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 last4,061 to 4,080 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| Depressed in the ED vs Cognitively Impaired in the ED: Depression and Cognitive Impairment at 2 Weeks | 27 of 803 5 of 808 | 2.7 points 1.4 to 4.3 | 1,611 | NCT00717041 Epidemiology of Depression, Anxiety, and Cognitive Impairment |
| BuMA Supreme Coronary Stent System (ITT) vs Durable Polymer EES (XIENCE or Promus DES) (ITT): Procedure Success | 1,042 of 1,074 514 of 537 | 1.3 points -0.5 to 3.5 | 1,611 | NCT03168776 PIONEER III Trial to Assess Safety and Efficacy of the BuMA Supreme™ Drug Coated Coronary Stent in Patients With Coronary Disease |
| Rivaroxaban (Xarelto, BAY59-7939) vs Antiplatelet: Number of Participants With Death or First Thromboembolic Event (DTE) | 68 of 801 63 of 807 | 0.7 points -2.0 to 3.4 | 1,608 | NCT02556203 Global Study Comparing a rivAroxaban-based Antithrombotic Strategy to an antipLatelet-based Strategy After Transcatheter aortIc vaLve rEplacement to Optimize Clinical Outcomes |
| Rivaroxaban Arm vs Antiplatelet Arm: deaths from any cause | 70 of 801 43 of 807 | 3.4 points 0.9 to 6.0 | 1,608 | NCT02556203 Global Study Comparing a rivAroxaban-based Antithrombotic Strategy to an antipLatelet-based Strategy After Transcatheter aortIc vaLve rEplacement to Optimize Clinical Outcomes |
| Rivaroxaban Arm vs Antiplatelet Arm: serious adverse events | 296 of 801 282 of 807 | 2.0 points -2.7 to 6.7 | 1,608 | NCT02556203 Global Study Comparing a rivAroxaban-based Antithrombotic Strategy to an antipLatelet-based Strategy After Transcatheter aortIc vaLve rEplacement to Optimize Clinical Outcomes |
| Prophylactic NPWT vs Standard Dressing: Number of Participants With Skin Blistering, Erythema, Wound Bleeding (Measures of Adverse Skin Events) | 46 of 806 5 of 802 | 5.1 points 3.5 to 6.9 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Prophylactic NPWT vs Standard Dressing: Number of Participants With Superficial or Deep Surgical Site Infections (SSIs) | 29 of 806 27 of 802 | 0.2 points -1.6 to 2.1 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Prophylactic NPWT vs Standard Dressing: Number of Participants With Superficial, Deep or Organ Space SSIs (Individual Types of SSIs) | 29 of 806 27 of 802 | 0.2 points -1.6 to 2.1 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Prophylactic NPWT vs Standard Dressing: Number of Participants With a Composite of Any Wound Complication Including SSI, Hematoma, Seroma, Separation (2cm or More). | 52 of 806 54 of 802 | -0.3 points -2.7 to 2.2 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Prophylactic NPWT vs Standard Dressing: Number of Participants With Wound Hematoma, Seroma, Separation (Other Wound Complications) | 21 of 806 25 of 802 | -0.5 points -2.2 to 1.2 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Prophylactic NPWT vs Standard Dressing: Number of Participants With Organ Space SSIs (Endometritis, Intraabdominal Abscess) | 2 of 806 2 of 802 | -0.0 points -0.7 to 0.7 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Prophylactic NPWT vs Standard Dressing: Number of Participants With Physician Office Visit, Emergency Room Visit, Attendance at Wound Clinic, Use Antibiotics, Hospital Readmission for Wound Related Problems (Measures of Healthcare Resource Utilization) | 130 of 806 132 of 802 | -0.3 points -3.9 to 3.3 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Prophylactic NPWT vs Standard Dressing: serious adverse events | 4 of 806 5 of 802 | -0.1 points -1.0 to 0.7 | 1,608 | NCT03009110 Preventing Adverse Incisional Outcomes at Cesarean Multicenter Trial |
| Engerix-B® Hepatitis B Vaccination vs Sci-B-Vac® Hepatitis B Vaccination: serious adverse events | 21 of 811 32 of 796 | -1.4 points -3.3 to 0.3 | 1,607 | NCT03393754 Immunogenicity and Safety of Sci-B-Vac® to Engerix-B® in Adults |
