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85,013 comparisons from ClinicalTrials.gov.
Most participants first33,758 with no events in either group come last2,081 to 2,100 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| All TNFi Initiators Combination vs Tofacitinib Initiators Combination: Number of Participants With mACR20 at 6 Months for Tofacitinib Combination With MTX vs TNFi Combination With MTX | 1,224 of 4,013 19 of 90 | 9.4 points -0.2 to 16.7 | 4,103 | NCT05576051 To Estimate the Efficacy of Treatment With TNFi as Monotherapy or Combination Therapy With MTX and Compare and Contrast Efficacy With Tofacitinib as Monotherapy and Combination Therapy in a Real World Setting. |
| Celecoxib vs Oral Diclofenac Plus Omeprazole: Number of Subjects Hospitalized in Last 6 Months at the Post Trial Interview | 82 of 2,047 79 of 2,048 | 0.1 points -1.1 to 1.4 | 4,095 | 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 Alive at the Post Trial Interview | 2,018 of 2,047 2,023 of 2,048 | -0.2 points -0.9 to 0.5 | 4,095 | NCT00141102 Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis |
| Interactive Two-way SMS Dialogue vs No SMS Control: Initiation of Early Breastfeeding | 1,510 of 2,088 1,402 of 2,007 | 2.5 points -0.3 to 5.2 | 4,095 | NCT04598165 Mobile WACh NEO: Mobile Solutions for Neonatal Health and Maternal Support |
| Telepharmacist Intervention vs Usual Care: Healthcare Utilization - Hospitalizations | 170 of 2,038 156 of 2,040 | 0.7 points -1.0 to 2.4 | 4,078 | NCT02512276 Tele-Pharmacy Intervention to Improve Treatment Adherence |
| Telepharmacist Intervention vs Usual Care: Healthcare Utilization - ER Visits | 90 of 2,038 113 of 2,040 | -1.1 points -2.5 to 0.2 | 4,078 | NCT02512276 Tele-Pharmacy Intervention to Improve Treatment Adherence |
| Telepharmacist Intervention vs Usual Care: Healthcare Utilization - Office Visits | 641 of 2,038 594 of 2,040 | 2.3 points -0.5 to 5.2 | 4,078 | NCT02512276 Tele-Pharmacy Intervention to Improve Treatment Adherence |
| Mortality Pre-TIF Introduction vs Mortality Post-TIF Introduction: Mortality | 47 of 2,067 22 of 2,010 | 1.2 points 0.4 to 2.0 | 4,077 | NCT04547192 Improving Initial Management of the Injured at Ghanaian District and Regional Hospitals With a Trauma Intake Form |
| Mortality Pre-TIF Introduction vs Mortality Post-TIF Introduction: deaths from any cause | 47 of 2,067 22 of 2,010 | 1.2 points 0.4 to 2.0 | 4,077 | NCT04547192 Improving Initial Management of the Injured at Ghanaian District and Regional Hospitals With a Trauma Intake Form |
| Mortality Pre-TIF Introduction vs Mortality Post-TIF Introduction: serious adverse events | 24 of 2,067 6 of 2,010 | 0.9 points 0.3 to 1.4 | 4,077 | NCT04547192 Improving Initial Management of the Injured at Ghanaian District and Regional Hospitals With a Trauma Intake Form |
| Positive Berlin Questionaires vs Negative Berlin Questionnaires: Diagnosis of Pre-eclampsia Among Subjects With Positive Berlin Questionnaires | 135 of 1,343 49 of 2,731 | 8.3 points 6.7 to 10.0 | 4,074 | NCT00462306 Incidence of Obstructive Sleep Apnea in Pregnancy |
| Rapid HIV Testing w/ Counseling (Group 1) vs Rapid HIV Testing & Information Only (Group 2): STI Incidence | 250 of 2,039 226 of 2,032 | 1.1 points -0.8 to 3.1 | 4,071 | NCT01154296 HIV Rapid Testing & Counseling in Sexually Transmitted Disease (STD) Clinics in the U.S. |
| Active Antihypertensive Treatment vs Usual Care: A Combination of Death Within 14 Days After Randomization and Major Disability at 14 Days or at Hospital Discharge if Earlier Than 14 Days. | 683 of 2,038 681 of 2,033 | 0.0 points -2.9 to 2.9 | 4,071 | NCT01840072 China Antihypertensive Trial in Acute Ischemic Stroke |
| Treatment - Participation in Nurse Family Partnership vs Control: Number of Participants With a Tdap Vaccination (27-36 Weeks) | 914 of 2,723 446 of 1,347 | 0.5 points -2.6 to 3.5 | 4,070 | NCT03360539 Nurse-Family Partnership Impact Evaluation in South Carolina |
