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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 16 December 2017
Main ID:  NCT02340052
Date of registration: 13/01/2015
Prospective Registration: No
Primary sponsor: Zealand University Hospital
Public title: Pain Map DK: a Prospective Cohort Study of Pain Treatment in 500 Hip Arthroplasty Patients at Different Danish Hospitals
Scientific title:
Date of first enrolment: April 2014
Target sample size: 501
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02340052
Study type:  Observational
Study design:   
Phase:  N/A
Countries of recruitment
Denmark
Contacts
Name:     Ole Mathiesen, MD. PhD
Address: 
Telephone:
Email:
Affiliation:  Head of research, department of anaesthesiology, Koege hospital
Key inclusion & exclusion 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



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Postoperative Pain
Intervention(s)
Drug: Pain treatment
Primary Outcome(s)
NRS pain during mobilization [Time Frame: 6 hours postoperatively]
Total morphine-eqv. opioid consumption [Time Frame: 24 hours postoperatively]
Secondary Outcome(s)
Sedation [Time Frame: 24 hours postoperatively]
Sedation [Time Frame: 6 hours postoperatively]
Dizziness [Time Frame: 24 hours postoperatively]
Length of hospital stay [Time Frame: Number of days until discharge]
NRS pain at rest [Time Frame: 24 hours postoperatively]
Nausea [Time Frame: 24 hours postoperatively]
Nausea [Time Frame: 6 hours postoperatively]
Dizziness [Time Frame: 6 hours postoperatively]
NRS pain at rest [Time Frame: 6 hours postoperatively]
NRS pain during mobilization [Time Frame: 24 hours postoperatively]
Vomiting [Time Frame: Number of episodes during 24 hours postoperatively]
Secondary ID(s)
SM1-AG-2014
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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