Effect of Tourniquet Binding of Cervical on the Blood Volume of Amniotic Fluid in Cesarean Section

Launched by FIRST PEOPLE'S HOSPITAL OF CHENZHOU · Feb 8, 2024

Keywords

ClinConnect Summary

This clinical trial is looking at a technique called tourniquet binding, which is applied to the neck area after a baby is delivered during a cesarean section. Researchers want to see if this method can help reduce the amount of amniotic fluid that enters the mother's bloodstream. This is important because too much amniotic fluid in the bloodstream can lead to complications during surgery, such as amniotic fluid embolism and pulmonary hypertension.

To participate in this study, women must be pregnant with only one baby and in good health, meaning they should not have high blood pressure or heart disease. They also need to have no conditions that would complicate surgery, such as certain problems with the placenta or previous abdominal surgeries. Participants will need to provide consent, meaning they understand the study and agree to take part. The study is currently not recruiting participants yet, but it's designed to help improve safety for women undergoing cesarean sections.

Gender

FEMALE

Eligibility criteria

• • Inclusion criteria
• • 1. Single pregnancy
• • 2. Be in good health, with no high blood pressure or heart disease during pregnancy
• • 3. Without placenta previa and placenta implantation
• • 4. No abdominal adhesions, suitable for operation
• • 5. Signed informed consent by the pregnant woman and her family
• • Exclusion criteria
• • 1. Serious coagulation abnormality
• • 2. Preoperative severe cardiac, cerebral, pulmonary, hepatic, renal and other important organs insufficiency and electrolyte abnormality combined with placenta praevia or placenta implantation
• • 3. Multiple pregnancies
• • 4. Previous history of abdominal surgery
• • 5. Intraoperative drug allergy