | NCT01125774 Telcagepant for Prevention of Menstrually Related Migraine in Female Participants With Episodic Migraine (MK-0974-065) |
| Telcagepant 140 mg vs Placebo: Number of Participants Who Discontinued Study Due to a Clinical AE | 66 of 2,660 36 of 1,326 | -0.2 points -1.4 to 0.8 | 3,986 | NCT01125774 Telcagepant for Prevention of Menstrually Related Migraine in Female Participants With Episodic Migraine (MK-0974-065) |
| Telcagepant 140 mg vs Placebo: serious adverse events | 25 of 2,660 10 of 1,326 | 0.2 points -0.5 to 0.7 | 3,986 | NCT01125774 Telcagepant for Prevention of Menstrually Related Migraine in Female Participants With Episodic Migraine (MK-0974-065) |
| Active Antihypertensive Treatment vs Usual Care: Recurrent Stroke | 28 of 1,988 43 of 1,987 | -0.8 points -1.6 to 0.1 | 3,975 | NCT01840072 China Antihypertensive Trial in Acute Ischemic Stroke |
| Active Antihypertensive Treatment vs Usual Care: Other Vascular Events | 48 of 1,988 59 of 1,987 | -0.6 points -1.6 to 0.5 | 3,975 | NCT01840072 China Antihypertensive Trial in Acute Ischemic Stroke |
| Active Antihypertensive Treatment vs Usual Care: Mortality | 68 of 1,988 54 of 1,987 | 0.7 points -0.4 to 1.8 | 3,975 | NCT01840072 China Antihypertensive Trial in Acute Ischemic Stroke |
| Active Antihypertensive Treatment vs Usual Care: A Combination of All-cause Mortality and Major Disability at the 3-month Post-treatment Follow-up. | 500 of 1,988 502 of 1,987 | -0.1 points -2.8 to 2.6 | 3,975 | NCT01840072 China Antihypertensive Trial in Acute Ischemic Stroke |
| Tiotropium vs Placebo: serious adverse events | 342 of 1,952 336 of 1,965 | 0.4 points -1.9 to 2.8 | 3,917 | NCT00387088 Tiotropium / Respimat One Year Study in COPD. |
| Telcagepant 140 mg vs Placebo: Number of Participants With Laboratory AEs | 76 of 2,610 30 of 1,305 | 0.6 points -0.5 to 1.6 | 3,915 | NCT01125774 Telcagepant for Prevention of Menstrually Related Migraine in Female Participants With Episodic Migraine (MK-0974-065) |
| Telcagepant 140 mg vs Placebo: Number of Participants Who Discontinued Study Due to a Laboratory AE | 8 of 2,610 2 of 1,305 | 0.2 points -0.3 to 0.5 | 3,915 | NCT01125774 Telcagepant for Prevention of Menstrually Related Migraine in Female Participants With Episodic Migraine (MK-0974-065) |
| EBQI-Supported WH-PACT Implementation vs Routine WH-PACT Implementation: deaths from any cause | 5 of 2,720 3 of 1,180 | -0.1 points -0.6 to 0.2 | 3,900 | NCT02039856 Implementation of Women's Health Patient Aligned Care Teams |
| Tiotropium vs Placebo: Number of Patients With at Least One Hospitalisation for a COPD Exacerbation | 161 of 1,939 198 of 1,953 | -1.8 points -3.7 to -0.0 | 3,892 | NCT00387088 Tiotropium / Respimat One Year Study in COPD. |
| Tiotropium vs Placebo: Number of Patients With at Least One COPD Exacerbation | 685 of 1,939 842 of 1,953 | -7.8 points -10.8 to -4.7 | 3,892 | NCT00387088 Tiotropium / Respimat One Year Study in COPD. |
| Letrozole vs Placebo: serious adverse events | 80 of 1,951 87 of 1,938 | -0.4 points -1.7 to 0.9 | 3,889 | NCT00382070 Letrozole in Treating Postmenopausal Women Who Have Received Hormone Therapy for Hormone Receptor-Positive Breast Cancer |
| Group 1: Ad26.Mos4.HIV + Clade C and Mosaic gp140 vs Group 2: Placebo: Number of Participants With Serious Adverse Events (SAEs) | 82 of 1,942 77 of 1,945 | 0.3 points -1.0 to 1.5 | 3,887 | NCT03964415 A Study of Heterologous Vaccine Regimen of Adenovirus Serotype 26 Mosaic4 Human Immunodeficiency Virus(Ad26.Mos4.HIV), Adjuvanted Clade C gp140 and Mosaic gp140 to Prevent HIV-1 Infection Among Cis-gender Men and Transgender Individuals Who Have Sex With Cis-gender Men and/or Transgender Individuals |
