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Not yet recruiting NCT06905353

Quality of Recovery in the Post-anesthesia Care Unit

Observational Postoperative Quality of Recovery Postoperative Quality of Recovery in the Postanesthesia Care Unit

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: Postoperative Quality of Recovery, Postoperative Quality of Recovery in the Postanesthesia Care Unit. Basic parameters: from 18 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 →
Official title

Quality of Recovery in the Post-anesthesia Care Unit - Minimal Clinically Important Difference and Correlation with Postoperative Quality of Recovery One Day After Non-cardiac Surgery

Overview

This prospective observational study aims to identify the minimal clinically important difference of the QoR-PACU2 questionnaire. In addition, this study aims to assess the correlation between self-reported quality of postoperative recovery early after surgery in the post-anesthesia care unit and postoperative recovery on the first day after surgery.

Primary outcome measures

  • Minimal clinically important difference of QoR-PACU2 [Time frame: From preoperative assessment to the day of surgery in the post-anesthesia care unit]
  • correlation between quality of recovery at two time points of assessment [Time frame: from the day of surgery to the first postoperative day]

Eligibility criteria

Inclusion criteria

  • elective non-cardiac surgery
  • expected duration of surgery ≥60 minutes
  • postoperative stay at the post-anesthesia care unit

Exclusion criteria

  • surgery or condition requiring postoperative treatment at an intensive care unit
  • inability to give informed consent/requirement of a legal guardian

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: NCT06905353 · 2025-101434-BO-ff

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