Clinical Trials Directory

Trials / Terminated

TerminatedNCT04525534

Plasma Concentration of Biological Markers in Placenta Accreta Spectrum

Plasma Concentration of Biological Markers in Placenta Spectrum

Status
Terminated
Phase
Study type
Observational
Enrollment
19 (actual)
Sponsor
University of Arkansas · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

The purpose of this exploratory study is to determine how well maternal serum biomarkers and placental micro-particles (MP) correlate with placenta accreta spectrum (PAS) at the time of cesarean delivery in women with suspected PAS compared to women without PAS. Our aim is to determine if women with PAS have a unique MP and protein signature at the time of delivery compared with women without PAS.

Detailed description

Maternal blood samples will be taken at various points during the intrapartum period. A healthy group of women admitted for delivery will act as a matched control and will have their blood sampled at similar time points. The primary outcome variables will include the total number of micro-particles, the number of micro-particles from each cell line (platelet, placental, endothelial etc.), and protein markers The knowledge gained from this study has the potential to develop a diagnostic test for PAS with the ability to improve management and outcomes for mother and baby through earlier diagnosis.

Conditions

Interventions

TypeNameDescription
OTHERThere is no other intervention, only clinical treatment.There is no other intervention, only clinical treatment

Timeline

Start date
2020-08-30
Primary completion
2023-07-10
Completion
2023-07-10
First posted
2020-08-25
Last updated
2024-09-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT04525534. Inclusion in this directory is not an endorsement.