Effects of Propofol and Sevoflurane on Early POCD in Elderly Patients With Metabolic Syndrome

NCT ID: NCT02766062

Last Updated: 2016-06-30

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

94 participants

Study Classification

INTERVENTIONAL

Study Start Date

2015-09-30

Study Completion Date

2016-05-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Postoperative Complications

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

Postoperative cognitive dysfunction metabolic syndrome propofol sevoflurane

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

propofol group

Patients with metabolic syndrome were randomly assigned to receive propofol anesthesia

Group Type ACTIVE_COMPARATOR

metabolic syndrome

Intervention Type OTHER

metabolic syndrome

sevoflurane group

Patients with metabolic syndrome were randomly assigned to receive sevoflurane anesthesia

Group Type ACTIVE_COMPARATOR

metabolic syndrome

Intervention Type OTHER

metabolic syndrome

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

metabolic syndrome

metabolic syndrome

Intervention Type OTHER

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* aged ≥60 years;
* ASAⅡor Ⅲ
* 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
Minimum Eligible Age

60 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

General Hospital of Ningxia Medical University

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Responsibility Role SPONSOR

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

NZ1651

Identifier Type: -

Identifier Source: org_study_id