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Post Operative Cognitive Dysfunction After Breast Surgery

NCT03774420 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 200

Last updated 2026-04-21

No results posted yet for this 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).

Conditions

  • Emergence Delirium
  • Post-Operative Cognitive Dysfunction

Sponsors & Collaborators

  • University of Padova

    lead OTHER

Principal Investigators

  • Federico Linassi, MD · University of Padova

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2019-07-03
Primary Completion
2027-11-30
Completion
2027-12-31

Countries

  • Italy

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03774420 on ClinicalTrials.gov