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The Effects of Hemodilution Methods in Patients Undergoing Primary Debulking Gynaecological Surgery

The Effects of Two Hemodilution Methods on Vascular Endothelial Function in Patients Undergoing Primary Debulking Gynaecological Surgery

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06103214
Enrollment
144
Registered
2023-10-26
Start date
2017-01-01
Completion date
2023-01-31
Last updated
2023-10-26

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

Conditions

Ovarian Neoplasm Epithelial

Keywords

Acute normovolemic hemodilution (ANH), Acute hypervolemic hemodilution (AHH), Ovarian cancer

Brief summary

Primary cytoreductive surgery for ovarian cancer is an ideal setting to evaluate endothelial function under ANH and AHH, as the procedure is associated with moderately high blood loss. As the technique has not yet been described in this setting, investigators designed a pilot study to evaluate ANH and AHH in patients planned to undergo primary cytoreduction during perioperative period, with the intent of proceeding to a randomized trial if results were favorable.

Detailed description

Using a computer-generated random number table, patients were randomized to three groups: Control Group(n=30), ANH Group(n=30) and AHH Group(n=30). Patients underwent standard preoperative preparation for cytoreductive surgery according to institutional standards.All patients who underwent a standard anesthesia protocol and similar surgical procedures were considered for the analysis. For this purpose, investigators only included patients who underwent the following interventions: radical hysterectomy, bilateral adnexectomy, one or more bowel resection, peritonectomy, pelvic lymphadenectomy and extended periaortic lymphadenectomy. The patient would be ruled out of the experiment when the participant was accompanied with any kind of serious complications such as wakening delay and drug allergy.

Interventions

Acute normovolemic hemodilution (ANH) is a medical procedure that involves removing a certain volume of blood from a patient before surgery and replacing it with a volume expander or blood substitute. The goal of ANH is to reduce the need for blood transfusions during or after surgery. During the ANH procedure, a patient's blood is typically withdrawn and replaced with a crystalloid or colloid solution. This dilutes the patient's blood, reducing the concentration of red blood cells. The withdrawn blood is then stored and can be reinfused back into the patient after the surgical procedure is completed.

OTHERacute hypervolemic hemodilution (AHH)

The purpose of diluting the blood with fluids and removing some of the red blood cells is to decrease the viscosity of the blood. This can improve blood flow and oxygen delivery to tissues, especially in cases of decreased blood flow or oxygenation.

Sponsors

Zhejiang Cancer Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Clinical diagnosis of advanced primary epithelial ovarian 2. No comorbidities nor functional limitations (ASA Grade II due to high tumor load) 3. Serum hemoglobin (Hb) before surgery ≥ 11g/dl 4. Hematocrit (Hct) ≥ 35% 5. Quantity of platelets ≥ 100 × 109 /L

Exclusion criteria

1. Age \<18 or \>65 years 2. Body mass index \<20 and \>30 kg/m2 3. Duration of surgery \<180 min 4. Severe cardiovascular disease, liver and kidney disease 5. Thromboembolism history

Design outcomes

Primary

MeasureTime frameDescription
Endothelin-1 (ET-1)three periods: before hemodilution, immediate postoperative period, and 24 hours laterBlood sample (5 ml) was obtained from the vein,Endothelin-1 (ET-1) was measured using the enzyme-linked immunosorbent assay (ELISA) (Merck & Co Inc, USA) according to manufacturer's instructions.

Secondary

MeasureTime frameDescription
von Willebrand factor (VWF), tissue factor pathway inhibitor (TFPI), plasminogen activator inhibitor 1 (PAI-1) and thrombomodulin (TM) levelsthree periods: before hemodilution, immediate postoperative period, and 24 hours latervon Willebrand factor (VWF), tissue factor pathway inhibitor (TFPI), plasminogen activator inhibitor 1 (PAI-1) and thrombomodulin (TM) levels were measured using the enzyme-linked immunosorbent assay (ELISA) (Merck & Co Inc, USA) according to manufacturer's instructions.

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026