Evaluation of Fetal Heart

ConditionFetal Growth Restriction

Trial statusRecruiting

Trial phaseNot listed

Trial typeObservational

Biological sexFemale

AgeNot listed

SponsorAssiut University

About this trial

Evaluation of fetal cardiac functions in cases complicated with growth restriction

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

pregnant women

more than 28 weehs gestation

Disqualifiers

intrauterine fetal death

Trial population

Fetuses with IUGR will be included in group 1. Fetuses with normal growth will be included in group 2.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Echocardiography
Procedure/Surgery
Modified MPI is obtained by placing the Doppler sample volume on the medial wall of the ascending aorta including the AV and MV, hence the movements of both valves are recorded simultaneously in the Doppler spectrum through measurements of the isovolumetric contraction time (ICT), isovolumetric relaxation time (IRT) and ejection time (ET). The isovolumetric contraction time (ICT) was measured from the closure of the MV to the opening of the AV, the ejection time (ET) from the opening to the closure of the AV, and the isovolumetric relaxation time (IRT) from the closure of the AV to the opening of the MV. The MPI (Tei index) was calculated using the following equation: MPI= (ICT + IRT)/ET

Treatment groups

28 Participants

are divided into 2 treatment groups

Group A: Cases with IUGR1 intervention

Group B: Cases with normal growth1 intervention

Trial outcomes

Primary outcomes

Measurement of MPI

Increased MPI means bad outcome

Time frame

2 weeks

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Assiut University

Lead sponsor

Source ClinicalTrials.gov

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