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85,013 comparisons from ClinicalTrials.gov.
Most participants first33,758 with no events in either group come last1,961 to 1,980 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Celecoxib vs Oral Diclofenac Plus Omeprazole: Number of Subjects With SUs | 5 of 2,238 11 of 2,246 | -0.3 points -0.7 to 0.1 | 4,484 | NCT00141102 Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis |
| Celecoxib vs Oral Diclofenac Plus Omeprazole: Number of Subjects With CSULGIES or Symptomatic Ulcers (SUs) | 25 of 2,238 92 of 2,246 | -3.0 points -3.9 to -2.1 | 4,484 | NCT00141102 Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis |
| Celecoxib vs Oral Diclofenac Plus Omeprazole: Number of Subjects Withdrawn Due to GI Adverse Events (AEs) | 114 of 2,238 167 of 2,246 | -2.3 points -3.8 to -0.9 | 4,484 | NCT00141102 Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis |
| Targeted Indoor Residual Spraying (TIRS) vs Routine Aedes-borne Virus (ABV) Prevention and Control: deaths from any cause | 1 of 2,239 2 of 2,222 | -0.0 points -0.3 to 0.2 | 4,461 | NCT04343521 Quantifying the Epidemiological Impact of Targeted Indoor Residual Spraying on Aedes-borne Diseases |
| Targeted Indoor Residual Spraying (TIRS) vs Routine Aedes-borne Virus (ABV) Prevention and Control: serious adverse events | 0 of 2,239 2 of 2,222 | -0.1 points -0.3 to 0.1 | 4,461 | NCT04343521 Quantifying the Epidemiological Impact of Targeted Indoor Residual Spraying on Aedes-borne Diseases |
| Celecoxib vs Oral Diclofenac Plus Omeprazole: serious adverse events | 61 of 2,223 61 of 2,237 | 0.0 points -1.0 to 1.0 | 4,460 | NCT00141102 Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis |
| Denosumab vs Placebo: deaths from any cause | 215 of 2,241 215 of 2,218 | -0.1 points -1.8 to 1.6 | 4,459 | NCT01077154 Study of Denosumab as Adjuvant Treatment for Women With High Risk Early Breast Cancer Receiving Neoadjuvant or Adjuvant Therapy (D-CARE) |
| Denosumab vs Placebo: serious adverse events | 702 of 2,241 675 of 2,218 | 0.9 points -1.8 to 3.6 | 4,459 | NCT01077154 Study of Denosumab as Adjuvant Treatment for Women With High Risk Early Breast Cancer Receiving Neoadjuvant or Adjuvant Therapy (D-CARE) |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants With a CV (or Unknown) Death, Based on Contemporary Endpoint Definitions | 88 of 2,220 96 of 2,227 | -0.3 points -1.5 to 0.8 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants (Par.) With an Event of Stroke (Fatal and Non-fatal), Based on Original RECORD Endpoint Definitions | 50 of 2,220 63 of 2,227 | -0.6 points -1.5 to 0.4 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants With a CV (or Unknown) Death, Based on Original RECORD Endpoint Definitions | 88 of 2,220 96 of 2,227 | -0.3 points -1.5 to 0.8 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants With an Event of Myocardial Infarction (Fatal and Non-fatal), Based on Original RECORD Endpoint Definitions | 68 of 2,220 60 of 2,227 | 0.4 points -0.6 to 1.4 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants With a First Occurrence of a Major Adverse Cardiovascular Event (MACE) Defined as CV (or Unknown) Death, Non-fatal MI, and Non-fatal Stroke Based on Contemporary Endpoint Definitions | 186 of 2,220 191 of 2,227 | -0.2 points -1.8 to 1.4 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication (IR) Outcome: Number of Participants With a First Occurrence of a Major Adverse Cardiovascular Event (MACE) Defined as CV (or Unknown) Death, Non-fatal MI, and Non-fatal Stroke Based on Original RECORD Endpoint Definitions | 181 of 2,220 188 of 2,227 | -0.3 points -1.9 to 1.3 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Number of Participants With Cardiovascular Death/Cardiovascular Hospitalisation Events | 321 of 2,220 323 of 2,227 | -0.0 points -2.1 to 2.0 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants With an Event of Myocardial Infarction (Fatal and Non-fatal), Based on Contemporary Endpoint Definitions | 72 of 2,220 62 of 2,227 | 0.5 points -0.6 to 1.5 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants Who Died Due to Any Cause | 139 of 2,220 160 of 2,227 | -0.9 points -2.4 to 0.6 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Combined RSG vs Combined MET/SU: Independent Re-adjudication Outcome: Number of Participants With an Event of Stroke (Fatal and Non-fatal), Based on Contemporary Endpoint Definitions | 53 of 2,220 64 of 2,227 | -0.5 points -1.4 to 0.5 | 4,447 | NCT00379769 RECORD: Rosiglitazone Evaluated for Cardiac Outcomes and Regulation of Glycaemia in Diabetes |
| Universal PrEP Counselling vs Targeted PrEP Clinics: Appropriate PrEP Decision | 1,535 of 2,250 1,299 of 2,197 | 9.1 points 6.3 to 11.9 | 4,447 | NCT03070600 PrEP Implementation for Mothers in Antenatal Care |
| Universal PrEP Counselling vs Targeted PrEP Clinics: PrEP Acceptance | 441 of 2,250 387 of 2,197 | 2.0 points -0.3 to 4.3 | 4,447 | NCT03070600 PrEP Implementation for Mothers in Antenatal Care |
Code
curl "https://conductscience.org/api/comparisons/v1?page=99"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=99
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00141102-3926df21",
"title": "Celecoxib vs Oral Diclofenac Plus Omeprazole: Number of Subjects With SUs",
"summary": "5 of 2238 against 11 of 2246; risk difference -0.3 points, 95% interval -0.7 to 0.1; NCT00141102, Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis",
"record": "/library/comparisons/NCT00141102-3926df21",
"nct_id": "NCT00141102",
"kind": "outcome",
"participants": 4484,
"risk_difference": {
"value": -0.00266345810285707,
"lower": -0.006721778351325638,
"upper": 0.001021741198921569
},
"group_1": "5 of 2,238",
"group_2": "11 of 2,246",
"difference": "-0.3 points",
"interval": "-0.7 to 0.1",
"trial_title": "Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis"
},
{
"id": "NCT00141102-46da923d",
"title": "Celecoxib vs Oral Diclofenac Plus Omeprazole: Number of Subjects With CSULGIES or Symptomatic Ulcers (SUs)",
"summary": "25 of 2238 against 92 of 2246; risk difference -3.0 points, 95% interval -3.9 to -2.1; NCT00141102, Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis",
"record": "/library/comparisons/NCT00141102-46da923d",
"nct_id": "NCT00141102",
"kind": "outcome",
"participants": 4484,
"risk_difference": {
"value": -0.02979102159175641,
"lower": -0.039491980975307844,
"upper": -0.020671851264973524
},
"group_1": "25 of 2,238",
"group_2": "92 of 2,246",
"difference": "-3.0 points",
"interval": "-3.9 to -2.1",
"trial_title": "Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis"
}
],
"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=100",
"request_id": "uYuXNJbS15SpLcVN"
}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
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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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