Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-90
SponsorIRCCS Azienda Ospedaliero-Universitaria di Bologna
About this trial
The primary objective of the study is to describe the value of interhemispheric asymmetry (ASYM), during the different intra- and peri-operative phases, in those patients who develop or do not develop post-operative delirium (POD) during the first 30 post-operative days and postoperative cognitive disfunction (POCD) in the first 90 post-operative days, in a population undergoing head\&neck and plastic surgery with a priori increased probability of POD.
Eligibility criteria
Qualifiers
Age> 70;
Male sex; or ASA III;
Smoker;
High blood pressure;
Disqualifiers
ASA IV, V or ASA IE, IIE, IIIE (patients with anesthetic risk ASA>III and those undergoing urgent-emergency surgery will be excluded from the study);
Stroke;
Dementia;
Cerebral aneurysm;
Trial design
Treatments tested in this trial
- Bilateral Bispetral Index Monitor will be applied on forehead of our patients, before surgery begins
Treatment groups
84 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov