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临床试验/NCT01994330
NCT01994330已完成4 期

Severe Aortic Stenosis and Acquired Von Willebrand´s Disease: The Impact of Desmopressin in Valve-Replacement Surgery

Pontificia Universidad Catolica de Chile1 个研究点 分布在 1 个国家目标入组 13 人开始时间: 2009年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
13
试验地点
1
主要终点
blood loss

研究概览

简要总结

Acquired Von Willebrand disease (type 2A) has been described in patients with severe aortic stenosis, the association of aortic stenosis and Digestive bleeding due to this phenomena has received the name of Heye´s syndrome.

We propose that administering Desmopressin (DDAVP) in patients scheduled to aortic valve replacement surgery will reduce blood loss and transfusion rate.

this was a pilot study

详细描述

Randomized Controlled trial compared with placebo in a double blind fashion. Subjects with severe aortic stenosis (transvalvular gradient >50 mmHg or valvular area of lass than 1 cm2) scheduled for aortic valve replacement were enrolled.

the day of surgery blood samples were taken in order to confirm diagnosis (factor VIII activity and Protein electrophoresis for Von Willebrand´s multimers) and then 0,3 mcg/k of DDAVP or saline equally labeled as "study drug" were administered en 30 minutes a half hour before incision.

Blood loss, postoperative hematocrit and transfusion requirement were measured, plasma sodium was measured as a safety issue.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

性别
All
接受健康志愿者

入选标准

  • severe aortic stenosis defined as mean transvalvular gradient greater or equal to 40 mmHg ot transvalvular area less than 1 cm2
  • scheduled for aortic valve replacement surgery

排除标准

  • combined surgery (plus coronary artery bypass graft or other valve replacement/plasty)
  • Infective Endocarditis
  • previously known haemostatic disorder
  • previous treatment with oral anticoagulants or IIb-IIIa inhibitors (we did not exclude those on acetyl-salicylic acid)

研究组 & 干预措施

Desmopressin

Experimental

0,3 mcg per kilogram of desmopressin in 100 ml of saline, labeled as "study drug" and administered in 30 minutes a half hour before surgical incision

干预措施: desmopressin (Drug)

placebo

Placebo Comparator

100 of saline labeled as "study drug" administered in 30 minutes a half hour before surgical incision

干预措施: desmopressin (Drug)

结局指标

主要结局

blood loss

时间窗: once patient arrives to post anesthesia care unit (approximately 6 hours after drug administration

Blood loss obtained from fluid balance of surgery plus drain output

次要结局

  • need of transfusion(48 hours post administration)
  • postoperative hematocrit(the morning after surgery (18-24 hours after drug administration))

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

MPoblete

Anesthesiologist

Pontificia Universidad Catolica de Chile

研究点 (1)

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