Status:
WITHDRAWN
Non-invasive Cardiac Output Monitoring in Obstetric Patients
Lead Sponsor:
Massachusetts General Hospital
Conditions:
Complications; Cesarean Section
Anesthesia; Adverse Effect, Spinal and Epidural
Eligibility:
FEMALE
18-45 years
Phase:
PHASE4
Brief Summary
The investigators hypothesize that continuously measuring stroke volume (SV) and cardiac output (CO) will 1) reveal hemodynamic instability in a timely manner and alert the physician promptly, 2) prov...
Eligibility Criteria
Inclusion
- age 18-45;
- receiving spinal anesthesia or combined spinal and epidural anesthesia to undergo cesarean section
Exclusion
- Patients who have major cardiovascular disease,preexisting of hypertension or gestational hypertension, preeclampsia and body mass index greater than 35kg/m2;
- Patients who have skin lesion at the place where the electrode is supposed to be applied;
- Emergency cesarean section patients.
Key Trial Info
Start Date :
October 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2012
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01516697
Start Date
October 1 2011
End Date
September 1 2012
Last Update
January 18 2017
Active Locations (1)
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1
Massachusetts General Hospital
Boston, Massachusetts, United States, 02114