MCID and PASS for Acute Pain and Quality of Recovery After Orthopedic Surgery

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18-80
SponsorUniversity Health Network, Toronto

About this trial

This study seeks to define what constitutes an MCID and a PASS in patients undergoing a variety of elective major orthopedic surgery.

Eligibility criteria

Qualifiers

Adult patients aged 18-80 years

ASA class I - III

Primary elective surgery

unilateral total hip replacement

Disqualifiers

Inability to give informed consent

Poor English comprehension

Psychiatric disorders e.g., dementia

Known allergies to morphine / hydromorphone

Trial design

Treatments tested in this trial

  • 1.Baseline Measurements Before Surgery
  • 2.Intraoperative Anesthetic Management
  • 3.Postoperative Analgesic Management
  • 4.Postoperative NRS Pain Assessment
  • 5.Postoperative Global Rating Scale (GRS) Pain Assessment
  • 6.Postoperative Patient Acceptable Symptom State (PASS) Assessment for Pain
  • 7.Postoperative Quality of Recovery Assessment
  • 8.Other Postoperative Assessments

Treatment groups

300 Participants
are divided into 1 treatment group