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Post Operative Cognitive Dysfunction and Delirium After Spinal Surgery

U

University of Padova

Status

Unknown

Conditions

Emergence Delirium
Post-Operative Cognitive Dysfunction

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Aim of this trial is to define if Post-Operative Cognitive Dysfunction and Delirium, detected analyzing changes between pre-operative and post-operative Neurocognitive Test, relate to concentration of effector's site concentration of propofol and remifentanil TCI and to the common intraoperative neuromonitoring values.

Full description

Post-Operative Cognitive Dysfunction and Emergence Delirium has not been yet investigated after general anaesthesia with Targeted-Controlled-Infusion (TCI), daily used in the investigator's Hospital to anesthetize patients undergoing spinal surgery. Aim of this trial is to define if neurocognitive tests (Pfeiffer test, Montreal Cognitive Assessment, Trail Making Test A and B, Digit Span Test, Confusion Assessment Method) before and after surgery relate to concentrations at effector's site (Ec) of propofol and remifentanil TCI, the values of Bispectral Index, blood pressure values and usage of drugs to increase arterial blood pressure.

Enrollment

200 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • General Anaesthesia delivered with Propofol and Remifentanil with Targeted Controlled Infusion
  • Surgical duration > 60 minutes

Exclusion criteria

  • Neurological pathologies

Trial contacts and locations

0

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Central trial contact

Federico Linassi, MD

Data sourced from clinicaltrials.gov

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