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Collection of Autologous Blood Products by Double Erythrocytapheresis

S

Sanquin Research & Blood Bank Divisions

Status and phase

Completed
Phase 3

Conditions

Pre Operative Autologous Donation

Treatments

Procedure: whole blood collection
Procedure: eythrocytapheresis

Study type

Interventional

Funder types

Other

Identifiers

NCT00202475
PPO-C-02-15

Details and patient eligibility

About

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.

Full 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.

Enrollment

100 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Elective surgery

Exclusion criteria

  • Malignancies
  • Severe arrhythmias
  • Congestive heart failure
  • Recent angina
  • Epileptic seizures in the last 3 months before collection

Trial design

Primary purpose

Treatment

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

100 participants in 2 patient groups

1
Active Comparator group
Treatment:
Procedure: eythrocytapheresis
2
Active Comparator group
Treatment:
Procedure: whole blood collection

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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