Bioimpedence and Arterial Function Monitoring at Birth and in Infants

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 6
SponsorImperial College Healthcare NHS Trust

About this trial

Babies may be born appropriately grown for gestational age (AGA, \>10th centile) or small for gestational age (SGA, \<10th centile). Babies who are SGA and have evidence in utero of vascular compromise using antenatal doppler indices are classified as having fetal growth restriction (FGR). Babies with FGR are at increased risk of cardiovascular disease in adult life. Increased arterial stiffness and intima-media thickness are thought to mediate this risk in adults. It is not known how early in life these changes can be robustly detected. In addition, very little is known generally about how babies' hearts and arteries change in structure and function over the first year of life, whether affected by SGA or not. This study aims to understand if there are differences in cardiac and arterial structure and function between babies born AGA or SGA. Within the group of SGA babies, the study team will investigate whether FGR and maternal pre-eclampsia influence these measurements. The effects gestational age on these parameters will be studied within all groups: half of the babies recruited will be \<32 weeks gestational age (GA), and half will be ≥32 weeks GA. Study participants will have further measurements at 3-6 months of life to assess if cardiac and arterial structure and function change in babies over the first year of life. The study team will use the Vicorder device to measure arterial stiffness, and assess the feasibility of using this device in neonates. The Vicorder will also be used to measure cardiac output. The feasibility and validity of this device for this purpose will be investigated (Vicorder is not validated for cardiac output measurement in infants). Vicorder cardiac output results will be compared to echocardiography and bioimpedence technology (using the NICaS monitor). The study team will use ultrasound for arterial structure measurements of the carotid artery and aorta.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy term infants (including those with SGA+/-FGR) in the postnatal ward

Term and Preterm infants (including those with SGA+/-FGR) admitted to the neonatal unit

Written informed parental consent

Disqualifiers

Antenatal or postnatal diagnosis of complex/life-limiting congenital anomaly or genetic condition

Infants with no realistic chance of survival

Infants with fragile skin not permitting use of cuffs for research purposes

Babies whose parents have a limited understanding of English will be excluded in the event that communication via NHS translation services is not possible due to clinical demands on these services

Trial population

All term and preterm infants born at the Imperial College Healthcare NHS trust can be included to the study after parental consent.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Vicorder: pulse wave velocity, pulse wave analysis, stroke volume, cardiac output

    Device

    Measurement of arterial stiffness and cardiac output

  • NICaS

    Device

    Measurement of cardiac output

  • Echocardiography and ultrasound of arteries

    Device

    Measurement of cardiac output; measurement of intima-media thickness of arteries

Treatment groups

120 Participants
are divided into 3 treatment groups
Group A: Appropriately grown for age infants3 interventions
Group B: Small for gestational age infants3 interventions
Group C: Fetal growth restricted infants3 interventions

Trial outcomes

Primary outcomes

1

Feasibility of arterial and cardiac function measurements: the proportion of babies from whom study measurements are successfully obtained.

Feasibility of arterial and cardiac function measurements assessed through establishing from what proportion of babies the team is able to successfully obtain these measurements.

Time frame
3 years

Secondary outcomes

1

Non-invasive measurement of arterial stiffness: brachial-femoral pulse wave velocity

Brachial-femoral pulse wave velocity in metres per second (m/s) will be measured using the Vicorder and compared between neonates of different gestational age and birth weight groups at or near term corrected gestational age, and at 3-6 months of age.

Time frame
3 years
2

Non-invasive measurement of arterial stiffness: augmentation index

Augmentation index (%) will be measured using the Vicorder and compared between neonates of different gestational age and birth weight groups at or near term corrected gestational age, and at 3-6 months of age.

Time frame
3 years
3

Arterial structure measurements

The intima-media thickness of the carotid artery and abdominal aorta will be measured in micrometres (µm) using ultrasound at or near term corrected gestational age, and at 3-6 months of age. Gestational age and birth weight groups will be compared at each time point.

Time frame
3 years
4

Cardiac output measurements: comparison of neonatal and infant birth weight and gestational age cohorts

Cardiac output in L/min and ml/min/kg will be measured using echocardiography, the NICaS monitor and the Vicorder. Values obtained in different gestational age and birth weight groups will be compared at or near term corrected gestational age and at 3-6 months of age.

Time frame
3 years

Other outcomes

Sponsors and contacts

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