Cardiac Displacement From Third Trimester to Early Childhood (CADETTE)

March 30, 2021 updated by: Olov Änghagen, University Hospital, Linkoeping
The aim is to increase awareness of the relationship between (IUGR) and cardiac function in the foetus, the development of cardiac function over time after delivery and what significance a possible early disturbed myocardial function have for the neonate and the child during the first years of life.

Study Overview

Detailed Description

This is a prospective case-control study in which fetuses from normal pregnancies will be compared with fetuses with IUGR. Parents will be asked to participate in the study in connection with the routine ultrasound examinations at the department of obstetrics to where they have been referred because of suspected IUGR. The control group will be randomly selected among pregnant women who come for routine ultrasound during pregnancy at gestational week 18-20.

Surveys will be performed in the third trimester and after delivery. During the ultrasound examinations standardized, moving sequences of the heart will be saved. Analyses will be performed off-line and analysed by vector velocity imaging software. With this technique, the investigator can quantify the chamber wall and myocardial movements. Speed (velocity), movement (displacement) and thickening/deformation (strain and strain rate) will be recorded in a structured and standardized manner.

When performing the analysis the heart's walls are outlined and the software extracts the movement in different directions.

Data will be obtained concerning the participating mothers previous illness, mothers' age, maternal smoking, BMI, any abnormalities during pregnancy, number of previous pregnancies. Other data that will be recorded are means of delivery and any abnormalities during previous pregnancies, such as hypertension, preeclampsia and pre-natal steroid treatment.

Additional data to be collected from the participating fetuses are flow profiles in the umbilical artery, ductus venosus and middle cerebral artery. Abdominal circumference and estimated weight will be registered.

Following delivery, the participating child's height, weight, head circumference and gestational age at birth are registered. Additional data that will be collected after delivery are umbilical vein and umbilical artery acid base values, Apgar score. If admitted to the pediatric ward the investigators will register the number of days hospitalized in the ward for post-natal care and diagnosis. The investigators plan to examine the participating baby with cardiac ultrasound between 12 and 72 hours after delivery and again when the participating child is 3-4 months old and at 7 years of age.

The investigators will take a blood sample from the umbilical cord at birth and again at 7 years of age. The investigators will analyse the blood for growth factors and cardiac markers. An additional ethical approval was accepted 2015 for analysing epigenetic factors in the participating children's DNA.

Based on power calculation the investigators plan to examine between 20-30 fetuses with IUGR and 40-60 healthy fetuses in the control group.

Study Type

Observational

Enrollment (Anticipated)

90

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Linköping, Sweden, 58185
        • Dept of Obstetrics and Gynecology
      • Linköping, Sweden, 59071
        • Paediatric Department University Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Child
  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

This is a prospective case-control study in which fetuses from normal pregnancies will be compared with fetuses with IUGR. Parents will be asked to participate in the study in connection with the routine ultrasound examinations at the department of obstetrics to where they have been referred because of suspected IUGR. The control group will be randomly selected among pregnant women who come for routine ultrasound during pregnancy at gestational week 18-20.

Description

Inclusion Criteria:

  • Inclusion of research subjects: Growth restriction in routine pregnancy ultrasound, verified by specialist control. Gestational age based on Crown Rump Length measurements during the first trimester. Growth restriction defined by a deviation more than 22% from the normal curve at a given gestational age or growth rate deviates more than 10% compared to the previous measurement in relation to the expected weight.
  • Inclusion of controls: Control individuals recruited among mothers who come to routine pregnancy ultrasound control at gestational week 18. These are randomly selected and then asked to participate.

Exclusion Criteria:

  • Exclusion of both the cases with IUGR and the control cases are major malformations, twin pregnancy, signs of intrauterine infection during pregnancy, significant illness or significant medical treatment of the mother.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Fetuses/Children with IUGR

The moving sequences of the heart movement are collected at the regular ultrasound examinations during pregnancy. Following delivery the investigators plan to examine the baby with cardiac ultrasound, echocardiography, between 12 and 72 hours after delivery and again when the child is 3-4 months old and at 7 years of age.

Blood sample will be taken from the umbilical cord at birth and again at 7 years of age. The investigators will analyse the blood for growth factors and cardiac markers. An additional ethical approval was accepted 2015 for analysing epigenetic factors in the children's DNA.

