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Clinical Trials/NCT02340052
NCT02340052
Completed
Not Applicable

Pain Map DK: a Prospective Cohort Study of Pain Treatment in 500 Hip Arthroplasty Patients at Different Danish Hospitals

Zealand University Hospital3 sites in 1 country501 target enrollmentApril 2014

Overview

Phase
Not Applicable
Intervention
Pain treatment
Conditions
Postoperative Pain
Sponsor
Zealand University Hospital
Enrollment
501
Locations
3
Primary Endpoint
Total morphine-eqv. opioid consumption
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

This is a prospective observational cohorte study. The aim is to investigate actual pain treatment and outcomes in a large population of total hip arthroplasty patients at 5 different hospitals in Denmark.

Registry
clinicaltrials.gov
Start Date
April 2014
End Date
June 1, 2016
Last Updated
9 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Anja Geisler

RCCN

Zealand University Hospital

Eligibility Criteria

Inclusion Criteria

  • Primary planned total hip arthroplasty, Able to understand and speak english or danish.

Exclusion Criteria

  • patients not able to cooperate, patients with alcohol or drug abuse

Arms & Interventions

Frederiksberg Hospital

100 patients undergoing planned total hil arthroplasty

Intervention: Pain treatment

Koege hospital

100 patients undergoing planned total hil arthroplasty

Intervention: Pain treatment

Naestved Hospital

100 patients undergoing planned total hil arthroplasty

Intervention: Pain treatment

Hilleroed Hospital

100 patients undergoing planned total hil arthroplasty

Intervention: Pain treatment

Nykoebing Falster Hospital

100 patients undergoing planned total hil arthroplasty

Intervention: Pain treatment

Outcomes

Primary Outcomes

Total morphine-eqv. opioid consumption

Time Frame: 24 hours postoperatively

NRS pain during mobilization

Time Frame: 6 hours postoperatively

Secondary Outcomes

  • Vomiting(Number of episodes during 24 hours postoperatively)
  • Dizziness(24 hours postoperatively)
  • Sedation(24 hours postoperatively)
  • Length of hospital stay(Number of days until discharge)
  • NRS pain at rest(24 hours postoperatively)
  • NRS pain during mobilization(24 hours postoperatively)
  • Nausea(24 hours postoperatively)

Study Sites (3)

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