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The effect of primary dyslipidemia on postoperative cognitive dysfunction in patients undergoing laparoscopic surgery

The effect of primary dyslipidemia on postoperative cognitive dysfunction in patients undergoing laparoscopic surgery

Status
Recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2100044287
Enrollment
Unknown
Registered
2021-03-14
Start date
2021-03-15
Completion date
Unknown
Last updated
2021-09-07

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

Conditions

postoperative cognitive dysfunction

Interventions

Sponsors

Guangxi Medical University Cancer Hospital
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 to 80 years old, without severe hearing or visual impairment, and able to read; 2. ASA grade I-II; 3. No history of heart, blood and brain related system diseases; 4. Plan to perform laparoscopic surgery under general anesthesia (except liver surgery), the operation time >= 2 hours; 5. The patient and the client agree to participate in this study.

Exclusion criteria

Exclusion criteria: 1. Patients with previous depression, severe dementia, schizophrenia, epilepsy, Parkinson's history, or myasthenia gravis, who cannot cooperate in the evaluation; 2. Heart function >= Grade 3, severe renal impairment (need kidney replacement Treatment), severe liver damage (Child-Pugh grade C); 3. Have a history of craniocerebral surgery; 4. Preoperative MMSE<23 points; 5. Intraoperative hemodynamics is unstable, and the mean arterial pressure exceeds the baseline fluctuation range +/- 25% for 3 minutes; 6. Secondary hyperlipidemia.

Design outcomes

Primary

MeasureTime frame
Cognitive function;

Countries

China

Contacts

Public ContactLin Fei

Guangxi Medical University Cancer Hospital

flylin0208@163.com+86 13707886172

Outcome results

None listed

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