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Non-invasive vs Invasive Cardiac Output Monitoring During Cesarean Section

NCT06473818 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 45

Last updated 2026-05-01

No results posted yet for this study

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).

Conditions

  • Hemodynamics

Interventions

DEVICE

Non-invasive monitoring

Non-invasive cardiac output monitoring

DEVICE

Invasive monitoring

Invasive cardiac output monitoring

Sponsors & Collaborators

  • General Hospital of Ningxia Medical University

    lead OTHER

Principal Investigators

  • Yi Chen, M.D. · General Hospital of Ningxia Medical University

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-01
Primary Completion
2026-01-21
Completion
2026-01-21

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06473818 on ClinicalTrials.gov