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Non-Invasive Hemoglobin Monitoring of Women Undergoing Cesarean Delivery

Stony Brook University logo

Stony Brook University

Status

Completed

Conditions

Complications of Pregnancy, Childbirth and the Puerperium

Treatments

Device: Masimo Rainbow Sensor

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

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.

Full 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.

Enrollment

50 patients

Sex

Female

Ages

18 to 50 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Women undergoing scheduled cesarean delivery

Exclusion criteria

  • Blood disorders (i.e. thalassemia, sickle cell), hypertensive disorders, obstetric risk factors for hemorrhage

Trial design

50 participants in 1 patient group

Women Undergoing Scheduled Cesarean Delivery
Description:
We will be recruiting women who are scheduled for an elective repeat or primary cesarean delivery.
Treatment:
Device: Masimo Rainbow Sensor

Trial contacts and locations

1

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Central trial contact

Joseph Chappelle, MD

Data sourced from clinicaltrials.gov

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