Not yet recruiting NCT06905366
Cognitive Function and Postoperative Quality of Recovery
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Perioperative Neurocognitive Disorders, Postoperative Quality of Recovery. Basic parameters: from 65 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Association Between Cognitive Function and Postoperative Quality of Recovery - a Prospective Cohort Study
Overview
This study aims to assess the association between perioperative cognitive function and postoperative quality of recovery.
Primary outcome measures
- QoR-15GE [Time frame: first postoperative day]
Eligibility criteria
Inclusion criteria
- elective non-cardiac surgery
- age ≥65 years
- duration of surgery ≥60 years
Exclusion criteria
- inability to give informed consent
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Cohort
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT06905366 · 2025-101433-BO-ff