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
| Type | Name | Description |
|---|---|---|
| DEVICE | Masimo Rainbow Sensor | Non-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.