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Effects of dexmedetomidine on perioperative stress response and postoperative recovery in elderly patients undergoing thoracoscopic surgery

Effects of dexmedetomidine on perioperative stress response and postoperative recovery in elderly patients undergoing thoracoscopic surgery

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000039478
Enrollment
Unknown
Registered
2020-10-29
Start date
2020-11-01
Completion date
Unknown
Last updated
2021-02-01

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

Conditions

Lung disease

Interventions

dexmedetomidine group:Intravenous infusion of dexmedetomidine (0.8 g·kg-1·h-1) for 10min before anesthesia induction, followed by continuous infusion at a rate of 0.4 g·kg-1·h-1 for 30min before the e
lidocaine group:Intravenous lidocaine 1.0mg·kg-1·h-1 was injected before anesthesia induction for 10min, and then the infusion was continued at a rate of 1mg·kg-1·h-1 for 30min before the end of the o
control group:Before anesthesia induction, normal saline was injected intravenously for 10min, and then the infusion was continued at the rate of 1mg·kg-1·h-1 for 30min before the end of the operation

Sponsors

Department of Anesthesia, the First Affiliated Hospital of Chongqing Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. All patients had unilateral lobar tumors with tumor diameter < 5 cm; 2. Optional thoracoscopic radical resection of lung cancer under general anesthesia; 3. No other complications before surgery, no history of radiotherapy and chemotherapy; 4. Age 65~80 years old, regardless of gender, BMI <= 30 kg/m2; 5. According to the New York Heart Association (NYHA) classification, cardiac function grade I~II; 6. Patients volunteered to participate in this study and signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Non-thoracoscopic lobectomy; 2. Operation time > 5 hours; 3. Sinus bradycardia or atrioventricular block; 4. the past use of immunosuppressants and recent chemoradiotherapy; 5. Local anesthetic allergy; 6. Liver and kidney dysfunction; 7. Diabetes; 8. Epilepsy and accompanied by mental, cognitive dysfunction and long-term stress stimulation or psychological disorders; 9. Blood transfusion patients; 10. Patients taking non-steroidal anti-inflammatory or steroid drugs, angiotensin-converting enzyme inhibitors, or bronchodilators.

Design outcomes

Primary

MeasureTime frame
Plasma cortisol, adrenaline, norepinephrine, IL-6, TNF-a, C-reactive protein;Short-term postoperative prognosis;

Countries

China

Contacts

Public ContactKe Wei

The First Affiliated Hospital of Chongqing Medical University

wk202448@hospital-cqmu.com+86 15902360621

Outcome results

None listed

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