Skip to content

Effect of remimazolam tosilate compared with propofol on perioperative neurocognitive disorders and prognosis in elderly patients after VATS

Effect of remimazolam tosilate compared with propofol on perioperative neurocognitive disorders and prognosis in elderly patients after VATS

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2200064657
Enrollment
Unknown
Registered
2022-10-13
Start date
2022-10-15
Completion date
Unknown
Last updated
2023-05-15

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

Conditions

Perioperative neurocognitive disorder

Interventions

Remimazolam tosilate group:Total intravenous anesthesia with remimazolam tosilate
Propofol group:Total intravenous anesthesia with propofol

Sponsors

National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 90 Years

Inclusion criteria

Inclusion criteria: 1. Male and female patients aged between 65 and 90 years old; 2. ASA physical status I-III; 3. Scheduled to undergo uniportal video-assisted thoracic surgery (VATS) lobectomy with expected duration of 2 hours to 4 hours, and an anticipated hospital stay of at least 5 days; 4. Body-mass index (BMI) between 18 and 27.9 kg/m2.

Exclusion criteria

Exclusion criteria: 1. Diagnosis of severe respiratory, cardiovascular, renal or hepatic dysfunction before surgery; 2. Hemoglobin < 90 g/L; 3. Had a history of stroke or any other central nervous system disease within 6 months; 4. Had a history of schizophrenia, epilepsy, Parkinsonism, myasthenia gravis or other mental illness; 5. Alcoholism or history of psychotropic substance dependence; 6. Inability to communicate because of severe visual, auditory or verbal problems; 7. Allergies or contraindications to propofol or benzodiazepines; 8. The Mini-Mental State Examination (MMSE) score <24 or delirium existed evaluated by confusion assessment method (CAM) 3 min diagnostic interview (3D-CAM) at baseline; 9. Receive radiotherapy, chemotherapy or immunotherapy; 10. Participated in other drug trials within 1 preoperative month.

Design outcomes

Primary

MeasureTime frame
Incidence of postoperative delirium within 5 days;

Secondary

MeasureTime frame
Onset time and duration of delirium;Cognitive function within 30 days after surgery;Cognitive function within 1 year after surgery;Postoperative analgesia within 5 days;Postoperative recovery;Related inflammatory biomarkers;Postoperative chronic pain within 3 months;

Countries

China

Contacts

Public ContactYan Tao

National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College

blizzardyt@163.com+86 13522553375

Outcome results

None listed

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