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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 last1,601 to 1,620 of 85,013

Show the results as
ComparisonWith the outcomeRisk difference, 95% intervalParticipantsTrial
Intervention - Fall Prevention Standard of Care vs Control: serious adverse events1,139 of 2,802

1,108 of 2,649

-1.2 points

-3.8 to 1.4

5,451NCT02475850

Strategies to Reduce Injuries and Develop Confidence in Elders

Vaccine vs Placebo: deaths from any cause8 of 2,704

10 of 2,700

-0.1 points

-0.4 to 0.3

5,404NCT02968849

Pivotal Phase 2b/3 ALVAC/Bivalent gp120/MF59 HIV Vaccine Prevention Safety and Efficacy Study in South Africa

Vaccine vs Placebo: serious adverse events103 of 2,704

95 of 2,700

0.3 points

-0.7 to 1.3

5,404NCT02968849

Pivotal Phase 2b/3 ALVAC/Bivalent gp120/MF59 HIV Vaccine Prevention Safety and Efficacy Study in South Africa

At Risk Body Weight vs Normal Body Weight: Diagnosis of Infectious Disease900 of 2,361

1,067 of 3,031

2.9 points

0.3 to 5.5

5,392NCT00267631

Impact of Body Weight on the Immediate Health of the Pediatric Population

Dabigatran Etexilate 110 or 150 Milligram (mg) vs Acetylsalicylic Acid, Aspirin (ASA) 100 mg: deaths from any cause56 of 2,695

58 of 2,695

-0.1 points

-0.9 to 0.7

5,390NCT02239120

Dabigatran Etexilate for Secondary Stroke Prevention in Patients With Embolic Stroke of Undetermined Source (RE-SPECT ESUS)

Descovy (DVY) vs Truvada (TVD): deaths from any cause3 of 2,694

3 of 2,693

-0.0 points

-0.2 to 0.2

5,387NCT02842086

Study to Evaluate the Safety and Efficacy of Emtricitabine and Tenofovir Alafenamide (F/TAF) Fixed-Dose Combination Once Daily for Pre-Exposure Prophylaxis in Men and Transgender Women Who Have Sex With Men and Are At Risk of HIV-1 Infection

Descovy (DVY) vs Truvada (TVD): serious adverse events202 of 2,694

186 of 2,693

0.6 points

-0.8 to 2.0

5,387NCT02842086

Study to Evaluate the Safety and Efficacy of Emtricitabine and Tenofovir Alafenamide (F/TAF) Fixed-Dose Combination Once Daily for Pre-Exposure Prophylaxis in Men and Transgender Women Who Have Sex With Men and Are At Risk of HIV-1 Infection

0.9% Sodium Chloride (Saline) vs Balanced Crystalloid: Major Adverse Kidney Event Within 30 Days659 of 2,646

615 of 2,735

2.4 points

0.1 to 4.7

5,381NCT02444988

Isotonic Solutions and Major Adverse Renal Events Trial in the Medical Intensive Care Unit

0.9% Sodium Chloride (Saline) vs Balanced Crystalloid: deaths from any cause467 of 2,646

418 of 2,735

2.4 points

0.4 to 4.4

5,381NCT02444988

Isotonic Solutions and Major Adverse Renal Events Trial in the Medical Intensive Care Unit

0.9% Sodium Chloride (Saline) vs Balanced Crystalloid: 30-day In-hospital Mortality467 of 2,646

418 of 2,735

2.4 points

0.4 to 4.4

5,381NCT02444988

Isotonic Solutions and Major Adverse Renal Events Trial in the Medical Intensive Care Unit

Alogliptin vs Placebo: serious adverse events907 of 2,701

952 of 2,679

-2.0 points

-4.5 to 0.6

5,380NCT00968708

Cardiovascular Outcomes Study of Alogliptin in Patients With Type 2 Diabetes and Acute Coronary Syndrome

Apixaban vs Enoxaparin/Warfarin: serious adverse events417 of 2,676

410 of 2,689

0.3 points

-1.6 to 2.3

5,365NCT00643201

Efficacy and Safety Study of Apixaban for the Treatment of Deep Vein Thrombosis or Pulmonary Embolism

Dabigatran Etexilate 110 or 150 Milligram (mg) vs Acetylsalicylic Acid, Aspirin (ASA) 100 mg: serious adverse events724 of 2,676

740 of 2,674

-0.6 points

-3.0 to 1.8

5,350NCT02239120

Dabigatran Etexilate for Secondary Stroke Prevention in Patients With Embolic Stroke of Undetermined Source (RE-SPECT ESUS)

Individualized Opioid Prescription vs Fixed Opioid Prescription: Number of Participants Who Filled One or More Opioid Prescriptions Beyond the Amount Prescribed at Discharge200 of 2,654

166 of 2,696

1.4 points

0.0 to 2.7

5,350NCT04296396

Opioid Prescription After Cesarean Trial

Telmisartan (TRANSCEND) vs Placebo (TRANSCEND): TRANSCEND. New Macroalbuminuria66 of 2,658

101 of 2,676

-1.3 points

-2.2 to -0.4

5,334NCT00153101

Effectiveness and Safety of Ramipril Alone Compared With Telmisartan Alone and in Combination With Ramipril in Patients at High Risk for Cardiovascular Events. Patients Intolerant to Ramipril Were Entered in TRANSCEND, Telmisartan Compared to Placebo.

