Trials / Recruiting
RecruitingNCT04720690
Bioimpedence and Arterial Function Monitoring at Birth and in Infants
Bioimpedence and Arterial Function Monitoring at Birth and in Infants: the BAMBI Study
- Status
- Recruiting
- Phase
- —
- Study type
- Observational
- Enrollment
- 120 (estimated)
- Sponsor
- Imperial College Healthcare NHS Trust · Academic / Other
- Sex
- All
- Age
- 6 Months
- Healthy volunteers
- Accepted
Summary
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.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | Vicorder: pulse wave velocity, pulse wave analysis, stroke volume, cardiac output | Measurement of arterial stiffness and cardiac output |
| DEVICE | NICaS | Measurement of cardiac output |
| DEVICE | Echocardiography and ultrasound of arteries | Measurement of cardiac output; measurement of intima-media thickness of arteries |
Timeline
- Start date
- 2020-12-01
- Primary completion
- 2024-12-31
- Completion
- 2024-12-31
- First posted
- 2021-01-22
- Last updated
- 2024-07-29
Locations
2 sites across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT04720690. Inclusion in this directory is not an endorsement.