Clinical Trials Directory

Trials / Completed

CompletedNCT02698982

Optimized Anesthesia to Reduce Postoperative Cognitive Impairment in the Elderly

Impact of Tight Intraoperative Blood Pressure and Depth of Anesthesia Control on the Incidence of Postoperative Cognitive Impairment in Elderly Patients

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
41 (actual)
Sponsor
Erasme University Hospital · Academic / Other
Sex
All
Age
70 Years
Healthy volunteers
Accepted

Summary

The aim of this study is to demonstrate that in elderly and frail patients, a narrower control of intraoperative blood pressure (BP) by the use of a continuous and noninvasive BP monitoring, coupled with an adequate depth of anesthesia, will reduce the incidence of postoperative cognitive impairment and the hospital length of stay.

Detailed description

Postoperative cognitive impairment (delirium and cognitive dysfunction) are frequent and feared complications in the elderly; they increase the postoperative morbidity and mortality, worsen the cognitive and functional outcome with loss of independence and increase the hospitalization length and costs . However, the etiology of these postoperative cognitive impairment, although probably multifactorial, remains unclear and strongly debated. The investigators hypothesize that excessive anesthesia depths associated with intraoperative hypotension may play a critical role in the pathogenesis of cognitive impairment following surgery.

Conditions

Interventions

TypeNameDescription
DEVICEDepth of anesthesia monitoring (BIS, Covidien USA) and Continus non invasive blood pressure monitoring (Clearsight, Edwards LifeScience, USA)
PROCEDUREmoderate risk surgery

Timeline

Start date
2016-05-01
Primary completion
2017-03-01
Completion
2017-03-01
First posted
2016-03-04
Last updated
2017-12-26

Locations

1 site across 1 country: Belgium

Source: ClinicalTrials.gov record NCT02698982. Inclusion in this directory is not an endorsement.