The Efficacy of Hemo-Quic

JRCT ID: jRCT1032240470

Registered date:07/11/2024

Basic Information

• Recruitment status: Pending
• Health condition(s) or Problem(s) studied: Non-cardiac surgery
• Date of first enrollment: 07/11/2024
• Target sample size: 200
• Study type: Interventional
• Intervention(s): Comparison of blood collection methods using gravity versus Hemoquick in performing acute normovolemic hemodilution.

Outcome(s)

• Primary Outcome: Whether 400 g of blood was collected within 30 minutes
• Secondary Outcome: Time required to collect 400 g of blood, and the dosage of vasopressors used during blood collection

Key inclusion & exclusion criteria

• Age minimum: >= 18age old
• Age maximum: Not applicable
• Gender: Both

Include criteria

(1)Patients who are 20 years old or older
(2)Patients who weigh 50 kg or more
(3)Patients whose hemoglobin level is 12 g/dL or higher in preoperative blood tests
(4)Patients scheduled for hemodilutional autologous blood transfusion in non-cardiovascular surgery
(5)Patients who can provide written consent to participate in this study

Exclude criteria

(1)Patients who are pregnant, breastfeeding, or may be pregnant.
(2)Patients whom the attending physician deems unsuitable for participation in this study.

Related Information

• Primary Sponsor: Ueda Kenichi