Continuous Non-Invasive Measurement of Hemoglobin During Parturition

Completed · Not applicable

Conditions studied: Hemorrhage, Cesarean Section

In brief

A non-invasive hemoglobin monitor will be used during cesarean delivery and the values obtained will be compared to values obtained from traditional blood draw.

Key facts

Study ID

NCT03150043

Run by

The University of Texas Medical Branch, Galveston

People needed

65

Starts

2017-05-10

Expected to finish

2018-05-09

Last updated by the study team

2021-02-24

Who can join

Age: 18 and older, up to 50. Sex: female. Healthy volunteers: accepted.

You may qualify if…

• Pregnant women undergoing primary cesarean delivery after failed induction of labor, or repeat cesarean delivery after failed TOLAC (trial of labor after cesarean)
• Pregnant women between the ages of 18-50

You may not qualify if…

• Patient who are not pregnant
• Patients unwilling or unable to provide consent
• Patients under the age of 18
• Patients who are incarcerated

Where it is running

• University of Texas Medical Branch — Galveston, Texas, United States

Full record on ClinicalTrials.gov

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