Skip to main content
Clinical Trials/NCT05341362
NCT05341362
Recruiting
Not Applicable

Hemodynamic Management Target on Continuous Monitoring in Cesarean Delivery-A Randomized Controlled Trial in Patients With Supine Hypotensive Syndrome

China Medical University, China1 site in 1 country60 target enrollmentApril 17, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Supine Hypotensive Syndrome
Sponsor
China Medical University, China
Enrollment
60
Locations
1
Primary Endpoint
Umbilical arterial blood gas PH
Status
Recruiting
Last Updated
3 years ago

Overview

Brief Summary

Supine hypotensive syndrome often occurs following spinal anesthesia for cesarean delivery.In our study we base the regulation and drug administration both on the regular monitor and on a novel monitor which reflects upon the hemodynamic changes. Our aim is to observe whether the outcome of SHS patients with anesthesia management based on hemodynamic figures differs from those based on experience.

Registry
clinicaltrials.gov
Start Date
April 17, 2022
End Date
June 1, 2023
Last Updated
3 years ago
Study Type
Interventional
Study Design
Parallel
Sex
Female

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Yuqing Li

Undergraduate doctor

China Medical University, China

Eligibility Criteria

Inclusion Criteria

  • American Society of Anesthesiologists (ASA) Physical Status Classification II and had no significant cardiovascular, pulmonary, renal or endocrine disease, without contraindications to CSEA,and could be diagnosed as SHS according to the criteria.

Exclusion Criteria

  • Patients undergoing emergency CD, CD under general anesthesia or patients' refusal to participate, or multiple fetations.

Outcomes

Primary Outcomes

Umbilical arterial blood gas PH

Time Frame: 30minutes

The value is tested immediately after the blood sample is achieved after the infant is born.

Secondary Outcomes

  • Umbilical blood gas lactate(30minutes)
  • total vasopressor dosage(30 minutes)
  • Time span(2 hours)
  • Discomfort Score(1day)

Study Sites (1)

Loading locations...

Similar Trials