Genes
NCBI Gene
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 last4,761 to 4,780 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Cohort 1: Participants Aged 9 to 17 Years vs Cohort 2: Participants Aged 18 to 49 Years: Number of Participants With Medically Attended Adverse Events (MAAEs) | 27 of 641 35 of 658 | -1.1 points -3.5 to 1.3 | 1,299 | NCT05513053 Study With Quadrivalent Recombinant Influenza Vaccine (RIV4) in Participants 9 Through 49 Years of Age. |
| Cohort 1: Participants Aged 9 to 17 Years vs Cohort 2: Participants Aged 18 to 49 Years: serious adverse events | 3 of 641 7 of 658 | -0.6 points -1.8 to 0.5 | 1,299 | NCT05513053 Study With Quadrivalent Recombinant Influenza Vaccine (RIV4) in Participants 9 Through 49 Years of Age. |
| Proactive Group vs Reactive Group: serious adverse events | 16 of 649 6 of 649 | 1.5 points 0.1 to 3.1 | 1,298 | NCT00632411 Evaluating a Telephone-Based Smoking Cessation Program Among People in the Military (The AFIII Study) |
| Aggrenox Capsule vs Acetylsalicylic Acid (ASA) 81 mg Tablet: serious adverse events | 178 of 655 167 of 639 | 1.0 points -3.8 to 5.8 | 1,294 | NCT00311402 JASAP: Japanese Aggrenox Stroke Prevention vs. Aspirin Programme |
| Symbicort Turbuhaler (Experimental) vs Oxis Turbuhaler (Active Comparator): serious adverse events | 43 of 636 45 of 657 | -0.1 points -2.9 to 2.7 | 1,293 | NCT01069289 Efficacy and Safety Study of Symbicort® Turbuhaler® Versus Oxis® Turbuhaler® in Chronic Obstructive Pulmonary Disease (COPD) Patients |
| GBC+PIPT vs Guideline Based Care: Number of Patients Who Reported Transition From Acute to Chronic Low Back Pain (cLBP) | 312 of 658 318 of 635 | -2.7 points -8.1 to 2.8 | 1,293 | NCT02647658 Targeted Interventions to Prevent Chronic Low Back Pain in High Risk Patients |
| 5 mg Risedronate vs 150 mg Risedronate: Number of Participants With New Vertebral Fracture at Month 12, ITT Population | 8 of 642 8 of 650 | 0.0 points -1.3 to 1.4 | 1,292 | NCT00247273 A Study of Monthly Risedronate for Osteoporosis |
| 5 mg Risedronate vs 150 mg Risedronate: Number of Participants With New Vertebral Fracture at Month 24, ITT Population | 14 of 642 14 of 650 | 0.0 points -1.6 to 1.7 | 1,292 | NCT00247273 A Study of Monthly Risedronate for Osteoporosis |
| 5 mg Risedronate vs 150 mg Risedronate: serious adverse events | 51 of 642 77 of 650 | -3.9 points -7.2 to -0.6 | 1,292 | NCT00247273 A Study of Monthly Risedronate for Osteoporosis |
| Icodec vs IcoSema: deaths from any cause | 3 of 645 2 of 646 | 0.2 points -0.7 to 1.1 | 1,291 | NCT05352815 A Research Study to See How Well the New Weekly Medicine IcoSema, Which is a Combination of Insulin Icodec and Semaglutide, Controls Blood Sugar Level in People With Type 2 Diabetes Compared to Weekly Insulin Icodec |
| Arm B - Fluvoxamine 50 vs Arm B - Placebo: serious adverse events | 3 of 676 6 of 615 | -0.5 points -1.7 to 0.5 | 1,291 | NCT05890586 ACTIV-6: COVID-19 Study of Repurposed Medications - Arm B (Fluvoxamine) |
| Best Practice Clinic-Based Care vs Telehealth Care: Number of Participants Who Report High Level of Satisfaction With Hypertension Care at Six Months. | 205 of 678 241 of 610 | -9.3 points -14.4 to -4.1 | 1,288 | NCT02996565 Pragmatic Trial Comparing Telehealth Care and Optimized Clinic-Based Care for Uncontrolled High Blood Pressure |
| Nirmatrelvir 300 mg + Ritonavir 100 mg vs Placebo: deaths from any cause | 0 of 654 1 of 634 | -0.2 points -0.9 to 0.4 | 1,288 | NCT05011513 Evaluation of Protease Inhibition for COVID-19 in Standard-Risk Patients (EPIC-SR). |
| Nirmatrelvir 300 mg + Ritonavir 100 mg vs Placebo: serious adverse events | 8 of 654 13 of 634 | -0.8 points -2.4 to 0.6 | 1,288 | NCT05011513 Evaluation of Protease Inhibition for COVID-19 in Standard-Risk Patients (EPIC-SR). |
| Icodec vs IcoSema: serious adverse events | 69 of 644 59 of 644 | 1.6 points -1.7 to 4.8 | 1,288 | NCT05352815 A Research Study to See How Well the New Weekly Medicine IcoSema, Which is a Combination of Insulin Icodec and Semaglutide, Controls Blood Sugar Level in People With Type 2 Diabetes Compared to Weekly Insulin Icodec |
