Clinical Trials Directory

Trials / Completed

CompletedNCT02275507

Non-Invasive Hemoglobin Monitoring of Women Undergoing Cesarean Delivery

Status
Completed
Phase
Study type
Observational
Enrollment
50 (actual)
Sponsor
Stony Brook University · Academic / Other
Sex
Female
Age
18 Years – 50 Years
Healthy volunteers
Accepted

Summary

The purpose of this study is to determine the normal hemoglobin curve during cesarean delivery and for the first 24 hours after surgery to aid in the creation of an algorithm to detect life-threatening bleeding earlier.

Detailed description

Acute and life threatening blood loss is the most common cause of morbidity and mortality for pregnancy women in the US. To date, the only means we have of monitoring the amount of blood loss during a delivery is by the physician estimating the amount. This has been shown to not be very accurate and leads to confusion on when and how much a women should be transfused during a hemorrhage. New devices have been developed over the last few years to monitor blood levels in a accurate and non-invasive fashion. We aim here to use a non-invasive blood monitoring system to evaluate normal blood loss in women undergoing scheduled cesarean delivery. We hope that this will allow us to create a baseline that can be used in subsequent studies to identify women who are losing more blood than normal so that we may intervene faster and avoid unnecessary morbidity.

Conditions

Interventions

TypeNameDescription
DEVICEMasimo Rainbow SensorNon-Invasive Hemoglobin Measurement

Timeline

Start date
2014-10-15
Primary completion
2016-10-30
Completion
2016-10-30
First posted
2014-10-27
Last updated
2024-12-04

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT02275507. Inclusion in this directory is not an endorsement.