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Clinical Trials in Italy / NCT03774420
Recruiting Observational

Post Operative Cognitive Dysfunction After Breast Surgery

NCT03774420 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2019-07-03
Last updated
2026-04-21

Condition(s) studied

Emergence DeliriumPost-Operative Cognitive Dysfunction

Study summary

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

Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * General Anaesthesia delivered with Propofol and Remifentanil with Targeted Controlled Infusion * Use of Laryngeal Mask airway Exclusion Criteria: * Neurological pathologies * Haemodynamical instability during surgery

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Treviso Regional Hospital Treviso TV Recruiting

More University of Padova trials in Italy

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03774420 on ClinicalTrials.gov ↗ ← All trials in Italy