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NCT03175042

Non-invasive Spot Hemoglobin Measurement in the Outpatient Obstetric Clinic

Completed Last updated 3 June 2019
What this trial tests

trial testing Masimo spot hemoglobin non-invasive monitor in Anemia in Pregnancy in 40 participants. Completed in 31 December 2017.

Timeline
13 June 2017
Primary endpoint
31 December 2017
31 December 2017

Quick facts

Lead sponsorThe University of Texas Medical Branch, Galveston
StatusCompleted
Study typeOBSERVATIONAL
Enrollment40
Start date13 June 2017
Primary completion31 December 2017
Estimated completion31 December 2017
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

The University of Texas Medical Branch, Galveston

Who can join

Adults 18 to 50, female only, with Anemia in Pregnancy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Pregnant patients in the UT Medical Branch outpatient obstetric clinic are screened for anemia via blood draw at first prenatal visit. Those who meet Center for Disease Control (CDC) criteria for anemia during pregnancy (hemoglobin less than 11g/dL in first and third trimesters and hemoglobin less than 10.5g/dL during the second trimester), will be approached for participation in this study. It is the protocol of the UT Medical Branch outpatient obstetric clinic to repeat a blood draw every 4 weeks in patients with anemia. At the time of their blood draw, patients who participate in our study will have the Masimo Spot Non-invasive Hemoglobin monitor placed on our finger. The primary aim of the study is to see how accurate the non-invasive monitor is compared with blood draw. With the potential benefit being earlier diagnosis of anemia and easier method to ensure improvement in the hemoglobin.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03175042.

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