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Impact of postoperative cognitive function after sevoflurane- or propofol-aneasthesia in elder cancer patients: a double-blinded randomized controlled trial

Impact of postoperative cognitive function after sevoflurane- or propofol-aneasthesia in elder cancer patients: a double-blinded randomized controlled trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-IOR-16009851
Enrollment
Unknown
Registered
2016-11-14
Start date
2016-11-07
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 cognitive dysfunction

Interventions

propofol group:propofol
control group:none

Sponsors

Guangxi Medical University Affiliated Tumor Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
65 Years to 85 Years

Inclusion criteria

Inclusion criteria: 1. The eligible patients were aged at least 65 years and less than 86 years, no matter sexuality and nationality; 2. The elderly will present for major abdominal malignant tumor resection under general anaesthesia, and estimated duration of operation is more than 2 hours 3. The aged with primary malignant tumor; 4. The patients and their consignors participate in this study and sign informed consents.

Exclusion criteria

Exclusion criteria: 1. Refuse to join the study; 2. History of depression, schizophrenia, epilepsy, Parkinsons disease, or myasthenia gravis; 3. Have serious Alzheimers disease, any severe visual or auditory disorders, were unable to understand the language used, coma, end-stage diseases and so forth; 4. Emergency operation 5. In a critical condition (the ASA classification before operation is IV or V; 6. History of neurological surgery; 7. MMSE<24, A score on the mini-mental state examination (MMSE) at screening of 23 or less; 8. History of alcoholism, or drug dependence.

Design outcomes

Primary

MeasureTime frame
incidence of postoperative cognitive dysfunction at 7th day after surgrry;incidence of postoperative cognitive dysfunction at 3 month after surgery;

Secondary

MeasureTime frame
Quality of recovery;the incidence of complication after surgery;length of stay in hospital after surgery;all-cause mortality;EORCT QLQ-C30;

Countries

China

Contacts

Public ContactLING-HUI PAN

Guangxi Medical University Affiliated Tumor Hospital

plinghui@hotmail.com+86 13807808637

Outcome results

None listed

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