Apixaban, 2.5 mg BID + Placebo vs Enoxaparin, 40 mg QD + Placebo: serious adverse events184 of 2,673

172 of 2,659

0.4 points

-0.9 to 1.8

5,332NCT00423319

Study of an Investigational Drug for the Prevention of Thrombosis-related Events Following Hip Replacement Surgery (ADVANCE-3)

RSV MAT Group - Mother vs Placebo Group - Mother: Number of Maternal Participants With at Least One AE Leading to Study Withdrawal From Day 1 to Day 181 Post-delivery6 of 3,557

3 of 1,771

-0.0 points

-0.3 to 0.2

5,328NCT04605159

A Phase III, Double-blind Study to Assess Safety and Efficacy of an RSV Maternal Unadjuvanted Vaccine, in Pregnant Women and Infants Born to Vaccinated Mothers

RSV MAT Group - Mother vs Placebo Group - Mother: Number of Maternal Participants With RSV-associated Medically Attended RTIs (RSV-MA-RTIs) From Study Intervention Administration (Day 1) to Day 181 Post-delivery3 of 3,557

6 of 1,771

-0.3 points

-0.7 to -0.0

5,328NCT04605159

A Phase III, Double-blind Study to Assess Safety and Efficacy of an RSV Maternal Unadjuvanted Vaccine, in Pregnant Women and Infants Born to Vaccinated Mothers

RSV MAT Group - Mother vs Placebo Group - Mother: Number of Maternal Participants With Any Unsolicited AEs From Day 1 to Day 30 Included629 of 3,557

297 of 1,771

0.9 points

-1.3 to 3.0

5,328NCT04605159

A Phase III, Double-blind Study to Assess Safety and Efficacy of an RSV Maternal Unadjuvanted Vaccine, in Pregnant Women and Infants Born to Vaccinated Mothers

RSV MAT Group - Mother vs Placebo Group - Mother: Number of Maternal Participants With at Least One MAE From Day 1 to Day 42 Post-delivery1,717 of 3,557

785 of 1,771

3.9 points

1.1 to 6.8

5,328NCT04605159

A Phase III, Double-blind Study to Assess Safety and Efficacy of an RSV Maternal Unadjuvanted Vaccine, in Pregnant Women and Infants Born to Vaccinated Mothers

Request

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=81

{
  "data": {
    "total": 85013,
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      {
        "id": "NCT02475850-sae",
        "title": "Intervention - Fall Prevention Standard of Care vs Control: serious adverse events",
        "summary": "1139 of 2802 against 1108 of 2649; risk difference -1.2 points, 95% interval -3.8 to 1.4; NCT02475850, Strategies to Reduce Injuries and Develop Confidence in Elders",
        "record": "/library/comparisons/NCT02475850-sae",
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        "kind": "serious-adverse-events",
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          "lower": -0.03790028765493776,
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        },
        "group_1": "1,139 of 2,802",
        "group_2": "1,108 of 2,649",
        "difference": "-1.2 points",
        "interval": "-3.8 to 1.4",
        "trial_title": "Strategies to Reduce Injuries and Develop Confidence in Elders"
      },
      {
        "id": "NCT02968849-deaths",
        "title": "Vaccine vs Placebo: deaths from any cause",
        "summary": "8 of 2704 against 10 of 2700; risk difference -0.1 points, 95% interval -0.4 to 0.3; NCT02968849, Pivotal Phase 2b/3 ALVAC/Bivalent gp120/MF59 HIV Vaccine Prevention Safety and Efficacy Study in South Africa",
        "record": "/library/comparisons/NCT02968849-deaths",
        "nct_id": "NCT02968849",
        "kind": "deaths",
        "participants": 5404,
        "risk_difference": {
          "value": -0.0007451238220468992,
          "lower": -0.004171944832423495,
          "upper": 0.0025848820706288636
        },
        "group_1": "8 of 2,704",
        "group_2": "10 of 2,700",
        "difference": "-0.1 points",
        "interval": "-0.4 to 0.3",
        "trial_title": "Pivotal Phase 2b/3 ALVAC/Bivalent gp120/MF59 HIV Vaccine Prevention Safety and Efficacy Study in South Africa"
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      "outcome": 33568,
      "serious-adverse-events": 31897,
      "deaths": 19548
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      "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.",
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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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