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One gene with its proteins, patents, drugs, trials, grants and papers.
85,013 comparisons from ClinicalTrials.gov.
Most participants first33,758 with no events in either group come last3,301 to 3,320 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Motavizumab vs Placebo: Number of Participants With RSV Outpatient Medically Attended Lower Respiratory Illness (MA LRI) | 41 of 1,417 71 of 710 | -7.1 points -9.6 to -4.9 | 2,127 | NCT00121108 MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States |
| Motavizumab vs Placebo: Number of Participants With Medically Attended-Otitis Media (MA-OM) Events | 532 of 1,417 275 of 710 | -1.2 points -5.6 to 3.2 | 2,127 | NCT00121108 MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States |
| Motavizumab vs Placebo: Number of Participants With Respiratory Syncytial Virus (RSV) Hospitalization | 21 of 1,417 80 of 710 | -9.8 points -12.4 to -7.5 | 2,127 | NCT00121108 MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States |
| NOMAC-E2 vs DRSP-EE: serious adverse events | 38 of 1,591 13 of 535 | -0.0 points -1.8 to 1.3 | 2,126 | NCT00511199 Efficacy and Safety of the Combined Oral Contraceptive (COC) NOMAC-E2 Compared to a COC Containing DRSP/EE (292001)(COMPLETED)(P05724) |
| MOTAVIZUMAB vs PLACEBO: deaths from any cause | 8 of 1,414 5 of 708 | -0.1 points -1.1 to 0.5 | 2,122 | NCT00121108 MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States |
| MOTAVIZUMAB vs PLACEBO: serious adverse events | 212 of 1,414 148 of 708 | -5.9 points -9.5 to -2.5 | 2,122 | NCT00121108 MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States |
| Old Lina vs New Lina: Frequency of Patients With Adjudication of Cardiac and Cerebrovascular Events | 82 of 1,532 37 of 589 | -0.9 points -3.4 to 1.2 | 2,121 | NCT00736099 Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM |
| Old Lina vs New Lina: Frequency of Patients With Investigator-defined Hypoglycaemic Adverse Events | 209 of 1,532 86 of 589 | -1.0 points -4.4 to 2.2 | 2,121 | NCT00736099 Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM |
| Old Lina vs New Lina: serious adverse events | 158 of 1,532 52 of 589 | 1.5 points -1.5 to 4.1 | 2,121 | NCT00736099 Safety and Efficacy of Linagliptin (BI 1356) as Monotherapy or in Combination in Type 2 DM |
| MRSA Decolonization vs Education Arm: Rehospitalization Due to MRSA Infection | 57 of 1,058 83 of 1,063 | -2.4 points -4.6 to -0.3 | 2,121 | NCT01209234 Project CLEAR - Changing Lives by Eradicating Antibiotic Resistance |
| Nirsevimab vs No Intervention: Number of Participants With Hospitalization for All-Cause Lower Respiratory Tract Infection From Days 366 to 731 Post-dosing/Randomization (for United Kingdom Reconsented Participants) | 18 of 1,096 10 of 1,025 | 0.7 points -0.3 to 1.7 | 2,121 | NCT05437510 Study of a Single Intramuscular Dose of Nirsevimab in the Prevention of Hospitalizations Due to Respiratory Syncytial Virus (RSV) Infection in Healthy Term and Preterm Infants During the First Year of Life |
| VF Induction vs No- VF Induction: Sudden Cardiac Death at Follow up or Resusciation After Ineffective Documented Appropriate ICD Shocks at Follow up | 10 of 836 12 of 1,284 | 0.3 points -0.6 to 1.3 | 2,120 | NCT00661037 SAFEty of Two Strategies of ICD Management at Implantation |
| VF Induction vs no VF Induction: Severe Intra-operative Complications | 8 of 836 4 of 1,284 | 0.6 points -0.0 to 1.6 | 2,120 | NCT00661037 SAFEty of Two Strategies of ICD Management at Implantation |
| VF Induction vs no VF Induction: deaths from any cause | 108 of 836 188 of 1,284 | -1.7 points -4.7 to 1.3 | 2,120 | NCT00661037 SAFEty of Two Strategies of ICD Management at Implantation |
| VF Induction vs no VF Induction: Number of Participants With Severe Intra-operative Complications at ICD Implant and/or Events at Follow up | 18 of 836 16 of 1,284 | 0.9 points -0.2 to 2.2 | 2,120 | NCT00661037 SAFEty of Two Strategies of ICD Management at Implantation |
