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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 last1,601 to 1,620 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Intervention - Fall Prevention Standard of Care vs Control: serious adverse events | 1,139 of 2,802 1,108 of 2,649 | -1.2 points -3.8 to 1.4 | 5,451 | NCT02475850 Strategies to Reduce Injuries and Develop Confidence in Elders |
| Vaccine vs Placebo: deaths from any cause | 8 of 2,704 10 of 2,700 | -0.1 points -0.4 to 0.3 | 5,404 | NCT02968849 Pivotal Phase 2b/3 ALVAC/Bivalent gp120/MF59 HIV Vaccine Prevention Safety and Efficacy Study in South Africa |
| Vaccine vs Placebo: serious adverse events | 103 of 2,704 95 of 2,700 | 0.3 points -0.7 to 1.3 | 5,404 | NCT02968849 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 Disease | 900 of 2,361 1,067 of 3,031 | 2.9 points 0.3 to 5.5 | 5,392 | NCT00267631 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 cause | 56 of 2,695 58 of 2,695 | -0.1 points -0.9 to 0.7 | 5,390 | NCT02239120 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 cause | 3 of 2,694 3 of 2,693 | -0.0 points -0.2 to 0.2 | 5,387 | NCT02842086 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 events | 202 of 2,694 186 of 2,693 | 0.6 points -0.8 to 2.0 | 5,387 | NCT02842086 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 Days | 659 of 2,646 615 of 2,735 | 2.4 points 0.1 to 4.7 | 5,381 | NCT02444988 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 cause | 467 of 2,646 418 of 2,735 | 2.4 points 0.4 to 4.4 | 5,381 | NCT02444988 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 Mortality | 467 of 2,646 418 of 2,735 | 2.4 points 0.4 to 4.4 | 5,381 | NCT02444988 Isotonic Solutions and Major Adverse Renal Events Trial in the Medical Intensive Care Unit |
| Alogliptin vs Placebo: serious adverse events | 907 of 2,701 952 of 2,679 | -2.0 points -4.5 to 0.6 | 5,380 | NCT00968708 Cardiovascular Outcomes Study of Alogliptin in Patients With Type 2 Diabetes and Acute Coronary Syndrome |
| Apixaban vs Enoxaparin/Warfarin: serious adverse events | 417 of 2,676 410 of 2,689 | 0.3 points -1.6 to 2.3 | 5,365 | NCT00643201 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 events | 724 of 2,676 740 of 2,674 | -0.6 points -3.0 to 1.8 | 5,350 | NCT02239120 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 Discharge | 200 of 2,654 166 of 2,696 | 1.4 points 0.0 to 2.7 | 5,350 | NCT04296396 Opioid Prescription After Cesarean Trial |
| Telmisartan (TRANSCEND) vs Placebo (TRANSCEND): TRANSCEND. New Macroalbuminuria | 66 of 2,658 101 of 2,676 | -1.3 points -2.2 to -0.4 | 5,334 | NCT00153101 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 events | 184 of 2,673 172 of 2,659 | 0.4 points -0.9 to 1.8 | 5,332 | NCT00423319 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-delivery | 6 of 3,557 3 of 1,771 | -0.0 points -0.3 to 0.2 | 5,328 | NCT04605159 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-delivery | 3 of 3,557 6 of 1,771 | -0.3 points -0.7 to -0.0 | 5,328 | NCT04605159 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 Included | 629 of 3,557 297 of 1,771 | 0.9 points -1.3 to 3.0 | 5,328 | NCT04605159 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-delivery | 1,717 of 3,557 785 of 1,771 | 3.9 points 1.1 to 6.8 | 5,328 | NCT04605159 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 |
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=81
{
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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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},
{
"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",
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"terms": [
{
"source": "ClinicalTrials.gov's posted results, through CTTI's AACT",
"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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}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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