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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05207800
Other study ID # SAHoWMU-CR2021-07-207
Secondary ID
Status Not yet recruiting
Phase
First received
Last updated
Start date February 10, 2022
Est. completion date July 31, 2023

Study information

Verified date January 2022
Source Second Affiliated Hospital of Wenzhou Medical University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Objective: The aim of this study was to investigate the predictive value of maternal serum pentraxin 3 (PTX3) and heparin-binding protein (HBP) for chorioamnionitis in preterm premature rupture of membranes (PPROM). Method: This observational prospective cohort study included a total of 180 pregnant women at 24-40 gestational weeks. There were 60 cases of term premature rupture of membranes (TPROM), 60 cases of preterm premature rupture of membranes(PPROM)and 60 cases of healthy women. The concentrations of PTX3 and HBP were measured in maternal blood and amniotic fluid using an enzyme-linked immunosorbent assay (ELISA). Western immunoblotting was used to analyze the expression of PTX3 and HBP in placental tissue. The localization and immunoreaction of PTX3 and HBP in placenta were determined via immunohistochemistry (IHC).


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 180
Est. completion date July 31, 2023
Est. primary completion date December 31, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Female
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria: 1. The pregnant woman is born at a gestational age of 24-40 weeks; 2. The pregnant woman has a single child; 3. Regular obstetric examination during pregnancy with complete obstetric examination data was diagnosed as premature rupture of membranes (PROM). Exclusion Criteria: 1. Pregnancy complicated with medical and surgical diseases, such as thyroid dysfunction and chronic hypertension; 2. Insufficiency of vital organ function or complicated tumor; 3. Pregnant women with other pregnancy complications besides PROM, such as preeclampsia, etc.; 4. Neonates had major congenital malformations (congenital anal atresia, congenital biliary atresia, congenital heart disease and so on, whether prenatal suspicion or diagnosis postpartum) 5. Neonatal septicemia, hemolytic disease or other diseases affecting bilirubin metabolism.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
The concentrations of PTX3 and HBP were monitored in maternal blood, placental tissue and amniotic fluid.
The concentrations of PTX3 and HBP were monitored in maternal blood, placental tissue and amniotic fluid.

Locations

Country Name City State
n/a

Sponsors (1)

Lead Sponsor Collaborator
Second Affiliated Hospital of Wenzhou Medical University

Outcome

Type Measure Description Time frame Safety issue
Other PTX3 and HBP concentrations in amniotic fluid PTX3 and HBP concentrations in amniotic fluid 24 weeks to 40 weeks gestation
Primary PTX3 and HBP concentrations in maternal blood PTX3 and HBP concentrations in maternal blood 24 weeks to 40 weeks gestation
Secondary PTX3 and HBP concentrations in placental tissue PTX3 and HBP concentrations in placental tissue 24 weeks to 40 weeks gestation
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