Preterm Birth Clinical Trial
Official title:
Investigation of First Trimester Serum Vasohibin-1, Vasohibin-2, Cardiotrophin-1 and Endocan Concentrations in Predicting Adverse Perinatal Outcomes
Verified date | May 2024 |
Source | Umraniye Education and Research Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Investigation of the relationship between maternal serum vasohibin-1, vasohibin-2, cardiotrophin -1 and endocan concentrations at the 11th and 14th weeks of gestation and adverse perinatal outcomes.
Status | Recruiting |
Enrollment | 88 |
Est. completion date | December 30, 2024 |
Est. primary completion date | November 30, 2024 |
Accepts healthy volunteers | |
Gender | Female |
Age group | 18 Years to 39 Years |
Eligibility | Inclusion Criteria: - Those who had the first-trimester screening test between 11 and 14 weeks of pregnancy and are in the low-risk group - Those with singleton pregnancy - Those who did not conceive pregnancy with assisted reproductive treatment methods - Those who do not have any pregestational diseases - Those who do not have any uterine anomalies Exclusion Criteria: - Smokers - Those who are in the high-risk group with the first trimester screening test - Those with multiple pregnancies - Those who conceive with assisted reproductive treatment methods - Those who had any disease before pregnancy - Those who have any uterine anomalies |
Country | Name | City | State |
---|---|---|---|
Turkey | Ümraniye Egitim ve Arastirma Hastanesi | Istanbul | Ümraniye |
Lead Sponsor | Collaborator |
---|---|
Umraniye Education and Research Hospital |
Turkey,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Usability of serum vasohibin-1, vasohibin-2, cardiotropin-1 and endocan concentrations in predicting adverse perinatal outcomes | Usability of serum vasohibin-1, vasohibin-2, cardiotropin-1 and endocan concentrations in predicting adverse perinatal outcomes | 1 year |
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