Post Operative Cognitive Dysfunction After Breast Surgery
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorUniversity of Padova
About this trial
Aim of this trial is to define if Post-Operative Cognitive Dysfunction, detected analyzing changes between pre-operative and post-operative Neurocognitive Test, and Postoperative Delirium, relate to concentration of effector's site concentration of propofol and remifentanil TCI and to the common intraoperative neuromonitoring values as well as to Pupillometry values (in particular Pupil Diameter, Pupil Latency, and Maximum Contraction Velcoity).
Eligibility criteria
Qualifiers
General Anaesthesia delivered with Propofol and Remifentanil with Targeted Controlled Infusion
Use of Laryngeal Mask airway
Disqualifiers
Neurological pathologies
Haemodynamical instability during surgery
Trial design
Treatments tested in this trial
- Not listed
Trial groups
No trial groups listed
Sponsors and collaborators
Source ClinicalTrials.gov