Amniotic Fluid Analysis

Status Not yet recruiting

Clinical Trial Summary

This is a prospective study that will aid in ensuring the feasibility of timely and correct aspiration of amniotic fluid by study research team that include the clinical team taking care of the patient during her labor, timely transport and interpretation of specimens. It will also assist in providing information for the computation of necessary statistical measures (e.g. sample size, power analysis, etc.) for the study cohorts that lack the needed data in the medical literature.

Clinical Trial Description

Can amniotic fluid be serially aspirated via an Intrauterine pressure catheter (IUPC) and successfully analyzed in labor? Do abnormal amniotic fluid results collected serially predict which laboring patients will develop an intrapartum infection? Can the results predict infection sooner than the current clinical diagnostic criteria as outlined by the 2015 NICHD guidelines? How do the sensitivity, specificity, positive and negative predictive values compare to the 2015 NICHD diagnostic criteria? ;

Study Design

Related Conditions & MeSH terms

Obstetric Labor Complications

Clinical Trial Details

NCT number	NCT06131684
Study type	Interventional
Source	Oregon Health and Science University
Contact	Women's Health Research Unit Department of Ob/Gyn
Phone	503-494-3666
Email	whru@ohsu.edu
Status	Not yet recruiting
Phase	Early Phase 1
Start date	November 2023
Completion date	June 30, 2024

View Details

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