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Autologous Blood Transfusion After Local Infiltration

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

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01576263
Enrollment
52
Registered
2012-04-12
Start date
2010-03-31
Completion date
2010-06-30
Last updated
2015-04-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Total Hip Arthroplasty, Total Knee Arthroplasty

Keywords

Anaesthesia, Infiltration, Blood transfusion, Autologous, Arthroplasty, Replacement, Ropivacaine

Brief 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.

Interventions

DRUGAutologous blood transfusion with ropivacaine

Local infiltration analgesia with ropivacaine 3 mg/kg, max 200 mg

Sponsors

Northern Orthopaedic Division, Denmark
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Clinical diagnosis for hip arthroplasty * Clinical diagnosis for knee arthroplasty

Exclusion criteria

* Patients \< 18 years * Lack of informed consent * Inability to read/understand Danish * Bilateral diagnosis * Cancer diagnosis

Design outcomes

Primary

MeasureTime frameDescription
Concentrations of ropivacaine in serum6 hoursConcentrations of ropivacaine in serum before and after autologous blood transfusion will be analyzed.

Secondary

MeasureTime frameDescription
Analysis of ECG and pulse rate6 hoursECG, pulse rate and blood pressure will be analyzed in proportion to concentrations of serum before and after autologous blood transfusion

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026