Clinical Trials Directory

Trials / Not Yet Recruiting

Not Yet RecruitingNCT06473818

Non-invasive vs Invasive Cardiac Output Monitoring During Cesarean Section

Non-invasive vs Invasive Cardiac Output Monitoring in Patients Under Spinal Anesthesia During Cesarean Section: a Prospective Observational Study

Status
Not Yet Recruiting
Phase
Study type
Observational
Enrollment
50 (estimated)
Sponsor
General Hospital of Ningxia Medical University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

This study aims to evaluate the consistency of hemodynamic monitoring between NICAP and NICCO technologies (T20A; Chongqing, China) and the traditional pulse wave analysis method (EV1000; USA).

Detailed description

The uterine placenta lacks autonomous regulatory ability, thus making maternal cardiac output (CO) the primary source of blood supply. Therefore, monitoring hemodynamics, including maternal CO, is of significant importance and provides guidance for anesthesia decisions such as fluid management and the administration of vasopressors during cesarean section. This study aims to evaluate the consistency of hemodynamic monitoring between NICAP and NICCO technologies (T20A; Chongqing, China) and the traditional pulse wave analysis method (EV1000; USA).

Conditions

Interventions

TypeNameDescription
DEVICENon-invasive monitoringNon-invasive cardiac output monitoring
DEVICEInvasive monitoringInvasive cardiac output monitoring

Timeline

Start date
2024-09-01
Primary completion
2024-11-30
Completion
2024-11-30
First posted
2024-06-25
Last updated
2024-06-25

Source: ClinicalTrials.gov record NCT06473818. Inclusion in this directory is not an endorsement.