Skip to content

Effects of dexmedetomidine on the incidence of postoperative delirium in critically ill elderly patients

Effects of dexmedetomidine on the incidence of postoperative delirium in critically ill elderly patients: a multicenter, prospective, randomized controlled trial

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-10000802
Enrollment
Unknown
Registered
2010-03-18
Start date
2011-08-01
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

postoperative delirium in critically ill elderly patients

Interventions

B:General anesthesia will be induced and maintained during surgery. Patient controlled analgesia will be provided for postoperative analgesia whenever necessary. Sedation level will be assessed with R
Dexmedetomidine group :General anesthesia will be provided during surgery and patient-controlled analgesia will be provided for postoperative analgesia in the same way as those in the placebo group.

Sponsors

Peking University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
Male
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Elderly patients (age >=65 years); 2. Planning to undergo elective noncardiac surgery under general anesthesia; 3. Admitted to ICU after surgery before 8:00 pm.

Exclusion criteria

Exclusion criteria: 1. Refuse to participate; 2. Preoperative history of schizophrenia, epilepsy, parkinsonism or myasthenia gravis; 3. Inability to communicate in the preoperative period because of coma, profound dementia or language barrier; 4. Brain injury or neurosurgery; 5. Preoperative left ventricular ejection fraction <30%, sick sinus syndrome, severe sinus bradycardia (<50 beats per minute), or second-degree or above atrioventricular block without pacemaker; 6. Severe hepatic dysfunction (Child-Pugh class C); 7. Severe renal dysfunction (requirement of renal replacement therapy before surgery); 8. Those who are unlikely to survive for more than 24 hours after surgery; 9. Other reasons that were considered unsuitable for study participation.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative delirium within the first seven days after surgery;

Secondary

MeasureTime frame
Postoperative all cause 30-day mortality;Incidence of postoperative non-delirium complications (during hospitalization or until 30 days after surgery);Duration of mechanical ventilation, length of stay in the ICU and hospital after surgery;

Countries

China

Contacts

Public ContactWang Dongxin
wangdongxin@hotmail.com+86 010 83575138

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 12, 2026