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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 last741 to 760 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Insulin Glargine vs Standard Care: serious adverse events | 303 of 6,231 232 of 6,273 | 1.2 points 0.5 to 1.9 | 12,504 | NCT00069784 The ORIGIN Trial (Outcome Reduction With Initial Glargine Intervention) |
| Part A (Open-label): Analysis Group 1 (AG1) + Analysis Group 3 (AG3) vs Part A (Open-label): Analysis Group 2-1 (AG2-1) + Analysis Group 4-1 (AG4-1): Part A: Number of Participants With First COVE-based COVID-19 Occurrence From 1 Day After Month 0 Dose to Month 6 Dose in FAS Cohort, Comparing Baseline SARS-CoV-2 Negative vs Positive, Regardless of HIV Statu | 34 of 2,867 45 of 9,613 | 0.7 points 0.3 to 1.2 | 12,480 | NCT05168813 Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern |
| Part A (Open-label): Analysis Group 1 (AG1) + Analysis Group 3 (AG3) vs Part A (Open-label): Analysis Group 2-1 (AG2-1) + Analysis Group 4-1 (AG4-1): Part A: Number of Participants With First CDC-based COVID-19 Occurrence From 1 Day After Month 0 Dose to Month 6 Dose in FAS Cohort, Comparing Baseline SARS-CoV-2 Negative vs Positive, Regardless of HIV Status | 86 of 2,867 179 of 9,613 | 1.1 points 0.5 to 1.9 | 12,480 | NCT05168813 Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern |
| Part A (Open-label): Analysis Group 1 (AG1) + Analysis Group 3 (AG3) vs Part A (Open-label): Analysis Group 2-1 (AG2-1) + Analysis Group 4-1 (AG4-1): Part A: Number of Participants With First COVE-based Severe COVID-19 Occurrence From 1 Day After Month 0 Dose to Month 6 Dose in FAS Cohort, Comparing Baseline SARS-CoV-2 Negative vs Positive, Regardless of HI | 7 of 2,867 6 of 9,613 | 0.2 points 0.0 to 0.4 | 12,480 | NCT05168813 Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern |
| ACP Video Program vs Usual ACP Procedures: Proportion of Target Cohort Receiving Any Burdensome Treatment | 453 of 4,171 971 of 8,308 | -0.8 points -2.0 to 0.4 | 12,479 | NCT02612688 Pragmatic Trial of Video Education in Nursing Homes |
| ACP Video Program vs Usual ACP Procedures: Proportion of Target Cohort That Has Medicare ACP Billing Codes | 356 of 4,171 685 of 8,308 | 0.3 points -0.7 to 1.3 | 12,479 | NCT02612688 Pragmatic Trial of Video Education in Nursing Homes |
| ACP Video Program vs Usual ACP Procedures: Proportion of Target Cohort With Any Hospice Enrollment | 904 of 4,171 1,878 of 8,308 | -0.9 points -2.5 to 0.6 | 12,479 | NCT02612688 Pragmatic Trial of Video Education in Nursing Homes |
| M-001 vs Saline: deaths from any cause | 26 of 6,230 29 of 6,230 | -0.0 points -0.3 to 0.2 | 12,460 | NCT03450915 A Pivotal Trial to Assess the Safety and Clinical Efficacy of the M-001 as a Standalone Universal Flu Vaccine |
| M-001 vs Saline: serious adverse events | 185 of 6,230 177 of 6,230 | 0.1 points -0.5 to 0.7 | 12,460 | NCT03450915 A Pivotal Trial to Assess the Safety and Clinical Efficacy of the M-001 as a Standalone Universal Flu Vaccine |
| Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): Number of Deaths | 238 of 6,216 264 of 6,162 | -0.5 points -1.2 to 0.2 | 12,378 | NCT00388674 Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection |
| Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): Number of Participants With HCC Malignant Neoplasm | 240 of 6,216 263 of 6,162 | -0.4 points -1.1 to 0.3 | 12,378 | NCT00388674 Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection |
| Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): Number of Participants With Liver-related HBV Disease Progression | 350 of 6,216 375 of 6,162 | -0.5 points -1.3 to 0.4 | 12,378 | NCT00388674 Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection |
| Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): Number of Participants With Non-HCC Malignant Neoplasm | 95 of 6,216 81 of 6,162 | 0.2 points -0.2 to 0.6 | 12,378 | NCT00388674 Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection |
| Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): Number of Participants With Adjudicated Overall Malignant Neoplasms | 331 of 6,216 337 of 6,162 | -0.1 points -0.9 to 0.7 | 12,378 | NCT00388674 Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection |
| Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): Number of Participants With Liver-related Death | 46 of 6,216 48 of 6,162 | -0.0 points -0.4 to 0.3 | 12,378 | NCT00388674 Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection |
| Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): serious adverse events | 56 of 6,216 50 of 6,162 | 0.1 points -0.2 to 0.4 | 12,378 | NCT00388674 Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection |
| CDS Pathway (Pre-Trial) vs CDS Pathway (Post-Trial): serious adverse events | 0 of 6,824 8 of 5,424 | -0.1 points -0.3 to -0.1 | 12,248 | NCT04263363 Applying Best Clinical Practices to Patients at High Risk of Respiratory Complications |
| Low Molecular Weight Heparin (LMWH)-Enoxaparin vs Acetylsalicylic Acid (ASA)-Aspirin: Deep Surgical Site Infection | 93 of 6,110 103 of 6,101 | -0.2 points -0.6 to 0.3 | 12,211 | NCT02984384 PREVENTion of Clot in Orthopaedic Trauma |
| Low Molecular Weight Heparin (LMWH)-Enoxaparin vs Acetylsalicylic Acid (ASA)-Aspirin: Number of Participants With All-cause Mortality | 45 of 6,110 47 of 6,101 | -0.0 points -0.3 to 0.3 | 12,211 | NCT02984384 PREVENTion of Clot in Orthopaedic Trauma |
| Low Molecular Weight Heparin (LMWH)-Enoxaparin vs Acetylsalicylic Acid (ASA)-Aspirin: Non-fatal Pulmonary Embolism | 90 of 6,110 90 of 6,101 | -0.0 points -0.4 to 0.4 | 12,211 | NCT02984384 PREVENTion of Clot in Orthopaedic Trauma |
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=38
{
"data": {
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{
"id": "NCT00069784-sae",
"title": "Insulin Glargine vs Standard Care: serious adverse events",
"summary": "303 of 6231 against 232 of 6273; risk difference 1.2 points, 95% interval 0.5 to 1.9; NCT00069784, The ORIGIN Trial (Outcome Reduction With Initial Glargine Intervention)",
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{
"id": "NCT05168813-49517fe3",
"title": "Part A (Open-label): Analysis Group 1 (AG1) + Analysis Group 3 (AG3) vs Part A (Open-label): Analysis Group 2-1 (AG2-1) + Analysis Group 4-1 (AG4-1): Part A: Number of Participants With First COVE-based COVID-19 Occurrence From 1 Day After Month 0 Dose to Month 6 Dose in FAS Cohort, Comparing Baseline SARS-CoV-2 Negative vs Positive, Regardless of HIV Statu",
"summary": "34 of 2867 against 45 of 9613; risk difference 0.7 points, 95% interval 0.3 to 1.2; NCT05168813, Efficacy Study of COVID-19 mRNA Vaccine in Regions With SARS-CoV-2 Variants of Concern",
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"terms": [
{
"source": "ClinicalTrials.gov's posted results, through CTTI's AACT",
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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
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