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Serum Immunologic Markers Levels in During the Delivery (DIMDOED)

B

Brno University Hospital

Status

Completed

Conditions

Immunologic Markers

Treatments

Diagnostic Test: Blood sampling

Study type

Observational

Funder types

Other

Identifiers

NCT03664999
KDAR FN Brno 2018/9

Details and patient eligibility

About

This study aim to describe dynamics of immunologic markers C1 inhibitor, C3, C4 during the delivery in order to improve early diagnostics of obstetric emergencies, especially with immune etiology.

Full description

Our prospective observational study will explore the differences between dynamics of the complement components C1 inhibitor, C1 inhibitor activity, C3, C4 during the labour in a group of women with physiologic pregnancy and in a group with a risk of complications (pre-eclampsia, HELLP syndrome, placenta praevia, placental abruption, IUGR, previous post partum hypotony).

We will focus on women undergoing the Caesarean delivery. We will also measure D vitamin levels and ACE levels and search for some contexts.

Enrollment

57 patients

Sex

Female

Ages

15 to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Pregnant women undergoing the Caesarean delivery
  • Signed informed consent

Exclusion criteria

  • Previous hepatitis or other hepatocyte damage

Trial design

57 participants in 2 patient groups

Parturients physiologic pregnancy
Description:
Parturients undergoing caesarean delivery with physiologic pregnancy
Treatment:
Diagnostic Test: Blood sampling
Parturients with risk pregnancy
Description:
Parturients undergoing caesarean with risk of complications (pre-eclampsia, HELLP syndrom, placenta praevia, placental abruption, IUGR, previous post partum hypotony).
Treatment:
Diagnostic Test: Blood sampling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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