Systemic Inflammation Versus Acute Pain in Total Knee Arthroplasty (TKA)
NCT ID: NCT01322074
Last Updated: 2011-10-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
120 participants
OBSERVATIONAL
2009-08-31
2011-10-31
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Level of systemic inflammatory markers (CRP and IL6) are measured preoperatively and 4 and 24 hours postoperatively. These measurements are correlated to postoperative pain (a detailed assessment of pain at rest and during ambulation).
We pole blood-samples collected prospectively (from two data set)
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Total knee arthroplasty
Patients operated with elective, unilateral total knee arthroplasty.
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Able to speak and understand danish
* Able to give informed consent
Exclusion Criteria
* Allergies to local anesthetics or methylprednisolone
* Age \< 18 years old
* Daily use of strong opioids or glucocorticoids
* Pregnancy or breastfeeding (fertile women)
* Bilateral / revision arthroplasty
* Dementia or other cognitive dysfunction
* Diabetic neuropathy, rheumatoid arthritis, and neurologic or psychiatric diseases potentially influencing pain perception
18 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Hvidovre University Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Troels Haxholdt Lunn
MD
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Dep. of Anesthsiology, Hvidovre University Hospital
Copenhagen, Hvidovre, Denmark
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
9991999
Identifier Type: -
Identifier Source: org_study_id