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Semaglutide Use in Acute Pulmonary Embolism
Evaluation of Circulating Endothelial Inflammatory Biomarkers in Response to GLP-1 Agonist Semaglutide in Acute Pulmonary Embolism
Lead sponsor
Assets
GLP-1 / incretin class catch-all / Semaglutide
Listed sites
1
Recruiting sites
—
Enrollment
18
actual
Study population
Cardiovascular disease
Key I/E criterion
—
Primary endpoint
•Endothelial biomarker measurement
Footprint
Where this trial recruits
Site locations as reported to ClinicalTrials.gov. Site count is not enrollment count; per-site enrollment is not available from source.
Identifiers
Registered as
Timeline
Milestones
Assets
Investigational agents
Study populations
Who this study enrolls
Eligibility
Who can enroll
Study population text
Acute admission with acute pulmonary embolism
Inclusion criteria
Acute pulmonary embolism
Exclusion criteria
Concurrent use of GLP-1 agonist
Endpoints (2)
What's being measured
Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.
Other (unclassified)
2 endpointsEndothelial biomarker measurement
Time frame:4 weeks
change from baseline, improvement
Plasma proteomics
Time frame:4 weeks
descriptive
Publications (1)
Bibliography
Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.
Registry references + supporting bibliography
- European heart journal open2026 Jan (month)PMID41536961doi:10.1093/ehjopen/oeaf170via clinicaltrials gov reference derived + pubmed nct search
Provenance
Sources
Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 1, 2026 snapshot.