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85,013 comparisons from ClinicalTrials.gov. Counted 2026-11-10.
Most participants first33,758 with no events in either group come last1,201 to 1,220 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| S-268019-b vs Placebo: Number of Participants With First Occurrence of SARS-CoV-2 RT-PCR-Positive Severe COVID-19 in the Initial Vaccination Period With Onset at Least 14 Days Following Second Vaccination | 0 of 5,181 1 of 2,617 | -0.0 points -0.2 to 0.0 | 7,798 | NCT05212948 A Study of S-268019 for the Prevention of COVID-19 |
| Male vs Female: Risk Factors for the Proportion of Responders of Tolterodine-Gender | 2,745 of 3,394 3,791 of 4,386 | -5.6 points -7.2 to -3.9 | 7,780 | NCT01488578 Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan) |
| With Non-drug Therapies vs Without Non-drug Therapies: Risk Factors for the Proportion of Responders of Tolterodine-Non-drug Therapies | 317 of 360 6,219 of 7,420 | 4.2 points 0.4 to 7.3 | 7,780 | NCT01488578 Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan) |
| With Concomitant Drugs vs Without Concomitant Drugs: Risk Factors for the Proportion of Responders of Tolterodine-Concomitant Drugs | 3,483 of 4,214 3,053 of 3,566 | -3.0 points -4.6 to -1.3 | 7,780 | NCT01488578 Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan) |
| With Complications vs Without Complications: Risk Factors for the Proportion of Responders of Tolterodine-Complications | 3,960 of 4,806 2,576 of 2,974 | -4.2 points -5.8 to -2.6 | 7,780 | NCT01488578 Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan) |
| <65 Years vs >=65 Years: Risk Factors for the Proportion of Responders of Tolterodine-Age | 2,060 of 2,379 4,476 of 5,401 | 3.7 points 2.0 to 5.4 | 7,780 | NCT01488578 Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan) |
| No-intervention Control vs School-based Smoking Prevention Curriculum: Whether or Not Smoking Daily at 2 Years After High School | 1,132 of 3,894 1,103 of 3,881 | 0.6 points -1.4 to 2.7 | 7,775 | NCT00115869 Hutchinson Smoking Prevention Project |
| Pitavastatin vs Placebo: deaths from any cause | 126 of 3,888 143 of 3,881 | -0.4 points -1.3 to 0.4 | 7,769 | NCT02344290 Evaluating the Use of Pitavastatin to Reduce the Risk of Cardiovascular Disease in HIV-Infected Adults |
| Pitavastatin vs Placebo: serious adverse events | 750 of 3,888 755 of 3,881 | -0.2 points -1.9 to 1.6 | 7,769 | NCT02344290 Evaluating the Use of Pitavastatin to Reduce the Risk of Cardiovascular Disease in HIV-Infected Adults |
| Cangrelor Arm vs Clopidogrel Arm: Incidence of Abrupt Closure, Threatened Abrupt Closure, Need for Urgent Coronary Artery Bypass Graft (CABG) Surgery, or Unsuccessful Procedure During the Index PCI | 127 of 3,897 141 of 3,871 | -0.4 points -1.2 to 0.4 | 7,768 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Denosumab 60 mg Q6M vs Placebo: serious adverse events | 1,004 of 3,886 972 of 3,876 | 0.8 points -1.2 to 2.7 | 7,762 | NCT00089791 A Study to Evaluate Denosumab in the Treatment of Postmenopausal Osteoporosis |
| Cohort 2011 vs Cohort 2019: deaths from any cause | 591 of 4,753 157 of 3,002 | 7.2 points 6.0 to 8.4 | 7,755 | NCT03343886 Ageing and Health. Spanish Longitudinal Study |
| Cohort 2011 vs Cohort 2019: serious adverse events | 706 of 4,753 234 of 3,002 | 7.1 points 5.6 to 8.4 | 7,755 | NCT03343886 Ageing and Health. Spanish Longitudinal Study |
| Cangrelor Arm vs Clopidogrel Arm: Incidence of All-cause Mortality, Myocardial Infarction (MI), and Ischemia-driven Revascularization (IDR) | 290 of 3,889 276 of 3,865 | 0.3 points -0.8 to 1.5 | 7,754 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Cangrelor Arm vs Clopidogrel Arm: Individual Incidence of All-cause Mortality | 8 of 3,889 5 of 3,865 | 0.1 points -0.1 to 0.3 | 7,754 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Cangrelor Arm vs Clopidogrel Arm: Incidence of All-cause Mortality and MI | 285 of 3,889 261 of 3,865 | 0.6 points -0.6 to 1.7 | 7,754 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| Cangrelor Arm vs Clopidogrel Arm: Individual Incidence of IDR | 13 of 3,889 23 of 3,865 | -0.3 points -0.6 to 0.0 | 7,754 | NCT00305162 A Clinical Trial to Demonstrate the Efficacy of Cangrelor |
| S-268019-b vs Placebo: Number of Participants With First Occurrence of SARS-CoV-2 Reverse Transcription Polymerase Chain Reaction (RT-PCR)-Positive Symptomatic COVID-19 With Onset at Least 14 Days Following Second Vaccination During the Initial Vaccination Period | 323 of 5,156 239 of 2,595 | -2.9 points -4.3 to -1.7 | 7,751 | NCT05212948 A Study of S-268019 for the Prevention of COVID-19 |
| S-268019-b vs Placebo: Number of Participants With First Occurrence of Asymptomatic SARS-CoV-2 Infection in the Initial Vaccination Period | 2,543 of 5,156 1,345 of 2,595 | -2.5 points -4.9 to -0.2 | 7,751 | NCT05212948 A Study of S-268019 for the Prevention of COVID-19 |
| BMD Result Letter and Brochure vs Control: Guideline Concordant Osteoporosis Therapy | 2,537 of 3,898 2,477 of 3,851 | 0.8 points -1.4 to 2.9 | 7,749 | NCT01507662 Patient Activation After DXA Result Notification |
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=61
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"id": "NCT05212948-fd393d94",
"title": "S-268019-b vs Placebo: Number of Participants With First Occurrence of SARS-CoV-2 RT-PCR-Positive Severe COVID-19 in the Initial Vaccination Period With Onset at Least 14 Days Following Second Vaccination",
"summary": "0 of 5181 against 1 of 2617; risk difference -0.0 points, 95% interval -0.2 to 0.0; NCT05212948, A Study of S-268019 for the Prevention of COVID-19",
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"trial_title": "A Study of S-268019 for the Prevention of COVID-19"
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{
"id": "NCT01488578-069e2f39",
"title": "Male vs Female: Risk Factors for the Proportion of Responders of Tolterodine-Gender",
"summary": "2745 of 3394 against 3791 of 4386; risk difference -5.6 points, 95% interval -7.2 to -3.9; NCT01488578, Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan)",
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"terms": [
{
"source": "ClinicalTrials.gov's posted results, through CTTI's AACT",
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"license": "none stated",
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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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Search clinical trials by condition, drug, outcome or NCT number, with the results each one posted.
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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