Clinical Trials Directory

Trials / Completed

CompletedNCT03409822

Non-invasive Hemoglobin Monitoring in Cesarean Section

The Effectiveness of Intraoperative Non-invasive Hemoglobin Monitoring in Parturients With Placenta Previa Undergoing Cesarean Section: Prospective Observational Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
39 (actual)
Sponsor
Seoul National University Bundang Hospital · Academic / Other
Sex
Female
Age
20 Years – 50 Years
Healthy volunteers
Not accepted

Summary

Non-invasive hemoglobin monitoring will be performed in patients who underwent cesarean section with placenta previa and this will be compared with actual laboratory findings. The investigators will investigate whether noninvasive hemoglobin monitoring can adequately reflect the massive bleeding that occurs within a short period of time and find out if it matches the actual laboratory findings.

Conditions

Interventions

TypeNameDescription
DEVICEMasimo SpHb™ monitorAttach the Masimo Rainbow SET® Radical-7 ™ pulse oximeter probe to the third or fourth finger and perform a Masimo SpHb ™ monitor.

Timeline

Start date
2018-02-05
Primary completion
2018-12-30
Completion
2018-12-30
First posted
2018-01-24
Last updated
2019-01-17

Locations

1 site across 1 country: South Korea

Source: ClinicalTrials.gov record NCT03409822. Inclusion in this directory is not an endorsement.