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

NCT06254092 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 28

Last updated 2024-02-12

No results posted yet for this study

Summary

This study was conducted to investigate whether the use of tourniquet after delivery of the fetus could reduce the amount of amniotic fluid entering the bloodstream and thus reduce the incidence of intraoperative adverse events.

Conditions

  • Amniotic Fluid Embolism
  • Pulmonary Hypertension

Interventions

PROCEDURE

tourniquet binding of cervical

The procedure will be performed by surgeons with rich experience in clinical work

Sponsors & Collaborators

  • First People's Hospital of Chenzhou

    lead OTHER

Principal Investigators

  • Zhiming zhang · Chenzhou NO. 1 people's Hospital

Study Design

Allocation
NA
Purpose
PREVENTION
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
20 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2024-01-31
Primary Completion
2024-07-01
Completion
2024-08-01

Countries

  • China

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06254092 on ClinicalTrials.gov