ClinicalTrials.gg
RecruitingNCT07760194Updated Aug 13, 2026

Evaluation of Fetal Heart

An observational study in Fetal Growth Restriction, sponsored by Assiut University. Recruiting at 1 site in Egypt. Open to female participants, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-08-13.

Sponsored by Assiut University · Observational

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Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
28
Sex
Female
01

Where this study stands

Counted across the records on this site · 2026-11-14

Among 10 studies in Fetal Growth Retardation by Assiut University — 3 open to participants now, 3 under way, none of them phase 3. Fetal Growth Retardation · Assiut University.

Started
2026
with 2 others
Observational
6 of 10
3 open now
Registered
10th of 10
by date

Among the 10 studies in Fetal Growth Retardation by Assiut University, this one is one of 3 that started in 2026, is one of 6 observational ones, and was the 10th registered.

Fetal Growth Retardation

262 studies on the registry are indexed under Fetal Growth Retardation; 69 are open to participants now.

Browse Fetal Growth Retardation studies →

Open to participants now

3 of the 10 studies in Fetal Growth Retardation by Assiut University are open now, in 1 country. Recruiting first, the newest first:

By country, each count listing its studies:

All 3 open studies →

Where they have run

Who these studies take

Of the 48 Fetal Growth Retardation studies recruiting now, 24 (50%) set no upper age limit and 21 (44%) stop at 75 or younger; 16 take children under 18; 24 take healthy volunteers.

This study: female · healthy volunteers too.

The full table on the hub →

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02

Study summary

Evaluation of fetal cardiac functions in cases complicated with growth restriction

Read the detailed description

10% of pregnancies are, by the description, affected by the common obstetric issue known as intrauterine growth restriction (IUGR). IUGR is a significant contributor to prenatal mortality and morbidity. Cardiomyopathy is a reliable marker of the advancement of IUGR; in these babies, it begins during the early phases of fetal growth restriction and worsens as fetal impairment advances. IUGR is caused by placental dysfunction and this leads to a state of chronic hypoxia and metabolic stress and redistribution of blood flow towards vital organs, such as the brain, heart and adrenal glands. This hemodynamic compensation can itself contribute to a progressive deterioration of fetal cardiac function and myocardial remodeling. The myocardial performance index (MPI), also known as the Tei index, has emerged as a promising tool for the non-invasive evaluation of global fetal cardiac function, integrating both systolic and diastolic performance. To overcome some of the reproducibility-related limitations of the original technique, a modified version of the MPI (Mod-MPI) was introduced, which uses the opening and closing 'clicks' of the heart valves as more precise temporal landmarks. In recent years, numerous studies have investigated the role of MPI in the assessment of IUGR fetuses, and have suggested that this index may be altered early in gestation in response to chronic hypoxia and hemodynamic stress.

03

Conditions studied

  • Fetal Growth Restriction

Keywords

  • Fetal heart
  • Echocardiography
  • IUGR
04

Who can participate

Ages eligible
Child (0–17), Adult (18–64), Older adult (65+)
Sexes eligible
Female
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

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

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Inclusion criteria

  • pregnant women
  • more than 28 weehs gestation

Exclusion criteria

Exclusion Criteria:

  • intrauterine fetal death
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
28 participants (estimated)
Patient registry
No

Groups and cohorts

  • Cases with IUGR

    Fetal weight less than 10th percentile

    Procedure: Echocardiography

  • Cases with normal growth

    Fetal weight between 10th and 90th percentile

    Procedure: Echocardiography

Interventions

  • ProcedureEchocardiography

    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

06

What researchers measure

Primary outcomes

  1. Measurement of MPI

    Increased MPI means bad outcome

    Time frame: 2 weeks

07

Study locations

1 of 1 sites recruiting
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reachedSimilar studies: half by the dot; the band is the middle halfHalf of similar studies reached it by the dot; the band is the middle half, from a quarter to three quarters

Start is estimated for Aug 2026; primary completion for Sep 2026, 1 month later.

Of 72 non-industry observational studies under Fetal Growth Retardation, half reached primary completion within 52 months of starting (the median), counting those still running; a quarter within 24 and three quarters within 170. This study's planned 1 month is below that.

Counting every sponsor, half of 73 studies reached it within 52 months; a quarter within 24 and three quarters within 170.

How these figures are worked out, and which studies are left out of them.

Registered
Aug 7, 2026
First posted
Aug 12, 2026
StartEst.
Aug 2026
Primary completionEst.
Sep 2026
CompletionEst.
Sep 2026
Last update
Aug 13, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Aug 13, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT07760194
Lead sponsor
Assiut University
Responsible party
Mohamed Gamal M.fekry (Lecturer of obstetrics and gynecology, Assiut University) — Principal investigator
First posted
Aug 12, 2026
Start date
Aug 2026 (estimated)
Primary completion
Sep 2026 (estimated)
Completion
Sep 2026 (estimated)
Last update
Aug 13, 2026

Study contacts

Mohamed Fekry
Contact
mohamedbeethoven2040@gmail.com
+20882312388

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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