Skip to content

Safety Assessment of Vaginal Blood Autotransfusion in Cesarean Sections

Safety Assessment of Vaginal Blood Autotransfusion in Cesarean Sections

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2500101750
Enrollment
Unknown
Registered
2025-04-29
Start date
2025-01-22
Completion date
Unknown
Last updated
2025-05-05

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

Conditions

None

Interventions

Control group:None
Experimental group:None

Sponsors

Guangzhou Women and Children's Medical Center
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 1.Pregnant women aged 18 years or older, classified as American Society of Anesthesiologists (ASA) grade II-III. 2.Undergoing planned cesarean section with an expected high risk of hemorrhage and vaginal blood loss >100 mL (meeting at least one of the following criteria: complete placenta previa, placenta accreta, history of postpartum hemorrhage, twin pregnancy). 3.Willing to participate in the study and sign an informed consent form.

Exclusion criteria

Exclusion criteria: 1.Patients or their families refuse to participate in the study. 2.Technical contraindications (e.g., severe hemolysis). 3.Rh-negative patients or those with blood disorders, autoimmune diseases, acute fatty liver of pregnancy (AFLP), or HELLP syndrome. 4.Patients who received anticoagulation therapy preoperatively, underwent allogeneic blood transfusion within the past three months, participated in other clinical studies during pregnancy, or are unable to undergo vaginal blood salvage. 5.Presence of conditions that may hinder study participation, such as psychiatric disorders or language comprehension difficulties. 6.Patients with sickle cell anemia.

Design outcomes

Primary

MeasureTime frame
The positive rate of microbial culture of vaginal blood and peritoneal blood after washing and filtration;

Secondary

MeasureTime frame
The distribution of microbial species in the filtered vaginal blood after recycling;The distribution of microbial species in the filtered peritoneal blood after recycling;The positive rate of microbial culture of vaginal secretions after disinfection;The distribution of microbial species in peripheral blood;Amount of vaginal bleeding;Changes in white blood cell count and neutrophil count before and after the operation;Antibiotics used: The duration, types and concentrations of antibiotics used before and after the operation.;The distribution of microbial species in peripheral blood;

Countries

China

Contacts

Public ContactTian Hang

The Affiliated Women and Children’s Hospital of Guangzhou Medical University

tianhang2544@126.com+86 189 0226 8146

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026