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 last4,981 to 5,000 of 85,013
| Comparison | With the outcome | Risk difference, 95% interval | Participants | Trial |
|---|---|---|---|---|
| H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: deaths from any cause | 1 of 961 0 of 245 | 0.1 points -1.4 to 0.6 | 1,206 | NCT00449670 Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults |
| H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: serious adverse events | 25 of 961 5 of 245 | 0.6 points -2.2 to 2.2 | 1,206 | NCT00449670 Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults |
| Clinically Driven Monitoring (CDM) vs Laboratory Plus Clinical Monitoring (LCM): LCM vs CDM: New Grade 3 or 4 Adverse Event (AE), Not Solely Related to HIV | 283 of 606 282 of 600 | -0.3 points -5.9 to 5.3 | 1,206 | NCT02028676 Efficacy Study of Different Laboratory Management Strategies and Drug Regimens in HIV-infected Children in Africa |
| Clinically Driven Monitoring (CDM) vs Laboratory Plus Clinical Monitoring (LCM): LCM vs CDM: Disease Progression to a New WHO Stage 4 Event or Death | 47 of 606 39 of 600 | 1.3 points -1.7 to 4.2 | 1,206 | NCT02028676 Efficacy Study of Different Laboratory Management Strategies and Drug Regimens in HIV-infected Children in Africa |
| Clinically Driven Monitoring (CDM) vs Laboratory Plus Clinical Monitoring (LCM): LCM vs CDM, Induction ART: Cessation of First-line Regimen for Clinical/Immunological Failure | 28 of 606 35 of 600 | -1.2 points -3.8 to 1.3 | 1,206 | NCT02028676 Efficacy Study of Different Laboratory Management Strategies and Drug Regimens in HIV-infected Children in Africa |
| Acoziborole vs Placebo: Occurrence of TEAEs - Headache | 53 of 906 8 of 300 | 3.2 points 0.3 to 5.3 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of Serious TEAEs | 3 of 906 4 of 300 | -1.0 points -3.1 to 0.0 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Gastritis | 6 of 906 3 of 300 | -0.3 points -2.3 to 0.7 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Fatigue | 14 of 906 5 of 300 | -0.1 points -2.4 to 1.3 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of Adverse Events (AEs) | 195 of 906 69 of 300 | -1.5 points -7.2 to 3.7 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of Any Treatment-related TEAEs | 59 of 906 17 of 300 | 0.8 points -2.7 to 3.6 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Acarodermatitis | 13 of 906 3 of 300 | 0.4 points -1.6 to 1.6 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Nausea | 7 of 906 3 of 300 | -0.2 points -2.2 to 0.8 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Malaria | 34 of 906 14 of 300 | -0.9 points -4.1 to 1.4 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Abdominal Pain | 23 of 906 9 of 300 | -0.5 points -3.2 to 1.4 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Blood Potassium Increased | 8 of 906 6 of 300 | -1.1 points -3.5 to 0.3 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: deaths from any cause | 0 of 906 1 of 300 | -0.3 points -1.9 to 0.2 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of TEAEs - Enteritis | 7 of 906 4 of 300 | -0.6 points -2.6 to 0.6 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: Occurrence of Any TEAEs | 195 of 906 69 of 300 | -1.5 points -7.2 to 3.7 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
| Acoziborole vs Placebo: serious adverse events | 3 of 906 4 of 300 | -1.0 points -3.1 to 0.0 | 1,206 | NCT05256017 Safety and Tolerability Study of Acoziborole in g-HAT Seropositive Subjects |
Code
curl "https://conductscience.org/api/comparisons/v1?page=250"
Response
The first 2 of this page's 20 results. GET /api/comparisons/v1?page=250
{
"data": {
"total": 85013,
"results": [
{
"id": "NCT00449670-deaths",
"title": "H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: deaths from any cause",
"summary": "1 of 961 against 0 of 245; risk difference 0.1 points, 95% interval -1.4 to 0.6; NCT00449670, Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults",
"record": "/library/comparisons/NCT00449670-deaths",
"nct_id": "NCT00449670",
"kind": "deaths",
"participants": 1206,
"risk_difference": {
"value": 0.001040582726326743,
"lower": -0.014420554442176596,
"upper": 0.005870607850164397
},
"group_1": "1 of 961",
"group_2": "0 of 245",
"difference": "0.1 points",
"interval": "-1.4 to 0.6",
"trial_title": "Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults"
},
{
"id": "NCT00449670-sae",
"title": "H5N1 Adjuvanted Group vs H5N1 Un-adjuvanted Group: serious adverse events",
"summary": "25 of 961 against 5 of 245; risk difference 0.6 points, 95% interval -2.2 to 2.2; NCT00449670, Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults",
"record": "/library/comparisons/NCT00449670-sae",
"nct_id": "NCT00449670",
"kind": "serious-adverse-events",
"participants": 1206,
"risk_difference": {
"value": 0.005606404892862453,
"lower": -0.02214179846030292,
"upper": 0.02241526310445212
},
"group_1": "25 of 961",
"group_2": "5 of 245",
"difference": "0.6 points",
"interval": "-2.2 to 2.2",
"trial_title": "Assess Consistency of Immunogenicity of GlaxoSmithKline Biologicals' Pandemic Influenza Vaccine (GSK1562902A) in Adults"
}
],
"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": {
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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=251",
"request_id": "poyHlZTaWi9nthWW"
}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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GET https://conductscience.org/api/comparisons/v1?q=placebo%20heart%20failure&kind=outcome
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