跳至主要内容
临床试验/NL-OMON35562
NL-OMON35562已完成不适用

*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 个研究点目标入组 570 人开始时间: 待定最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
570

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 至 99(—)

入选标准

  • - 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.

排除标准

  • - 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.

研究者

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