The Efficacy of Hemo-Quic

The Efficacy of Hemo-Quic A Randomized Controlled Trial Comparing Gravity-Based Blood Collection

Status

Recruiting

Phases

Phase 2

Study type

Interventional

Source

JPRN

Registry ID

JPRN-jRCT1032240470

Enrollment

200

Registered

2024-11-07

Start date

2024-12-12

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-cardiac surgery Non-cardiac surgery

Interventions

Comparison of blood collection methods using gravity versus Hemoquick in performing acute normovolemic hemodilution.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: (1)Patients who are 20 years old or older (2)Patients who weigh 50 kg or more (3)Patients whose hemoglobin level is 11 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

Exclusion criteria

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

Design outcomes

Primary

Measure	Time frame
Whether 400 g of blood was collected within 30 minutes	—

Secondary

Measure	Time frame
Time required to collect 400 g of blood, and the dosage of vasopressors used during blood collection	—

Contacts

Public ContactUeda Kenichi

Kameda General Hospital

kameda.anesthe@gmail.com+81-4-7092-2211

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026