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NCT Number: NCT04720690

Bioimpedence and Arterial Function Monitoring at Birth and in Infants

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.

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Key information

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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

Exclusion criteria

  • 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

Treatment and study plan

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

Primary outcomes

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

    Time frame: 3 years

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

Secondary outcomes

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

    Time frame: 3 years

    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.

  2. Non-invasive measurement of arterial stiffness: augmentation index

    Time frame: 3 years

    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.

  3. Arterial structure measurements

    Time frame: 3 years

    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.

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

    Time frame: 3 years

    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.

  5. Cardiac output measurements: comparison of devices

    Time frame: 3 years

    Cardiac output values in L/min and ml/min/kg obtained by each device (echocardiography, NICaS monitor and Vicorder) will be compared using correlation and Bland-Altman statistics.

Study contacts

Contact information is provided by the study sponsor or research team.

Jayanta Banerjee, MD (Res), FRCPCH

CONTACT

[email protected]

020 3313 7308

Sponsors and collaborators

Lead sponsor

Imperial College Healthcare NHS Trust

Other

Registry information

Official study title

Bioimpedence and Arterial Function Monitoring at Birth and in Infants: the BAMBI Study

Acronym: BAMBI

Important dates

Study start
2020
Primary completion
2024
Study completion
2024
First posted
Jan 22, 2021
Registry last updated
Jul 29, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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