Postoperative Quality Recovery Scale (PQRS)

Sponsor
Franco Carli (Other)
Overall Status
Completed
CT.gov ID
NCT01902147
Collaborator
(none)
200
1
21
9.5

Study Details

Study Description

Brief Summary

Recovery following general anesthesia and surgery is a complex issue confounded by the type of surgery, surgical care, inflammation, different anesthetic drugs and techniques, patient co-morbidities, and differing patient and clinician perceptions of what constitutes good recovery. In this observational study, quality of recovery and patient satisfaction will be measured using the Postoperative Quality Recovery Scale (PQRS). This tool includes six domains of recovery: physiological, nociceptive (pain and nausea), emotive (anxiety and depression), functional recovery (return of activities of daily living), self-assessed recovery, and cognitive recovery.

Condition or Disease Intervention/Treatment Phase
  • Other: Postoperative Quality Recovery Scale (PQRS)

Study Design

Study Type:
Observational
Anticipated Enrollment :
200 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
Measuring Recovery in Patients Undergoing Major Abdominal, Thoracic, and Arthroplasty Surgery Using an Enhanced Recovery Program.
Study Start Date :
Nov 1, 2013
Actual Primary Completion Date :
Aug 1, 2015
Actual Study Completion Date :
Aug 1, 2015

Arms and Interventions

Arm Intervention/Treatment
Elective major abdominal, thoracic, and arthroplasty surgery

All consenting patients scheduled for elective major abdominal, thoracic, and arthroplasty surgery will be followed for 8 weeks after surgery to measure the quality of recovering using the PQRS.

Other: Postoperative Quality Recovery Scale (PQRS)
The PQRS is completed prior to surgery to provide baseline values, and then repeated at different intervals: 15 minutes, 40 minutes, 1 and 3 days, and 4-8 weeks after the completion of surgery. Recovery is broadly defined as return to baseline or better.

Outcome Measures

Primary Outcome Measures

  1. Incidence of recovery (return to baseline or better) in the cognitive domain of the PQRS [postoperative day 3]

Eligibility Criteria

Criteria

Ages Eligible for Study:
N/A and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • elective major abdominal, thoracic, and arthroplasty surgery
Exclusion Criteria:
  • Poor comprehension of English or French

Contacts and Locations

Locations

Site City State Country Postal Code
1 Montreal General Hospital Montreal Quebec Canada H3G 1A4

Sponsors and Collaborators

  • Franco Carli

Investigators

  • Principal Investigator: Franco Carli, MD, McGill University Health Centre/Research Institute of the McGill University Health Centre

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Franco Carli, Professor, Department of Anesthesia, McGill University Health Centre/Research Institute of the McGill University Health Centre
ClinicalTrials.gov Identifier:
NCT01902147
Other Study ID Numbers:
  • 13-141-SDR
First Posted:
Jul 18, 2013
Last Update Posted:
Sep 23, 2015
Last Verified:
Sep 1, 2015
Keywords provided by Franco Carli, Professor, Department of Anesthesia, McGill University Health Centre/Research Institute of the McGill University Health Centre

Study Results

No Results Posted as of Sep 23, 2015