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Clinical Trials/NCT02766062
NCT02766062
Completed
Not Applicable

Effects of Propofol and Sevoflurane on Early Postoperative Cognitive Dysfunction in Elderly Patients With Metabolic Syndrome

General Hospital of Ningxia Medical University0 sites94 target enrollmentSeptember 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Postoperative Complications
Sponsor
General Hospital of Ningxia Medical University
Enrollment
94
Primary Endpoint
Number of participants with Postoperative cognitive dysfunction (POCD) as assessed by Mini-Mental State Examination (MMSE) score in propofol group and sevoflurane group
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to investigate propofol versus sevoflurane anesthesia on the effects of early postoperative cognitive function in elderly patients with metabolic syndrome.

Detailed Description

By now, a series risk factors of cardiovascular diseases, which are also related to the development of postoperative cognitive dysfunction (POCD), are becoming more common.The investigators don't know whether propofol based anesthesia has a more severe impact on early postoperative cognitive function than sevoflurane in elderly patients with metabolic syndrome. In this study, the investigators want to investigate propofol versus sevoflurane anesthesia on the effects of early postoperative cognitive function in elderly patients with metabolic syndrome.

Registry
clinicaltrials.gov
Start Date
September 2015
End Date
May 2016
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
General Hospital of Ningxia Medical University
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • aged ≥60 years;
  • noncardiac surgery and nonneural surgery

Exclusion Criteria

  • Mini Mental State Examination \[MMSE\] score too low
  • chronic alcoho and drug abuse
  • disturbed renal and liver function
  • history of a cerebrovascular accident
  • permanent ventricular pacing
  • preoperative cognitive deficits
  • lack of cooperation

Outcomes

Primary Outcomes

Number of participants with Postoperative cognitive dysfunction (POCD) as assessed by Mini-Mental State Examination (MMSE) score in propofol group and sevoflurane group

Time Frame: up to 7days postoperatively

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