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Perioperative Application of Liraglutide for the Prevention of Postoperative Delirium among Elderly Patients with Type 2 Diabetes Undergoing Cardiac Surgery: A Single-Center Randomized Controlled Study

Perioperative Application of Liraglutide for the Prevention of Postoperative Delirium among Elderly Patients with Type 2 Diabetes Undergoing Cardiac Surgery: A Single-Center Randomized Controlled Study

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083284
Enrollment
Unknown
Registered
2024-04-19
Start date
2024-04-30
Completion date
Unknown
Last updated
2024-04-22

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

Conditions

Postoperative Delirium

Interventions

Liraglutide Group:Subcutaneous injection of liraglutide: 0.6 mg administered the day before surgery, 1.8 mg administered post-anesthesia induction on the day of surgery, followed by 0.6 mg daily for t
Vehicle Group:Subcutaneous injection of vehicle: the same volume as liraglutide administrated at the corresponding times.

Sponsors

Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age = 60 years 2. Type 2 diabetes 3. Patients undergoing elective cardiac surgery

Exclusion criteria

Exclusion criteria: 1. History of neurological or psychiatric disorders, such as schizophrenia, epilepsy, Parkinson's disease, severe dementia, etc 2. Patients with communication difficulties, such as severe visual, auditory, or speech impairments 3. History of central nervous system damage or surgery 4. Cardiac function NYHA Class IV 5. Severe liver dysfunction (Child-Pugh Class C) 6. Severe renal failure requiring renal replacement therapy 7. History of pancreatitis 8. Type 1 diabetes 9. Patients whose blood sugar cannot be controlled within 4-8 mmol/L during the intervention period 10. Patients with medullary thyroid carcinoma or a family history of it 11. Pregnant or breastfeeding women 12. Intolerance or allergy to liraglutide 13. Previous use of GLP-1A and SGLT2i 14. Patients who refuse to sign the informed consent

Design outcomes

Primary

MeasureTime frame
The incidence of delirium within 7 days postoperatively;

Secondary

MeasureTime frame
The severity of delirium within 7 days postoperatively;Cognitive function at discharge, and at 3 months, 6 months, and 1 year postoperatively;Anxiety and depression at discharge, and at 3 months, 6 months, and 1 year postoperatively;Cardiac function at discharge, and at 3 months, 6 months, and 1 year postoperatively;Duration of ICU stay;Mechanical ventilation time;Duration of hospital stay ; In-hospital mortality;Incidence of adverse events during medication use;Rate of major cardiovascular adverse events within 1 year post-surgery (including cardiovascular death, myocardial infarction, and stroke);Serum levels of NSE;Serum levels of CRP;Serum levels of IL-1a;Serum levels of TNF-a;Serum levels of C3;Serum levels of LDH;Serum levels of CK;Serum levels of BNP;Serum levels of CK-MB;Serum levels of AST;Serum levels of cTNT;Serum levels of C1q;Serum levels of IL-1ß;Serum levels of IL-6;Serum levels of S100ß;

Countries

China

Contacts

Public ContactWenxue Liu

Nanjing Drum Tower Hospital, Affiliated Hospital of Medical School, Nanjing University

diligent_hi@163.com+86 157 5186 6806

Outcome results

None listed

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