Trials / Completed
CompletedNCT00202475
Collection of Autologous Blood Products by Double Erythrocytapheresis
Collection of Autologous Blood Products by Double Erythrocytapheresis - Cost Effectiveness Study
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 100 (actual)
- Sponsor
- Sanquin Research & Blood Bank Divisions · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The project will determine the advantages of double erythrocytapheresis in the collection of preoperative autologous erythrocytes as compared to the standard collections of whole blood. The study will assess the total reduction in the number of procedures required to obtain the preoperative units ordered by the surgeon. Also, successfulness of erythrocytaphereses versus classical whole blood collection for these patients will be compared.
Detailed description
The project will determine the advantages of double erythrocytapheresis in the collection of preoperative autologous erythrocytes as compared to the standard collections of whole blood. The study will assess the total reduction in the number of procedures required to obtain the preoperative units ordered by the surgeon. Also, successfulness of erythrocytaphereses versus classical whole blood collection for these patients will be compared.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | eythrocytapheresis | machinal collection of erythrocytes |
| PROCEDURE | whole blood collection | collection of whole blood |
Timeline
- Start date
- 2003-09-01
- Primary completion
- 2006-09-01
- Completion
- 2007-12-01
- First posted
- 2005-09-20
- Last updated
- 2009-10-20
Locations
2 sites across 1 country: Netherlands
Source: ClinicalTrials.gov record NCT00202475. Inclusion in this directory is not an endorsement.