Non-invasive Point-Of-Care Hemoglobin Testing In An Obstetric Population

Status: Recruiting
Location: See location...
Intervention Type: Device
Study Type: Observational
SUMMARY

Anemia is common during pregnancy due to increased metabolic rate and normal physiologic changes associated with pregnancy. Anemia during pregnancy has been associated with increased of adverse outcomes during delivery and the postpartum period. Currently, it is recommended to screen for anemia at three pre-specified points during routine prenatal care, typically 3 months apart. This screening method may miss patients who develop anemia between these intervals and lead to a delay in diagnosis and treatment. MasimoTM has developed a non-invasive device that can detect anemia without a blood draw. This device has not been extensively studied in pregnant patients. The aim of this study is to determine the agreement in hemoglobin readings between the non-invasive device and the standard of care blood draws in pregnant patients.

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Maximum Age: 60
Healthy Volunteers: f
View:

• Pregnant or postpartum;

• Age ≥18 years old;

• Undergoing phlebotomy for clinical purpose

Locations
United States
Massachusetts
Beth Israel Deaconess Medical Center
RECRUITING
Boston
Time Frame
Start Date: 2024-12-01
Estimated Completion Date: 2026-08
Participants
Target number of participants: 125
Related Therapeutic Areas
Sponsors
Leads: Beth Israel Deaconess Medical Center

This content was sourced from clinicaltrials.gov