Skip to content

The effect of different general anesthesia to the perioperative cerbral function of geriatric patients

The effect of different general anesthesia to the perioperative cerbral function of geriatric patients

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-13003789
Enrollment
Unknown
Registered
2013-10-14
Start date
2013-11-21
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

Lumbar spinal stenosis and/or lumbar intervertebral disc herniation and/or Gastrointestinal Tumor

Interventions

TIVA group(orthopedics):TIVA aesthesia
Intravenous-inhalation anesthesia group(orthopedics) :Intravenous-inhalation anesthesia
TIVA group (general surgery):TIVA
Intravenous-inhalation anesthesia group (general surgery):Intravenous-inhalation anesthesia

Sponsors

Department of Anesthesia, Third Hospital, Peking University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
60 Years to 90 Years

Inclusion criteria

Inclusion criteria: Older than 60 years and younger than 90 years of age, both genders, no race limitation; Receiving general anesthesia for elective abdominal or lumbar spine surgery, expected operation time longer than 2 hours; Agreed to participate in this study and signed an informed consent form.

Exclusion criteria

Exclusion criteria: Refused to participate in the study; A history of schizophrenia or epilepsy, Parkinson's medical history; due to severe dementia, language barriers, coma, end-stage disease, etc. can not be completed preoperative evaluation; Within 3 months before surgery had myocardial infarction; Severe heart, liver, kidney dysfunction: preoperative ASA classification higher than IV grade; serum creatinine more than 442 umol/L, with or without serum potassium more than 6.5 mmol/L, or clinician considers it necessary to line renal replacement therapy; Child -Pugh grade C; Researchers believe the attending physician or the presence of other conditions should not participate in this study; Allergic to the study medicines.

Design outcomes

Primary

MeasureTime frame
Perioperative cerebral functional status of patient;Intraoperative Doppler monitoring of cerebral blood flow;Cortisol;IL-6;

Contacts

Public ContactXiangyang Guo

Department of Anesthesia, Third Hospital, Peking University

puthmzk@163.com+86 13581961965

Outcome results

None listed

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