| VF Induction vs no VF Induction: serious adverse events | 209 of 836 177 of 1,284 | 11.2 points 7.8 to 14.7 | 2,120 | NCT00661037 SAFEty of Two Strategies of ICD Management at Implantation |
| DVS SR 100 mg vs Placebo: Number of Participants With Hepatic Events | 2 of 1,066 2 of 1,052 | -0.0 points -0.5 to 0.5 | 2,118 | NCT00683800 Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women |
| DVS SR 100 mg vs Placebo: Number of Participants With Adjudicated Cerebrovascular Events - Probable TIA | 1 of 1,066 0 of 1,052 | 0.1 points -0.3 to 0.5 | 2,118 | NCT00683800 Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women |
| DVS SR 100 mg vs Placebo: Number of Participants With Ischemic Heart Disease | 4 of 1,066 2 of 1,052 | 0.2 points -0.4 to 0.8 | 2,118 | NCT00683800 Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women |
| DVS SR 100 mg vs Placebo: serious adverse events | 43 of 1,066 36 of 1,052 | 0.6 points -1.0 to 2.3 | 2,118 | NCT00683800 Study Evaluating The Safety And Efficacy Of Desvenlafaxine Succinate For Vasomotor Symptoms In Menopausal Women |
Code
curl "https://conductscience.org/api/comparisons/v1?page=166"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=166
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00121108-1a43adaf",
"title": "Motavizumab vs Placebo: Number of Participants With RSV Outpatient Medically Attended Lower Respiratory Illness (MA LRI)",
"summary": "41 of 1417 against 71 of 710; risk difference -7.1 points, 95% interval -9.6 to -4.9; NCT00121108, MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States",
"record": "/library/comparisons/NCT00121108-1a43adaf",
"nct_id": "NCT00121108",
"kind": "outcome",
"participants": 2127,
"risk_difference": {
"value": -0.07106563161609034,
"lower": -0.0964735215881775,
"upper": -0.04870402940926678
},
"group_1": "41 of 1,417",
"group_2": "71 of 710",
"difference": "-7.1 points",
"interval": "-9.6 to -4.9",
"trial_title": "MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States"
},
{
"id": "NCT00121108-76411a78",
"title": "Motavizumab vs Placebo: Number of Participants With Medically Attended-Otitis Media (MA-OM) Events",
"summary": "532 of 1417 against 275 of 710; risk difference -1.2 points, 95% interval -5.6 to 3.2; NCT00121108, MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States",
"record": "/library/comparisons/NCT00121108-76411a78",
"nct_id": "NCT00121108",
"kind": "outcome",
"participants": 2127,
"risk_difference": {
"value": -0.011882870973192683,
"lower": -0.05590941448863594,
"upper": 0.03154028816849494
},
"group_1": "532 of 1,417",
"group_2": "275 of 710",
"difference": "-1.2 points",
"interval": "-5.6 to 3.2",
"trial_title": "MEDI-524 (Motavizumab) for the Prevention of Respiratory Sycytial Virus (RSV) Disease Among Native American Indian Infants in the Southwestern United States"
}
],
"no_events": 33758,
"columns": [
{
"key": "title",
"label": "Comparison"
},
{
"key": "group_1",
"label": "With the outcome",
"under": "group_2"
},
{
"key": "difference",
"label": "Risk difference, 95% interval",
"under": "interval"
},
{
"key": "participants",
"label": "Participants"
},
{
"key": "nct_id",
"label": "Trial",
"under": "trial_title"
}
],
"order": "Most participants first",
"kinds": {
"all": 85013,
"outcome": 33568,
"serious-adverse-events": 31897,
"deaths": 19548
}
},
"release": "trial-comparisons-2026-03-23-0.1.0",
"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.",
"short": "Freely available. Acknowledgement requested"
},
{
"source": "ClinicalTrials.gov",
"license": "none stated",
"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.",
"short": "No license stated"
}
],
"next": "/api/comparisons/v1?page=167",
"request_id": "WxOlqYCCTRZ8c74j"
}Ask about these results. The first 10 go in the prompt.
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.
ClinicalTrials.gov
Search clinical trials by condition, drug, outcome or NCT number, with the results each one posted.
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Opens sequences.conductscience.org
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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