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Characteristics of Primary and Plasmatic Hemostasis in Preeclampsia

Characteristics of Primary and Plasmatic Hemostasis in Preeclampsia - a Cross-sectional Study

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03149250
Enrollment
60
Registered
2017-05-11
Start date
2017-09-01
Completion date
2018-02-01
Last updated
2017-08-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Coagulation Disorder, Blood, Platelet Function

Keywords

Aggregometry

Brief summary

The study aims to investigate the impact of preeclampsia on hemostasis.

Detailed description

In comparison to healthy pregnant women and non-pregnant woman, this study analyses parameters of primary hemostasis and plasmatic coaguation in preeclamptic pregnant woman. Detailed analyses of the platelet function is performed using the Multiple Electrode Aggregometry, detailed analyses of the plasmatic coagulation syste is performed by isolated coaguation factor analyses and conventional coagulation analyses.

Interventions

DIAGNOSTIC_TESTAggregometry, Monitoring of plasmatic hemostasis

Multiple Electrode Aggregometry using the Multiplate system Coagulation factor analyses (FXIII, FVIII, vWF) Parameters of conventional coagulation testing (aPTT, INR, Platelet count)

Sponsors

Goethe University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years

Inclusion criteria

* Platelet count \> 100 / nll * In study group and control group 1: Week of Pregnancy: 35-40 * in control group 2: healthy, not pregnant woman

Exclusion criteria

* Hereditary coagulopathy * Missing content of the patient / proband * Eclampsia * HELLP syndrome * CRP \> 1 mg/dl * Fever (\> 38°C)

Design outcomes

Primary

MeasureTime frameDescription
Area under the aggregation curve in the ADPtest of the Multiple Electrode AggregometryBetween 35th and 40th week of pregnancy; in control group 2 (not pregnant) within 1 week after inclusion into the studyADP induced platelet aggregation

Secondary

MeasureTime frameDescription
Area under the aggregation curve in the ASPItest of the Multiple Electrode AggregometryBetween 35th and 40th week of pregnancy; in control group 2 (not pregnant) within 1 week after inclusion into the studyArachidonic acid induced platelet aggregation
Area under the aggregation curve in the TRAPtest of the Multiple Electrode AggregometryBetween 35th and 40th week of pregnancy; in control group 2 (not pregnant) within 1 week after inclusion into the studyThrombin induced platelet aggregation
Parameters of plasmatic coagulation systemBetween 35th and 40th week of pregnancy; in control group 2 (not pregnant) within 1 week after inclusion into the studyvon Willebrand Factor, Factor VIII, Factor XIII, parameter of conventional coagulation testing (apTT, INR, platelet count, Fibrinogen)

Contacts

Primary ContactChristian F Weber, MD, PhD
christian.weber@kgu.de+49 69 6301 5514
Backup ContactNiels Loechelt, MD
niels.loechelt@kgu.de+49 69 6301 5514

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026