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Effects of cyclopolfol and propofol on delirium after laparoscopic major abdominal surgery in elderly patients

Effects of cyclopolfol and propofol on delirium after laparoscopic major abdominal surgery in elderly patients

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107710
Enrollment
Unknown
Registered
2025-08-18
Start date
2025-08-25
Completion date
Unknown
Last updated
2025-08-25

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

Conditions

major abdominal surgery

Interventions

Cyclopofol group:Anesthesia was induced and maintained with cyclopropofol
Propofol group:Anesthesia was induced and maintained with propofol

Sponsors

Affiliated Hospital of North Sichuan Medical College
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Age >65 years old, BMI value 18-30m^2/kg; 2. American society of anesthesiology (ASA) grade I~III; 3. CAM confirmed that there was no pre-existing delirium before surgery; 4. The score of the Mini-Mental State Examination Scale >=15 points.

Exclusion criteria

Exclusion criteria: 1. History of previous neurological or psychiatric diseases; 2. Long-term use of sedative, hypnotic and antipsychotic drugs; 3. Severe vision and hearing impairment; 4. BMI value less than 18 m^2/kg or greater than 30 m^2/kg; 5. Those who have dysfunction of important organs such as heart, lung, liver, and kidney.

Design outcomes

Primary

MeasureTime frame
Incidence and duration of POD (within 7 days after surgery);

Secondary

MeasureTime frame
Record the unit time dosage of propofol, propofol, and remifentanil during anesthesia maintenance, as well as the use of related drugs (atropine, methoxamine, norepinephrine, dopamine) during surgery;Quality of awakening;hemodynamics;SII value;

Countries

China

Contacts

Public ContactYujiao Yang

Department of Anesthesiology, Affiliated Hospital of North Sichuan Medical College

yangyujiao@nsmc.edu.cn+86 182 8170 1382

Outcome results

None listed

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