About this trial
Along with aging population, cancer incidence and mortality are increasing. However, despite advances in oncology and surgery, long-term survival of cancer patients is far from optimal. Dexmedetomidine is a highly selective alpha 2 adrenergic receptor agonist with sedative, analgesic, and anxiolytic effects. Studies showed that perioperative use of dexmedetomidine reduces delirium and some non-delirium complications after surgery. In long-term follow-up studies of older patients who, for other reasons, were randomized to receive either dexmedetomidine or placebo during intra- or postoperative period, dexmedetomidine use was associated with improved long-term survival. This multicenter randomized trial aims to investigate the effect of perioperative dexmedetomidine on long-term outcomes in older patients undergoing cancer surgery.
Eligibility criteria
Qualifiers
Aged 60 years or older.
Scheduled to undergo radical surgery for cancer under general anesthesia, with an expected surgical duration of 2 hours or longer.
Required patient-controlled intravenous analgesia after surgery.
Disqualifiers
Inability to communicate preoperatively due to visual, auditory, verbal. or other reasons.
Surgery for breast cancer or intracranial tumor.
Preoperative severe sinus bradycardia (<50 beats per minute), sick sinus syndrome,or second-degree or above atrioventricular block without pacemaker.
Severe hepatic dysfunction (Child-Pugh class C).
Trial design
Treatments tested in this trial
- Dexmedetomidine
- Placebo
Treatment groups
Sponsors and collaborators
Peking University First Hospital
Lead sponsor
Peking University
Collaborator