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NOT YET RECRUITING
NCT07869160

Preterm Parturation Study

Sponsor: Medical University of Graz

View on ClinicalTrials.gov

Summary

In this study (study group) non-invasively measured fetal parameters in pregnant patients with preterm premature rupture of membranes (PPROM) or preterm parturation (cervical dilation before 37+0 weeks of gestation) will be examined for their association with short-term neonatal outcomes as well as with specific hematological and immunological parameters of the newborn. The control group includes pregnant women who are due to give birth around their due date (between 37+0 and 41+3 weeks of gestation, without premature rupture of membranes or preterm parturation).

Official title: Preterm Parturation (PrePart) Studie

Key Details

Gender

FEMALE

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

300

Start Date

2027-01-01

Completion Date

2031-06

Last Updated

2026-10-09

Healthy Volunteers

No

Interventions

OTHER

Fetal ultrasound

Fetal ultrasound (spleen, liver, thymus, heart)

OTHER

blood draw

maternal

OTHER

blood draw

umbilical cord

OTHER

vaginal swab

maternal

Locations (1)

Medical University of Graz Department of Obstetrics and Gynecology

Graz, Styria, Austria