| Placebo + Letrozole 2.5 mg vs Lapatinib 1500 mg + Letrozole 2.5 mg: Number of Participants With PFS in the Intent-To-Treat (ITT) Population as Assessed by the Investigator | 476 of 644 413 of 642 | 9.6 points 4.5 to 14.6 | 1,286 | NCT00073528 Study Comparing Lapatinib (GW572016) And Letrozole Versus Letrozole In Subjects With Advanced Or Metastatic Breast Cancer |
| Placebo + Letrozole 2.5 mg vs Lapatinib 1500 mg + Letrozole 2.5 mg: Number of Participants With Evidence of Brain Metastases From the ITT Population | 4 of 644 6 of 642 | -0.3 points -1.5 to 0.8 | 1,286 | NCT00073528 Study Comparing Lapatinib (GW572016) And Letrozole Versus Letrozole In Subjects With Advanced Or Metastatic Breast Cancer |
| Gain-Framed Counseling vs Standard Care Counseling: 7 Day Abstinence | 148 of 524 202 of 762 | 1.7 points -3.2 to 6.7 | 1,286 | NCT00589277 Message Framing for Telephone Quitline Callers |
| Atezolizumab With Paclitaxel, Carboplatin and Bevacizumab vs Placebo With Paclitaxel, Carboplatin and Bevacizumab: serious adverse events | 304 of 642 215 of 644 | 14.0 points 8.6 to 19.2 | 1,286 | NCT03038100 A Study of Atezolizumab Versus Placebo in Combination With Paclitaxel, Carboplatin, and Bevacizumab in Participants With Newly-Diagnosed Stage III or Stage IV Ovarian, Fallopian Tube, or Primary Peritoneal Cancer |
| Treatment vs Placebo: Rate of All-Cause Study Medicine Discontinuation or Withdrawal | 97 of 645 63 of 641 | 5.2 points 1.6 to 8.8 | 1,286 | NCT04308668 Post-exposure Prophylaxis / Preemptive Therapy for SARS-Coronavirus-2 |
Code
curl "https://conductscience.org/api/comparisons/v1?page=239"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=239
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT05513053-8d124c6a",
"title": "Cohort 1: Participants Aged 9 to 17 Years vs Cohort 2: Participants Aged 18 to 49 Years: Number of Participants With Medically Attended Adverse Events (MAAEs)",
"summary": "27 of 641 against 35 of 658; risk difference -1.1 points, 95% interval -3.5 to 1.3; NCT05513053, Study With Quadrivalent Recombinant Influenza Vaccine (RIV4) in Participants 9 Through 49 Years of Age.",
"record": "/library/comparisons/NCT05513053-8d124c6a",
"nct_id": "NCT05513053",
"kind": "outcome",
"participants": 1299,
"risk_difference": {
"value": -0.01106980449430743,
"lower": -0.03483570959191211,
"upper": 0.012534972395294552
},
"group_1": "27 of 641",
"group_2": "35 of 658",
"difference": "-1.1 points",
"interval": "-3.5 to 1.3",
"trial_title": "Study With Quadrivalent Recombinant Influenza Vaccine (RIV4) in Participants 9 Through 49 Years of Age."
},
{
"id": "NCT05513053-sae",
"title": "Cohort 1: Participants Aged 9 to 17 Years vs Cohort 2: Participants Aged 18 to 49 Years: serious adverse events",
"summary": "3 of 641 against 7 of 658; risk difference -0.6 points, 95% interval -1.8 to 0.5; NCT05513053, Study With Quadrivalent Recombinant Influenza Vaccine (RIV4) in Participants 9 Through 49 Years of Age.",
"record": "/library/comparisons/NCT05513053-sae",
"nct_id": "NCT05513053",
"kind": "serious-adverse-events",
"participants": 1299,
"risk_difference": {
"value": -0.005958110664852126,
"lower": -0.017533840869292397,
"upper": 0.004567126080172845
},
"group_1": "3 of 641",
"group_2": "7 of 658",
"difference": "-0.6 points",
"interval": "-1.8 to 0.5",
"trial_title": "Study With Quadrivalent Recombinant Influenza Vaccine (RIV4) in Participants 9 Through 49 Years of Age."
}
],
"no_events": 33758,
"columns": [
{
"key": "title",
"label": "Comparison"
},
{
"key": "group_1",
"label": "With the outcome",
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},
{
"key": "difference",
"label": "Risk difference, 95% interval",
"under": "interval"
},
{
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},
{
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],
"order": "Most participants first",
"kinds": {
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"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=240",
"request_id": "9LPcez_ty0vvZRff"
}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.
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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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