FindTrial
Sign In

Anesthesia under different way abdominal surgery patients of cognitive function after surgery for comparison

Anesthesia under different way abdominal surgery patients of cognitive function after surgery for comparison

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-12002345
Enrollment
Unknown
Registered
2012-07-17
Start date
2012-03-31
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:Propofol joint Remifentanil
Sevoflurane:Sevoflurane joint Remifentanil

Sponsors

The Second Affiliated Hospital of Harbin Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 99 Years

Inclusion criteria

Inclusion criteria: Older than 60 years old ASA II-III elective abdominal surgery patients

Exclusion criteria

Exclusion criteria: Liver and kidney function damage, mental illness, nervous system diseases, severe vision problems, serious hearing obstacles, illiteracy or alcohol abuse, use cold medication, etc.

Design outcomes

Primary

MeasureTime frame
Score of MMs;—

Countries

China

Contacts

Public ContactChun-Yu Song
scy-zw@163.com+86 18944614216

Outcome results

None listed

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