| Treatment Group (Defined in Protocol as Pooled Intervention Group 1 and Intervention Group 2) vs Control Group: Number of Participants Who Developed a New Pressure Ulcer Category 2 or Worse on Any Heel | 15 of 1,066 10 of 539 | -0.4 points -2.1 to 0.8 | 1,605 | NCT03442777 Silicone Adhesive Multilayer Foam Dressings to Prevent Pressure Ulcer |
| Treatment Group (Defined in Protocol as Pooled Intervention Group 1 and Intervention Group 2) vs Control Group: The Number of Participants Who Developed a New Pressure Ulcer Category 2 or Worse on Any Trochanter | 1 of 1,066 0 of 539 | 0.1 points -0.6 to 0.5 | 1,605 | NCT03442777 Silicone Adhesive Multilayer Foam Dressings to Prevent Pressure Ulcer |
| Treatment Group (Defined in Protocol as Pooled Intervention Group 1 and Intervention Group 2) vs Control Group: Number of Participants Who Developed a New Pressure Ulcer Category 2 or Worse on Sacrum, Heels or Greater Trochanter | 43 of 1,066 34 of 539 | -2.3 points -4.9 to -0.1 | 1,605 | NCT03442777 Silicone Adhesive Multilayer Foam Dressings to Prevent Pressure Ulcer |
| Treatment Group (Defined in Protocol as Pooled Intervention Group 1 and Intervention Group 2) vs Control Group: Number of Participants Who Developed a New Pressure Ulcer Category 2 or Worse on Sacrum | 30 of 1,066 26 of 539 | -2.0 points -4.3 to -0.1 | 1,605 | NCT03442777 Silicone Adhesive Multilayer Foam Dressings to Prevent Pressure Ulcer |
| Massive Transfusion Protocol (RBCs, Plasma, Platelets, Whole Blood) vs Early Cryoprecipitate + Massive Transfusion Protocol (RBCs, Plasma, Platelets, Whole Blood): serious adverse events | 83 of 805 84 of 799 | -0.2 points -3.2 to 2.8 | 1,604 | NCT04704869 Early Use of Cryoprecipitate With Major Hemorrhage Protocol (MHP) Activation |
| Study 1a: Pharmacy-based PrEP Delivery Pilot (13 Months) vs Study 2: Pharmacy-based PrEP Delivery Pilot Extension (6 Months): PrEP Initiation | 287 of 575 661 of 1,028 | -14.4 points -19.4 to -9.3 | 1,603 | NCT04558554 Pharmacy Delivery to Expand the Reach of PrEP in Kenya |
Code
curl "https://conductscience.org/api/comparisons/v1?page=204"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=204
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00717041-e320f201",
"title": "Depressed in the ED vs Cognitively Impaired in the ED: Depression and Cognitive Impairment at 2 Weeks",
"summary": "27 of 803 against 5 of 808; risk difference 2.7 points, 95% interval 1.4 to 4.3; NCT00717041, Epidemiology of Depression, Anxiety, and Cognitive Impairment",
"record": "/library/comparisons/NCT00717041-e320f201",
"nct_id": "NCT00717041",
"kind": "outcome",
"participants": 1611,
"risk_difference": {
"value": 0.02743579152435792,
"lower": 0.014171279442235741,
"upper": 0.042707383170181856
},
"group_1": "27 of 803",
"group_2": "5 of 808",
"difference": "2.7 points",
"interval": "1.4 to 4.3",
"trial_title": "Epidemiology of Depression, Anxiety, and Cognitive Impairment"
},
{
"id": "NCT03168776-4c8b86e5",
"title": "BuMA Supreme Coronary Stent System (ITT) vs Durable Polymer EES (XIENCE or Promus DES) (ITT): Procedure Success",
"summary": "1042 of 1074 against 514 of 537; risk difference 1.3 points, 95% interval -0.5 to 3.5; NCT03168776, PIONEER III Trial to Assess Safety and Efficacy of the BuMA Supreme™ Drug Coated Coronary Stent in Patients With Coronary Disease",
"record": "/library/comparisons/NCT03168776-4c8b86e5",
"nct_id": "NCT03168776",
"kind": "outcome",
"participants": 1611,
"risk_difference": {
"value": 0.013035381750465591,
"lower": -0.005473762832930797,
"upper": 0.03537915955357974
},
"group_1": "1,042 of 1,074",
"group_2": "514 of 537",
"difference": "1.3 points",
"interval": "-0.5 to 3.5",
"trial_title": "PIONEER III Trial to Assess Safety and Efficacy of the BuMA Supreme™ Drug Coated Coronary Stent in Patients With Coronary Disease"
}
],
"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=205",
"request_id": "VI-jAC5C7efCv8Ow"
}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.
Patent publications
Paste a sequence and see the patents that disclose it.
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
Ask an assistant