N/A
Completed N=65
Continuous Non-Invasive Measurement of Hemoglobin During Parturition
Source: ClinicalTrials.gov NCT03150043 ↗Enrolled (actual)
65
Serious AEs
0.0%
Results posted
Feb 2021
Primary outcomePrimary: Pearson Correlation Coefficient for Hemoglobin Measurements — 0.6 Correlation Coeficient
Summary
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.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Pearson Correlation Coefficient for Hemoglobin Measurements |
0.6 | — |
| SECONDARY Number of Participants Who Required Blood Transfusion |
65 | — |
Eligibility Criteria
Inclusion Criteria
- 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
Exclusion Criteria
- Patient who are not pregnant
- Patients unwilling or unable to provide consent
- Patients under the age of 18
- Patients who are incarcerated
Data sourced from ClinicalTrials.gov (NCT03150043). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.