Postoperative Pain
Conditions
Keywords
postoperative pain treatment
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.
Interventions
DRUGPain treatment
Registration af actual analgesic treatment and outcomes
Sponsors
Zealand University Hospital
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| NRS pain during mobilization | 6 hours postoperatively |
| Total morphine-eqv. opioid consumption | 24 hours postoperatively |
Secondary
| Measure | Time frame |
|---|---|
| Nausea | 6 hours postoperatively |
| Vomiting | Number of episodes during 24 hours postoperatively |
| NRS pain at rest | 6 hours postoperatively |
| Sedation | 6 hours postoperatively |
| Length of hospital stay | Number of days until discharge |
| Dizziness | 6 hours postoperatively |
| NRS pain during mobilization | 24 hours postoperatively |
Countries
Denmark
Outcome results
None listed