NCT05341362
Recruiting
Not Applicable
Hemodynamic Management Target on Continuous Monitoring in Cesarean Delivery-A Randomized Controlled Trial in Patients With Supine Hypotensive Syndrome
ConditionsSupine Hypotensive Syndrome
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.
Investigators
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)
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