During the ultrasound examinations standardized, moving sequences of the heart will be saved. Analyzes are performed off-line and analyzed by vector velocity imaging software.
The investigators will take a blood sample from the umbilical cord at birth and again at 7 years of age.
Healthy Controls

The moving sequences of the heart movement are collected at two occasions approximately 4 weeks apart. This takes place during gestational weeks 28-36. Following delivery the investigators plan to examine the baby with cardiac ultrasound, echocardiography, between 12 and 72 hours after delivery and again when the child is 3-4 months old and at 7 years of age.

Blood sample will be taken from the umbilical cord at birth and again at 7 years of age. The investigators will analyze the blood for growth factors and cardiac markers. An additional ethical approval was accepted 2015 for analysing epigenetic factors in the children's DNA.

During the ultrasound examinations standardized, moving sequences of the heart will be saved. Analyzes are performed off-line and analyzed by vector velocity imaging software.
The investigators will take a blood sample from the umbilical cord at birth and again at 7 years of age.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Velocity of the cardiac walls
Time Frame: At least two times before delivery from gestational age 28 weeks to delivery. Three times after delivery, 12-72 hours, 3-4 months and 7 years.
Echocardiography images of the heart's walls are outlined and the software extracts the movement in different directions.
At least two times before delivery from gestational age 28 weeks to delivery. Three times after delivery, 12-72 hours, 3-4 months and 7 years.

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Displacement of the cardiac walls
Time Frame: At least two times before delivery from gestational age 28 weeks to delivery. Three times after delivery, 12-72 hours, 3-4 months and 7 years.
Echocardiography images of the heart's walls are outlined and the software extracts the movement in different directions.
At least two times before delivery from gestational age 28 weeks to delivery. Three times after delivery, 12-72 hours, 3-4 months and 7 years.
Strain in the cardiac walls
Time Frame: At least two times before delivery from gestational age 28 weeks to delivery. Three times after delivery, 12-72 hours, 3-4 months and 7 years.
Echocardiography images of the heart's walls are outlined and the software extracts the movement in different directions.
At least two times before delivery from gestational age 28 weeks to delivery. Three times after delivery, 12-72 hours, 3-4 months and 7 years.
Cardiac marker Troponin T
Time Frame: At birth and at 7 years of age
Comparing cardiac marker troponin T between the two groups
At birth and at 7 years of age
Cardiac marker N-terminal prohormone of brain natriuretic peptide (NT-ProBNP)
Time Frame: At birth and at 7 years of age
Comparing cardiac marker NT-ProBNP between the two groups
At birth and at 7 years of age
Insulin-like growth factor-1 (IGF-1)
Time Frame: At birth and at 7 years of age
Comparing IGF-1 between the two groups
At birth and at 7 years of age
Insulin-like growth factor binding protein (IGFBP)
Time Frame: At birth and at 7 years of age
Comparing IGFBP between the two groups
At birth and at 7 years of age
DNA methylation and gene expression in blood monocytes and lumfocytes
Time Frame: At birth and at 7 years of age
Changes in DNA metylation will be compared between the two groups
At birth and at 7 years of age

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Olov Änghagen, PhD student, Dept of Paediatric, Linköping
  • Study Chair: Nina Nelson, Professor, Karolinska University Hospital, Stockholm
  • Study Chair: Peter Bang, Professor, Dept of Paediatric, Linköping
  • Study Chair: Jan Engvall, Professor, Dept of Clinical Physiology, Linköping
  • Study Chair: Eva Nylander, Professor, Dept of Clinical Physiology, Linköping

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

January 1, 2013

Primary Completion (Anticipated)

December 1, 2023

Study Completion (Anticipated)

December 1, 2023

Study Registration Dates

First Submitted

October 16, 2015

First Submitted That Met QC Criteria

October 20, 2015

First Posted (Estimate)

October 22, 2015

Study Record Updates

Last Update Posted (Actual)

April 1, 2021

Last Update Submitted That Met QC Criteria

March 30, 2021

Last Verified

March 1, 2021

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Fetal Growth Retardation

Clinical Trials on Echocardiography

3
Subscribe