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Echocardiographic Assessment of Ventricular Strain During a Healthy Pregnancy in the First, Second, and Third Trimester.

NCT04395014 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 50

Last updated 2020-05-20

No results posted yet for this study

Summary

Pregnancy is a physiological situation that produces transient preload and afterload changes. The heart is subjected to reversible morphological remodelings and hemodynamic and functional adaptations. The characterization and understanding of maternal cardiac function during normal pregnancy by echocardiography 2D is of clinical importance for the opportune recognition of cardiac pathology.

This study aims to investigate pregnancy-induced changes in ventricular strain in healthy pregnant women by echocardiography.

Conditions

  • Echocardiography
  • Pregnancy Related Conditions, Unspecified, First Trimester
  • Pregnancy Related Conditions, Unspecified, Second Trimester
  • Pregnancy Related Conditions, Unspecified, Third Trimester
  • Ventricle Remodeling

Interventions

DIAGNOSTIC_TEST

2D Echocardiography

In this echocardiographic imaging acquisition protocol, the pregnancy patients, are colocated in the left lateral decubitus position on a clinical bed with the left arm flex and the hand behind the head. All the echocardiographic measurements are taken by the examiner in this position.

Sponsors & Collaborators

  • Leiden University Medical Center

    collaborator OTHER

  • Institute of Security and Social Services of Workers of the State of Puebla.

    collaborator UNKNOWN

  • Miguel Ayala León

    lead NETWORK

Eligibility

Min Age
20 Years
Max Age
35 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2020-10-01
Primary Completion
2020-12-01
Completion
2021-08-31

Countries

  • Mexico

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT04395014 on ClinicalTrials.gov