Preterm Parturation

1

Review clinical trials related to Preterm Parturation. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Preterm Parturation Study

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).

Participants needed: 300
Trial details
Age: 18+Biological sex: FemaleType: ObservationalSponsor: Medical University of GrazUpdated: Oct 9, 2026Locations: 1
Eligibility criteria

Preterm rupture of membranes between 20+0 and 36+6 weeks of gestation [+3]

Palliative care plan (neonatal "comfort care") [+5]