About this trial

The prevention of perioperative anemia has the potential to reduce complications, hospital stays, and long-term prognosis in patients undergoing bone tumor surgery. Data from previous studies suggest that the clinical efficacy of acute normovolemic hemodilution (ANH) has always been controversial, and intraoperative fluid administration strategy is an important confounding factor. The HEAL trial will assess whether ANH will improve postoperative hemoglobin levels when applying goal-directed fluid therapy in patients undergoing bone tumor surgery.

Eligibility criteria

Qualifiers

age 18 to 75 years;

undergoing elective bone tumor resection surgery;

preoperative hemoglobin ≥11 g/dL;

Disqualifiers

using a tourniquet;

palliative operation or minimally invasive surgery;

BMI<18.5 or >30Kg/m²;

international normalized ratio (INR) >1.5 or platelet count <100 × 10^9/L;

Trial design

Treatments tested in this trial

  • acute normovolemic hemodilution

Treatment groups

32 Participants
are divided into 2 treatment groups

Locations

1
The Second Affiliated Hospital of Zhejiang University anesthesiology department310000, HangzhouZhejiang, China

Sponsors and collaborators

Second Affiliated Hospital, School of Medicine, Zhejiang University

Lead sponsor