NCT05341362RecruitingNot 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 enrollmentStarted: April 17, 2022Last updated:
Conditions
Trial Snapshot
- Phase
- Not Applicable
- Status
- Recruiting
- Enrollment
- 60
- Locations
- 1
- Primary Endpoint
- Umbilical arterial blood gas PH
Study 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.
Study Design
- Study Type
- Interventional
- Allocation
- Randomized
- Intervention Model
- Parallel
- Primary Purpose
- Prevention
- Masking
- Double (Investigator, Outcomes Assessor)
Eligibility Criteria
- Ages
- 22 Years to 45 Years (Adult)
- Sex
- Female
- Accepts Healthy Volunteers
- No
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)
Investigators
Yuqing Li
Undergraduate doctor
China Medical University, China
Study Sites (1)
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