Clinical Trials Directory

Trials / Completed

CompletedNCT01576263

Autologous Blood Transfusion After Local Infiltration

Autologous Blood Transfusion After Local Infiltration Analgesia With Ropivacaine in Total Knee and Hip Arthroplasty

Status
Completed
Phase
Study type
Observational
Enrollment
52 (actual)
Sponsor
Northern Orthopaedic Division, Denmark · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Total knee and hip arthroplasty for osteoarthritis is performed on still broader indications even in elderly patients with previous or current medical conditions. Especially comorbidity like cardiovascular diseases and conditions with increased risk of bleeding or previous thrombo-embolic events are major challenges. To facilitate safe use of ropivacaine as an analgesic, information on the concentrations levels after autologous blood transfusion following local infiltration analgesia is very crucial. However, very limited data are available. To verify the safety of autologous blood transfusion, ropivacaine concentrations were studied in 52 patients undergoing either total knee arthroplasty or total hip arthroplasty.

Conditions

Interventions

TypeNameDescription
DRUGAutologous blood transfusion with ropivacaineLocal infiltration analgesia with ropivacaine 3 mg/kg, max 200 mg
DRUGAutologous blood transfusion with ropivacaineLocal infiltration analgesia with ropivacaine 3 mg/kg, max 200 mg.

Timeline

Start date
2010-03-01
Primary completion
2010-04-01
Completion
2010-06-01
First posted
2012-04-12
Last updated
2015-04-10

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT01576263. Inclusion in this directory is not an endorsement.