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85,013 comparisons from ClinicalTrials.gov. Counted 2026-11-10.

85,013 comparisons

Most participants first33,758 with no events in either group come last741 to 760 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
Insulin Glargine vs Standard Care: serious adverse events303 of 6,231

232 of 6,273

1.2 points

0.5 to 1.9

12,504NCT00069784

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 Statu34 of 2,867

45 of 9,613

0.7 points

0.3 to 1.2

12,480NCT05168813

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 Status86 of 2,867

179 of 9,613

1.1 points

0.5 to 1.9

12,480NCT05168813

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 HI7 of 2,867

6 of 9,613

0.2 points

0.0 to 0.4

12,480NCT05168813

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 Treatment453 of 4,171

971 of 8,308

-0.8 points

-2.0 to 0.4

12,479NCT02612688

Pragmatic Trial of Video Education in Nursing Homes

ACP Video Program vs Usual ACP Procedures: Proportion of Target Cohort That Has Medicare ACP Billing Codes356 of 4,171

685 of 8,308

0.3 points

-0.7 to 1.3

12,479NCT02612688

Pragmatic Trial of Video Education in Nursing Homes

ACP Video Program vs Usual ACP Procedures: Proportion of Target Cohort With Any Hospice Enrollment904 of 4,171

1,878 of 8,308

-0.9 points

-2.5 to 0.6

12,479NCT02612688

Pragmatic Trial of Video Education in Nursing Homes

M-001 vs Saline: deaths from any cause26 of 6,230

29 of 6,230

-0.0 points

-0.3 to 0.2

12,460NCT03450915

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 events185 of 6,230

177 of 6,230

0.1 points

-0.5 to 0.7

12,460NCT03450915

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 Deaths238 of 6,216

264 of 6,162

-0.5 points

-1.2 to 0.2

12,378NCT00388674

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 Neoplasm240 of 6,216

263 of 6,162

-0.4 points

-1.1 to 0.3

12,378NCT00388674

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 Progression350 of 6,216

375 of 6,162

-0.5 points

-1.3 to 0.4

12,378NCT00388674

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 Neoplasm95 of 6,216

81 of 6,162

0.2 points

-0.2 to 0.6

12,378NCT00388674

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 Neoplasms331 of 6,216

337 of 6,162

-0.1 points

-0.9 to 0.7

12,378NCT00388674

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 Death46 of 6,216

48 of 6,162

-0.0 points

-0.4 to 0.3

12,378NCT00388674

Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection

Entecavir (ETV) vs Other Anti-HBV Medication (Non-ETV): serious adverse events56 of 6,216

50 of 6,162

0.1 points

-0.2 to 0.4

12,378NCT00388674

Study of Entecavir in Patients With Chronic Hepatitis B Virus (HBV) Infection

CDS Pathway (Pre-Trial) vs CDS Pathway (Post-Trial): serious adverse events0 of 6,824

8 of 5,424

-0.1 points

-0.3 to -0.1

12,248NCT04263363

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 Infection93 of 6,110

103 of 6,101

-0.2 points

-0.6 to 0.3

12,211NCT02984384

PREVENTion of Clot in Orthopaedic Trauma

Low Molecular Weight Heparin (LMWH)-Enoxaparin vs Acetylsalicylic Acid (ASA)-Aspirin: Number of Participants With All-cause Mortality45 of 6,110

47 of 6,101

-0.0 points

-0.3 to 0.3

12,211NCT02984384

PREVENTion of Clot in Orthopaedic Trauma

Low Molecular Weight Heparin (LMWH)-Enoxaparin vs Acetylsalicylic Acid (ASA)-Aspirin: Non-fatal Pulmonary Embolism90 of 6,110

90 of 6,101

-0.0 points

-0.4 to 0.4

12,211NCT02984384

PREVENTion of Clot in Orthopaedic Trauma

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GET /api/comparisons/v1

Words from a trial's title, conditions or interventions, its outcome or its groups, or an NCT number.

An outcome counted in participants, the serious adverse events, or the deaths from any cause.

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Response

The first 2 of this page's 20 results. GET /api/comparisons/v1?page=38

{
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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",
        "record": "/library/comparisons/NCT05168813-49517fe3",
        "nct_id": "NCT05168813",
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        "group_1": "34 of 2,867",
        "group_2": "45 of 9,613",
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        "interval": "0.3 to 1.2",
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trial-comparisons-2026-03-23-0.1.0Next page

Sources 2

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNone stated
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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
  • ClinicalTrials.govnone stated

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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