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Semaglutide for Coronary Plaque Stabilization in Acute Coronary Syndromes with Type 2 Diabetes: A Randomized OCT Study (SEMPRESS Trial)

Semaglutide for Coronary Plaque Stabilization in Acute Coronary Syndromes with Type 2 Diabetes: A Randomized OCT Study (SEMPRESS Trial)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500106824
Enrollment
Unknown
Registered
2025-07-30
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-08-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Acute Coronary Syndromes with Type 2 Diabetes

Interventions

semaglutide treatment group:semaglutide treatment

Sponsors

Hebei General Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Males or females aged >=18 and 90°).

Exclusion criteria

Exclusion criteria: (1) Allergy or hypersensitivity to semaglutide. (2) Prior use of GLP-1 receptor agonists (GLP-1RA) before randomization. (3) Liver dysfunction (alanine aminotransferase >3× the upper limit of normal). (4) Renal dysfunction (creatinine clearance <45 mL/min). (5) Thrombocytopenia (platelet count <100 ×10?/L). (6) Uncontrolled infectious diseases. (7) Known immune-related diseases, including systemic lupus erythematosus, asthma, inflammatory bowel disease, gout, or malignancy. (8) Prior or planned systemic anti-inflammatory therapy, such as NSAIDs, corticosteroids, immunomodulators, or chemotherapy. (9) Surgery or interventional procedures within the past 6 months. (10) History of coronary artery bypass grafting (CABG) or planned CABG within 1 year. (11) Left main coronary artery disease (=50% lumen diameter reduction by angiography). (12) Severe coronary calcification or tortuosity deemed unsuitable for OCT assessment. (13) Psychiatric disorders (e.g., anxiety, depression). (14) Pregnancy, lactation, or women of childbearing potential not using effective contraception. (15) Participation in another clinical trial within the past 3 months. (16) Congenital heart disease without standardized treatment. (17) Life expectancy <1 year. (18) Investigator’s judgment of unsuitability for trial participation.

Design outcomes

Primary

MeasureTime frame
hsCRP;IL-1;IL-6;IL-18;IL-1ß;MPO;AZU1;Caspase-1CD86;CD206;oxLDL;TNFa;CD62L;MCP-1;ICAM-1;

Countries

China

Contacts

Public ContactDang Yi

Hebei General Hospital

dangyiemail@126.com+86 138 3119 8826

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026