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Portal Vein Pulsatility Flow in Pregnancy

Portal Vein Pulsatility Flow in Pregnancy - a Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04429178
Enrollment
80
Registered
2020-06-12
Start date
2020-08-13
Completion date
2022-03-01
Last updated
2022-03-02

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

Conditions

Pregnancy

Keywords

portal vein pulsatility, physiologic volume overload

Brief summary

This study is to investigate if portal vein pulsatility fraction can be measured in pregnancy and if it increases during the course of pregnancy as would be expected by the physiologic increase in blood volume that happens during pregnancy. Portal vein pulsatility fraction is measured in non-pregnant controls and in women in the 1st, 2nd and 3rd trimester of pregnancy.

Interventions

OTHERultrasound

portal vein pulsatility fraction (percent) measured with ultrasound

Sponsors

University Hospital, Basel, Switzerland
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* Ability to give informed consent * American Society of Anesthesiologists (ASA) Class I and II * Singleton pregnancy during 1st, 2nd or 3rd trimester or healthy non-pregnant females of childbearing age as controls

Exclusion criteria

* Inability to give informed consent * Multiple gestation * Significant co-morbidities (e.g. cardiac abnormalities, cardiac dysfunction, arrhythmias, severe asthma, renal insufficiency) * High risk pregnancies (e.g. pre-eclampsia, gestational hypertension, HELLP, gestational diabetes) * Body-Mass-Index (BMI) \< 18kg/m2 or \>40kg/m2

Design outcomes

Primary

MeasureTime frameDescription
Portal vein pulsatility fraction (percent)single time-point at baselinePortal vein pulsatility fraction (percent)

Secondary

MeasureTime frameDescription
Inferior vena cava diameter (mm)single time-point at baselineInferior vena cava diameter (mm)
Inferior vena cava collapsibility index (percent)single time-point at baselineInferior vena cava collapsibility index (percent)
Hepatic venous flow (cm/sec)single time-point at baselineHepatic venous flow (cm/sec)
Right atrial and ventricular dimensions (cm)single time-point at baselineRight atrial and ventricular dimensions (cm)
Tricuspid Annular Plane Systolic Excursion (TAPSE) (mm)single time-point at baselineTricuspid Annular Plane Systolic Excursion (TAPSE) (mm)

Countries

Switzerland

Outcome results

None listed

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