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Evaluation of Electrical Velocimetry for Assessment of Extra-vascular Lung Water in Pre-eclamptic Patients

Evaluation of Electrical Velocimetry for Assessment of Extra-vascular Lung Water in Pre-eclamptic Patients

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03127865
Enrollment
60
Registered
2017-04-25
Start date
2017-04-18
Completion date
2017-08-16
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

Pre-Eclampsia

Brief summary

The purpose of this study is to compare the sensitivity and the specificity of electrical cardiometry to the lung ultrasound in measuring thoracic lung water in pregnant females with pre-eclampsia. If electrical cardiometry is validated against ultrasound, it will be easy to use with numerical number that will not require advanced experience as with the ultrasound.

Detailed description

Pre-eclampsia is accompanied with increased risk of serious complications such as pulmonary edema, cerebrovascular accidents, coagulopathy, and hemorrhage. Pre-eclampsia is responsible for 46.6% of the etiology of acute pulmonary edema in pregnant women. Fluid management in pre-eclamptic patients is challenging. Hypovolemia exacerbates organ failure, whereas volume overload results in pulmonary edema. Thus, using different methods for evaluation of volume status of the patients would improve patient management. Lung ultrasound has been developed as an accurate non-invasive method for assessment of extra-vascular lung water; However, ultrasound needs skilled operator. Electrical velocimetry (cardiometry) is a newer technology for assessment of total thoracic fluid content (TFC); however, it has not been validated in pre-eclamptic patients. In this study the investigators will validate the accuracy of cardiometry in evaluation of lung water using the lung ultrasound as a gold standard. Both methods will be evaluated for prediction of the need of diuretic therapy and the need for post-operative oxygen therapy.

Interventions

None listed

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* pregnant * pre-eclamptic * In first stage of labor

Exclusion criteria

* Eclampsia. * Second, third and fourth stages of labor on admission. * Patients with severe cardiac and/or pulmonary disease.

Design outcomes

Primary

MeasureTime frameDescription
total thoracic fluid contentafter 30 minutes from patient admission to the obstetric casualitytotal fluid content measured by electrical velocimetry device (cardiometry)

Secondary

MeasureTime frameDescription
extra-vascular lung waterafter 30 minutes from patient admission to the obstetric casualityextra-vascular lung water measured by ultrasound (lung ultrasound score)
lung congestionduring the period starting from admission till one day after deliverythe presence of lung congestion manifested by audible crepitations by chest auscultation
The need of diureticsduring the period starting from admission till one day after deliveryThe presence of lung congestion manifested by respiratory distress (dyspnea, tachypnea, and decreased oxygen saturation below 90%) needing intravenous diuretics
arterial blood pressureafter 30 minutes from patient admission to the obstetric casualityarterial blood pressure measured in mmHg
heart rateafter 30 minutes from patient admission to the obstetric casualitythe number of heart beats per minute
serum albuminafter 30 minutes from patient admission to the obstetric casualitythe level of albumin in blood (measured by g/ liter

Countries

Egypt

Outcome results

None listed

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