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Reduction of allogenic blood transfusion and increased activation of coagulation by re-infusion of post-operative autologous wound blood in patients undergoing total knee and total hip replacement

A randomized controlled double-blind observational trial of re-infusion of post-operative, autologous wound blood in patients undergoing total knee or hip arthroplasty: efficacy (reduction of allogenic blood transfusion) and activation of coagulation (increased coagulation activation in comparison to control group)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN55488814
Enrollment
130
Registered
2012-03-12
Start date
2004-05-12
Completion date
Unknown
Last updated
2016-10-17

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

Conditions

Degenerative arthritis in hip or knee Musculoskeletal Diseases Coxarthrosis, gonarthrosis

Interventions

Pre and at various post operative timepoints blood samples are taken for analysis of several haematological and coagulation parameters [e.g. haemoglobin (Hb), leucocytes, prothrombin time (PT), activa

Sponsors

Maxima Medical Centre (Netherlands)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients aged 18 years or older 2. An indication exists for total knee or hip replacement

Exclusion criteria

Exclusion criteria: 1. Who were using coumarin derivates or heparin 2. Suffering from malignancies or with a history of malignancy within the previous 5 years 3. With a history of venous thromboembolic disease 4. Indicated for revision surgery 5. With less than 100ml collected autologous wound blood

Design outcomes

Primary

MeasureTime frame
1. Hb, APTT, PT, Fibrinogen, TAT, PF 1 + 2 and d-dimer are measured in blood samples taken 12 hours pre operatively and at 3 hours postoperatively and 1 and 4 hours after re-infusion of autologous wound blood and at 24 hours, 14 days, 6 weeks and 3 months post operatively. 2. The number of allogenic blood tranfusions is registred. Allogenic bloodtransfusion is given according to a strictly handled tranfusion protocol 3. Two weeks post operatively a colour duplex sonography is performed

Secondary

MeasureTime frame
1. Number of post-operative transfusion reactions 2. Number of secondary wound infections

Countries

Netherlands

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026