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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05693285
Other study ID # UU
Secondary ID
Status Completed
Phase
First received
Last updated
Start date November 14, 2022
Est. completion date December 2, 2022

Study information

Verified date January 2023
Source Uppsala University
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Preterm birth is associated with maternal increased risk of cardiovascular disease later in life. In an observational case- control study, investigators want to evaluate whether women with preterm birth have increased levels of biomarkers for cardiovascular disease, to reveal potential pathophysiological mechanisms in common.


Description:

Women with spontaneous preterm birth in first pregnancy and a group of matched controls with spontaneous birth in normal time where invited to participate in the study. Participants were identified from the Biobank of Pregnant Women in Uppsala. Levels of cardiovascular biomarkers will be analyzed in plasma samples from the pregnancy and at a follow-up visit where investigators also collect information about other cardiovascular risk factors and lipid status.


Recruitment information / eligibility

Status Completed
Enrollment 65
Est. completion date December 2, 2022
Est. primary completion date December 2, 2022
Accepts healthy volunteers No
Gender Female
Age group N/A to 60 Years
Eligibility Inclusion Criteria: - Women identified as cases or controls Exclusion Criteria: - System inflammatory disease - Smoking at the time of the pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Other:
No intervention
No intervention

Locations

Country Name City State
Sweden Department of Medical Sciences, Uppsala University Uppsala

Sponsors (1)

Lead Sponsor Collaborator
Uppsala University

Country where clinical trial is conducted

Sweden, 

Outcome

Type Measure Description Time frame Safety issue
Primary Levels of Factor XII in plasma in women with preterm birth in compared to a control group with delivery in normal time. Levels of Factor XII in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
Primary Levels of complement C5 in women with preterm birth in compared to a control group with delivery in normal time. Levels of complement C5 in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
Primary Levels of apolipoprotein M in women with preterm birth in compared to a control group with delivery in normal time. Levels of apolipoprotein M in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
Primary Levels of fibrinogen in women with preterm birth in compared to a control group with delivery in normal time. Levels of fibrinogen in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
Primary Levels of plasma kallikrein in women with preterm birth in compared to a control group with delivery in normal time. Levels of plasma kallikrein in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
Primary Levels of vitamin D binding protein in women with preterm birth in compared to a control group with delivery in normal time. Levels of vitamin D binding protein in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
Primary Levels of cadherin -5 in women with preterm birth in compared to a control group with delivery in normal time. Levels of cadherin -5 in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
Primary Levels of growth/differentiation Factor-15 (GDF-15) in women with preterm birth in compared to a control group with delivery in normal time. preterm birth compared to a control group with delivery in normal time. Levels of growth/differentiation Factor-15 (GDF-15) in plasma will be analyzed at two times, both in the actual pregnancy and at a follow-up visit where information about cardiovascular risk factors and lipid status is collected. spring 2023
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