| High Dose Multivitamin vs Low Dose Multivitamin: Recurrent or de Novo Arteriosclerotic Cardiovascular Disease (CVD) Defined as the Occurrence of Non-fatal or Fatal Arteriosclerotic Outcomes Including Coronary Heart, Cerebrovascular, and Peripheral Vascular Disease Events | 269 of 2,029 278 of 2,029 | -0.4 points -2.5 to 1.7 | 4,058 | NCT00064753 Folic Acid for Vascular Outcome Reduction In Transplantation (FAVORIT) |
| High Dose Multivitamin vs Low Dose Multivitamin: Renal Graft Failure | 181 of 2,029 162 of 2,029 | 0.9 points -0.8 to 2.7 | 4,058 | NCT00064753 Folic Acid for Vascular Outcome Reduction In Transplantation (FAVORIT) |
| With BPH vs Without BPH: Risk Factors for Incidence Rate of Treatment Related Adverse Events (TRAEs) of Tolterodine - Comorbidity of Prostatic Hypertrophy | 319 of 2,203 130 of 1,855 | 7.5 points 5.6 to 9.3 | 4,058 | NCT01488578 Tolterodine Drug Use Investigation.(Post Marketing Commitment Plan) |
| qHPV Vaccine in Base Study vs Placebo in Base Study: Base Study: Number of Participants With Severe Injection Site Adverse Experiences (AEs) | 25 of 2,020 20 of 2,029 | 0.3 points -0.4 to 0.9 | 4,049 | NCT00090285 An Investigational Study of Gardasil™ (qHPV Vaccine) in Reducing the Incidence of Anogenital Warts in Young Men (V501-020) |
| GSK2340274A Group vs GSK2340273A Group: deaths from any cause | 6 of 2,025 1 of 2,023 | 0.2 points -0.0 to 0.6 | 4,048 | NCT00979602 Safety, Immunogenicity, and Relative Efficacy of H1N1 Vaccines in Adults Aged 18 Years and Older |
| GSK2340274A Group vs GSK2340273A Group: serious adverse events | 84 of 2,025 73 of 2,023 | 0.5 points -0.7 to 1.7 | 4,048 | NCT00979602 Safety, Immunogenicity, and Relative Efficacy of H1N1 Vaccines in Adults Aged 18 Years and Older |
Code
curl "https://conductscience.org/api/comparisons/v1?page=105"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=105
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT05576051-8923d4e6",
"title": "All TNFi Initiators Combination vs Tofacitinib Initiators Combination: Number of Participants With mACR20 at 6 Months for Tofacitinib Combination With MTX vs TNFi Combination With MTX",
"summary": "1224 of 4013 against 19 of 90; risk difference 9.4 points, 95% interval -0.2 to 16.7; NCT05576051, To Estimate the Efficacy of Treatment With TNFi as Monotherapy or Combination Therapy With MTX and Compare and Contrast Efficacy With Tofacitinib as Monotherapy and Combination Therapy in a Real World Setting.",
"record": "/library/comparisons/NCT05576051-8923d4e6",
"nct_id": "NCT05576051",
"kind": "outcome",
"participants": 4103,
"risk_difference": {
"value": 0.09389761054351134,
"lower": -0.0023704847397606754,
"upper": 0.16692187106859988
},
"group_1": "1,224 of 4,013",
"group_2": "19 of 90",
"difference": "9.4 points",
"interval": "-0.2 to 16.7",
"trial_title": "To Estimate the Efficacy of Treatment With TNFi as Monotherapy or Combination Therapy With MTX and Compare and Contrast Efficacy With Tofacitinib as Monotherapy and Combination Therapy in a Real World Setting."
},
{
"id": "NCT00141102-278f4495",
"title": "Celecoxib vs Oral Diclofenac Plus Omeprazole: Number of Subjects Hospitalized in Last 6 Months at the Post Trial Interview",
"summary": "82 of 2047 against 79 of 2048; risk difference 0.1 points, 95% interval -1.1 to 1.4; NCT00141102, Study Of Celecoxib Or Diclofenac And Omeprazole For Gastrointestinal (GI) Safety In High GI Risk Patients With Arthritis",
"record": "/library/comparisons/NCT00141102-278f4495",
"nct_id": "NCT00141102",
"kind": "outcome",
"participants": 4095,
"risk_difference": {
"value": 0.0014844036242061542,
"lower": -0.010524506321263751,
"upper": 0.013511999897525575
},
"group_1": "82 of 2,047",
"group_2": "79 of 2,048",
"difference": "0.1 points",
"interval": "-1.1 to 1.4",
"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=106",
"request_id": "vYsdORSFh8Xar2hL"
}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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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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