| Group 1: Ad26.Mos4.HIV + Clade C and Mosaic gp140 vs Group 2: Placebo: Number of Participants With Medically-attended Adverse Events (MAAEs) | 999 of 1,942 1,002 of 1,945 | -0.1 points -3.2 to 3.1 | 3,887 | NCT03964415 A Study of Heterologous Vaccine Regimen of Adenovirus Serotype 26 Mosaic4 Human Immunodeficiency Virus(Ad26.Mos4.HIV), Adjuvanted Clade C gp140 and Mosaic gp140 to Prevent HIV-1 Infection Among Cis-gender Men and Transgender Individuals Who Have Sex With Cis-gender Men and/or Transgender Individuals |
| Group 1: Ad26.Mos4.HIV + Clade C and Mosaic gp140 vs Group 2: Placebo: Number of Participants Who Discontinued the Study or Study Intervention Due to Adverse Events (AEs) | 11 of 1,942 16 of 1,945 | -0.3 points -0.8 to 0.3 | 3,887 | NCT03964415 A Study of Heterologous Vaccine Regimen of Adenovirus Serotype 26 Mosaic4 Human Immunodeficiency Virus(Ad26.Mos4.HIV), Adjuvanted Clade C gp140 and Mosaic gp140 to Prevent HIV-1 Infection Among Cis-gender Men and Transgender Individuals Who Have Sex With Cis-gender Men and/or Transgender Individuals |
Code
curl "https://conductscience.org/api/comparisons/v1?page=108"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=108
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT05168813-1bc0a9aa",
"title": "Part B (Blinded): mRNA-1273 at Month 6 vs Part B (Blinded): mRNA-1273.222 at Month 6: Part B: Number of Participants With a First Occurrence of CDC-based COVID-19 Starting 14 Days After Month 6 Dose Until End of Follow up in RM6 Cohort Between Month 6 Monovalent and Bivalent Boost Groups",
"summary": "151 of 1976 against 142 of 2012; risk difference 0.6 points, 95% interval -1.0 to 2.2; NCT05168813, Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern",
"record": "/library/comparisons/NCT05168813-1bc0a9aa",
"nct_id": "NCT05168813",
"kind": "outcome",
"participants": 3988,
"risk_difference": {
"value": 0.0058404632931158,
"lower": -0.010398267347622156,
"upper": 0.022136695903160374
},
"group_1": "151 of 1,976",
"group_2": "142 of 2,012",
"difference": "0.6 points",
"interval": "-1.0 to 2.2",
"trial_title": "Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern"
},
{
"id": "NCT05168813-774041bd",
"title": "Part B (Blinded): mRNA-1273 at Month 6 vs Part B (Blinded): mRNA-1273.222 at Month 6: Part B: Number of Participants With a First Occurrence of COVE-based Severe COVID-19 Starting 14 Days After Month 6 Dose Until End of Follow up in RM6 Cohort Between Month 6 Monovalent and Bivalent Groups",
"summary": "1 of 1976 against 0 of 2012; risk difference 0.1 points, 95% interval -0.1 to 0.3; NCT05168813, Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern",
"record": "/library/comparisons/NCT05168813-774041bd",
"nct_id": "NCT05168813",
"kind": "outcome",
"participants": 3988,
"risk_difference": {
"value": 0.0005060728744939271,
"lower": -0.001444596914272216,
"upper": 0.002861128099984624
},
"group_1": "1 of 1,976",
"group_2": "0 of 2,012",
"difference": "0.1 points",
"interval": "-0.1 to 0.3",
"trial_title": "Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern"
}
],
"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=109",
"request_id": "6a8SuAd_rLqJ7fap"
}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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