跳至主要内容
临床试验/NCT06664320
NCT06664320尚未招募不适用

Impact of Mild Acute Normovolemic Hemodilution on Pre-bypass Coagulation Function During Cardiac Surgery

Konkuk University Medical Center1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年10月28日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
状态
尚未招募
入组人数
70
试验地点
1
主要终点
Maximal clot firmness of EXTEM

研究概览

简要总结

The impact of acute normovolemic hemodilution (ANH) using hydroxyethyl starch before initiating cardiopulmonary bypass (CPB) on whole blood viscoelastic profile after CPB has not been well established. Patients undergoing cardiac surgery employing moderate hypothermic CPB are randomly allocated into one of two groups: in Group-ANH, ANH is applied by using a balanced hydroxyethyl starch (HES 130/0.6); and in Group-C, ANH is not applied. After weaning from CPB, intergroup differences of INTEM, EXTEM, FIBTEM, and APTEM profiles are analyzed. As a primary outcome, the inter-group differences between maximal clot firmness of EXTEM will be determined at 10 min after ANH in Group-ANH and that at control.

详细描述

Background: The impact of acute normovolemic hemodilution (ANH) using hydroxyethyl starch before initiating cardiopulmonary bypass (CPB) on whole blood viscoelastic profile after CPB has not been well established. Method: Patients undergoing cardiac surgery employing moderate hypothermic CPB are randomly allocated into one of two groups: in Group-ANH(n=29), ANH is applied by using a balanced hydroxyethyl starch (HES 130/0.6); and in Group-C ANH (n=29)is not applied. Intergroup differences of INTEM, EXTEM, FIBTEM, and APTEM profiles are analyzed. after anesthesia induction (control) and after weaning from CPB and protamine neutralization (after-CPB) in both groups. In Group-ANH, those are determined after ANH (after-ANH). As a primary outcome, the inter-group difference between maximal clot firmness of EXTEM is determined at 10 min after ANH in Group-ANH and that at control. As secondary outcomes, intergroup differences of Hematocrit (Hct), Na+, K+, HCO3-, Ca2+, osmolarity, and s-Cr are determined Intergroup differences of data at T2 are performed.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Outcomes Assessor)

入排标准

年龄范围
19 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients undergoing cardiac surgery with cardiopulmonary bypass who signed written informed consent

排除标准

  • preoperative renal failure requiring reran replacement therapy
  • preoperative liver disease
  • preoperative low cardiac output (EF < 50%)
  • Preoperative IABP application, Atrial fibrillation, Pacemaker
  • contraindication for applying TEE
  • intraoperative withdrawal

研究组 & 干预措施

Acute normovolemic hemodilution group

Active Comparator

patients undergoing cardiac surgery supposed to get aucte normovolemic hemodilution (ANH) before CPB

干预措施: Acute normovolemic hemodilution (ANH) (Procedure)

Acute normovolemic hemodilution group

Active Comparator

patients undergoing cardiac surgery supposed to get aucte normovolemic hemodilution (ANH) before CPB

干预措施: hydroxyethyl starch (HES 130/0.6) (Drug)

结局指标

主要结局

Maximal clot firmness of EXTEM

时间窗: 10 min after completion of acute normovolemic hemodilution (ANH)

Maxiaml clot firmess (MCF) of EXTEM of rotational thromboleastometry

次要结局

  • Clot formation time of EXTEM(10 min after completion of acute normovolemic hemodilution)
  • A10 of FIBTEM(10 min after completion of acute normovolemic hemodilution)

研究者

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

Tae-Yop Kim, MD PhD

Professor of Anesthesiology

Konkuk University Medical Center

研究点 (1)

Loading locations...

相似试验

Mild ANH on Pre-bypass Coagulation Function During... | 临床试验