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Clinical Trials/NL-OMON35562
NL-OMON35562
Completed
Not Applicable

*The effect of duration of wound drainage on allogeneic blood transfusions using a postoperative retransfusion system after major orthopaedic surgery* - Bellovac ABT drain duration study

Medisch Centrum Haaglanden0 sites570 target enrollmentStarted: TBDLast updated:
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Conditionsblood transfusionosteoarthritits1002321310003184

Overview

Phase
Not Applicable
Status
Completed
Enrollment
570
OverviewEligibility CriteriaInvestigatorsRecords & IdentifiersSimilar Trials

Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 to 99 (—)

Inclusion Criteria

  • •\- Patients scheduled to undergo elective major orthopaedic surgery (hip, knee)
  • •\- Male and non\-pregnant female patients between 18\-80 years of age.
  • •\- Patients who signed the Ethics Committee approved specific Informed Consent Form prior to surgery.

Exclusion Criteria

  • •\- Patients with a major surgical procedure during the 12 weeks before the study\-related operation.
  • •\- No other used alternatives to reduce allogeneic blood transfusions, such as preoperative epoetin alpha (Eprex®) injections or intra\-operative cell saving (Sangvia®).
  • •\- Clinical or laboratory evidence of untreated iron, folate or vitamin B12 deficiency.
  • •\- Recent Myocardial Infarction or CVA (\<3 months).
  • •\- Dutch language not mastered.
  • •\- The patient is pregnant or planning a pregnancy after surgery (or is using inadequate birth control).
  • •\- Mentally disabled patients.
  • •\- Current malignancy or any active infection.

Investigators

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