← Trials/Trial dossier/NCT06118203

Completed

Semaglutide Use in Acute Pulmonary Embolism

Evaluation of Circulating Endothelial Inflammatory Biomarkers in Response to GLP-1 Agonist Semaglutide in Acute Pulmonary Embolism

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

NCT IDNCT06118203
Org study ID300440

Timeline

Milestones

Study start2022-01-02actual
Primary completion2023-03-04actual
Study completion2023-03-05actual
Study first posted2023-11-07actual
Last update posted2026-03-27actual

Assets

Investigational agents

Study populations

Who this study enrolls

Cardiovascular disease

Eligibility

Who can enroll

Minimum age18 Years
Maximum age80 Years
SexAll
Healthy volunteersNot accepted
Sampling methodNon probability sample

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 endpoints
Primary/protocol endpoint/low confidence

Endothelial biomarker measurement

Time frame:4 weeks

change from baseline, improvement

Secondary/protocol endpoint

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

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 1, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableno registry results posted yet

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.