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One gene with its proteins, patents, drugs, trials, grants and papers.
85,013 comparisons from ClinicalTrials.gov. Counted 2026-11-10.
Most participants first33,758 with no events in either group come last201 to 220 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase) | 575 of 21,898 1,189 of 21,890 | -2.8 points -3.2 to -2.4 | 43,788 | NCT04505722 A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants |
| Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Medically-Attended Adverse Events (MAAEs) (Double Blind Phase) | 1,672 of 21,894 1,885 of 21,882 | -1.0 points -1.5 to -0.5 | 43,776 | NCT04505722 A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants |
| Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Adverse Events of Special Interest (AESI) (Double Blind Phase) | 6 of 21,894 5 of 21,882 | 0.0 points -0.0 to 0.0 | 43,776 | NCT04505722 A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants |
| Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With MAAEs Leading to Study Discontinuation (Double Blind Phase) | 1 of 21,894 2 of 21,882 | -0.0 points -0.0 to 0.0 | 43,776 | NCT04505722 A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants |
| Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Serious Adverse Events (SAEs) (Double Blind Phase) | 235 of 21,894 358 of 21,882 | -0.6 points -0.8 to -0.3 | 43,776 | NCT04505722 A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants |
| FluNG Group vs Fluarix Group: serious adverse events | 4,071 of 21,893 4,066 of 21,802 | -0.1 points -0.8 to 0.7 | 43,695 | NCT00753272 Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older |
| FluNG Group vs Fluarix Group: Number of Subjects Reporting Polymerase Chain Reaction (PCR)-Confirmed Influenza A and/or B Infection. | 274 of 21,573 310 of 21,482 | -0.2 points -0.4 to 0.0 | 43,055 | NCT00753272 Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older |
| Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase) | 487 of 21,537 1,079 of 21,467 | -2.8 points -3.1 to -2.4 | 43,004 | NCT04505722 A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants |
| FluNG Group vs Fluarix Group: Number of Subjects Reporting All-cause Death After the First Dose of Vaccine. | 63 of 21,394 88 of 21,337 | -0.1 points -0.2 to -0.0 | 42,731 | NCT00753272 Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older |
| FluNG Group vs Fluarix Group: Number of Subjects Reporting Hospitalization Due to Respiratory Diseases After the First Dose of Vaccine | 84 of 21,394 89 of 21,337 | -0.0 points -0.1 to 0.1 | 42,731 | NCT00753272 Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older |
| FluNG Group vs Fluarix Group: Number of Subjects Reporting Pneumonia or Clinical Influenza After the First Dose of Vaccine. | 202 of 21,394 225 of 21,337 | -0.1 points -0.3 to 0.1 | 42,731 | NCT00753272 Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older |
| Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase) | 436 of 21,244 895 of 20,978 | -2.2 points -2.5 to -1.9 | 42,222 | NCT04505722 A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants |
| EHR-facilitated Collaborative Care (Intervention) vs Usual Care (Control): Number of Deceased Participants | 3,192 of 24,874 2,214 of 16,180 | -0.9 points -1.5 to -0.2 | 41,054 | NCT03892967 Enhanced, EHR-facilitated Cancer Symptom Control Pragmatic Clinical Trial |
| EHR-facilitated Collaborative Care (Intervention) vs Usual Care (Control): deaths from any cause | 3,192 of 24,874 2,214 of 16,180 | -0.9 points -1.5 to -0.2 | 41,054 | NCT03892967 Enhanced, EHR-facilitated Cancer Symptom Control Pragmatic Clinical Trial |
| FluNG Group vs Fluarix Group: Number of Subjects Reporting Polymerase Chain Reaction (PCR)-Confirmed Influenza A and/or B Infection. | 262 of 20,579 296 of 20,458 | -0.2 points -0.4 to 0.1 | 41,037 | NCT00753272 Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older |
| FluNG Group vs Fluarix Group: Number of Subjects Reporting Culture-confirmed Influenza A and/or B Infection. | 144 of 20,579 145 of 20,458 | -0.0 points -0.2 to 0.2 | 41,037 | NCT00753272 Trial to Evaluate the Efficacy of GSK Biologicals' Influenza Vaccine GSK2186877A in Adults 65 Year of Age and Older |
| Matched Treated: Long-term Disability vs Matched Untreated: Long-term Disability: Number of Participants With Any Long Term Disability (LTD) Claim: Matched Participants | 50 of 20,318 74 of 20,318 | -0.1 points -0.2 to -0.0 | 40,636 | NCT07072793 A US Study to Look at Loss of Work and Healthcare Costs for People Affected With Mild-to-moderate COVID 19 Who Have High Chances of the Disease Becoming Severe |
| Female Cases vs Female Controls: Number of New Onset Skin Cancers in the Female Sex Subgroup | 78 of 8,159 429 of 32,121 | -0.4 points -0.6 to -0.1 | 40,280 | NCT04969419 Incidence of Melanoma and Non-melanoma Skin Cancer in People With Vitiligo |
| Matched Treated: Short-term Disability vs Matched Untreated: Short-term Disability: Number of Participants With Any Short Term Disability (STD) Claim: Matched Participants | 1,343 of 20,065 1,848 of 20,065 | -2.5 points -3.0 to -2.0 | 40,130 | NCT07072793 A US Study to Look at Loss of Work and Healthcare Costs for People Affected With Mild-to-moderate COVID 19 Who Have High Chances of the Disease Becoming Severe |
| eSyM Control Participants (Medical Oncology and Surgery Participants Combined) vs eSyM Intervention Participants (Medical Oncology and Surgery Participants Combined): deaths from any cause | 4,898 of 21,112 4,161 of 18,830 | 1.1 points 0.3 to 1.9 | 39,942 | NCT03850912 Symptom Management Implementation of Patient Reported Outcomes in Oncology |
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=11
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"id": "NCT04505722-e20eadc8",
"title": "Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With First Occurrence of Molecularly Confirmed Moderate to Severe/Critical COVID-19 Regardless of Their Serostatus (Double Blind Phase)",
"summary": "575 of 21898 against 1189 of 21890; risk difference -2.8 points, 95% interval -3.2 to -2.4; NCT04505722, A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants",
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{
"id": "NCT04505722-89e40f6c",
"title": "Double-blind Phase: Ad26.COV2.S 5*10^10 vp vs Double-blind Phase: Placebo: Number of Participants With Medically-Attended Adverse Events (MAAEs) (Double Blind Phase)",
"summary": "1672 of 21894 against 1885 of 21882; risk difference -1.0 points, 95% interval -1.5 to -0.5; NCT04505722, A Study of Ad26.COV2.S for the Prevention of SARS-CoV-2-Mediated COVID-19 in Adult Participants",
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}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.
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Patent publications
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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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