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The effect of cyclopofol on the circulatory variability of painless gastrointestinal endoscopy and early postoperative cognitive function in elderly patients with different frailty

The effect of cyclopofol on the circulatory variability of painless gastrointestinal endoscopy and early postoperative cognitive function in elderly patients with different frailty

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2600119738
Enrollment
Unknown
Registered
2026-03-03
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-09

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

Conditions

Frailty in elderly patients

Interventions

Sponsors

Suining Central Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to No maximum

Inclusion criteria

Inclusion criteria: 1. Age >= 65 years; 2. Scheduled for routine painless gastrointestinal endoscopy at Suining Central Hospital; 3. Undergoing intravenous sedation anesthesia with propofol or ciprofol; 4. Able to complete preoperative cognitive assessment (MMSE = 23); 5. Complete perioperative monitoring data (mean arterial pressure, heart rate, SpO2, etc.); 6. Informed consent was obtained from the patient and their family members;

Exclusion criteria

Exclusion criteria: 1. Severe organic diseases (e.g., NYHA Class III or above heart failure, unstable angina, recent myocardial infarction within 3 months, severe COPD, severe liver/kidney dysfunction; 2. History of moderate/severe cognitive impairment, psychiatric disorders, or inability to complete cognitive assessment. 3. Preoperative acute conditions affecting circulatory stability (e.g., infection, high fever, electrolyte disorders). 4. Incomplete anesthesia or monitoring data, missing key parameters (e.g., BP, HR, SpO2). 5. Serious intraoperative adverse events resulting in unusable data; 6. Refusal to provide informed consent or withdrawal from the study during participation.

Design outcomes

Primary

MeasureTime frame
Mean arterial pressure variability (?MAP);

Secondary

MeasureTime frame
Intraoperative Vital Signs Changes;Recovery Time from Anesthesia (Including Awakening Time and Discharge Time);Incidence of Postoperative Adverse Events;Number Cancellation Test, NCT;Postoperative Cognitive Function;

Countries

China

Contacts

Public ContactJinping Wang

Suining Central Hospital

404060921@qq.com+86 825 229 2250

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Mar 14, 2026