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A Study to Assess Metabolic Bone Disease of Prematurity Using an Acoustic Method

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Mayo Clinic

Status

Completed

Conditions

Osteopenia
Metabolic Bone Disease
Neonatal Rickets

Treatments

Diagnostic Test: Vibro-acoustic analysis (VAA), based on ultrasound radiation force

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT04752098
19-001498
5R21AR075370-02 (U.S. NIH Grant/Contract)
1R21AR075370-01A1 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

The goal of this project is to develop a new noninvasive ultrasound based technique, called vibro-acoustic analysis (VAA), for evaluation of infant bone health with particular application in assessment of bone health in premature infants who are at risk for bone disease.

Full description

With increased survival of very low birth weight and premature infants over recent decades, bone assessment has become especially vital with the recognition of metabolic bone disease (MBD) of prematurity. Bone assessment became especially vital during last decades with the growing emphasis on metabolic bone disease of prematurity and low-birth-weight infants. Statistics shows that up to 50% of low birth weight and preterm newborns are likely to develop metabolic bone disease. Currently, no screening test has been shown to provide both sensitive and specific evidence of developing MBD over the first several weeks of life in the premature infants. Therefore, there is a need for a non-invasive tool for evaluation of infant bone health. This study will be conducted on premature infants at risk for MBD at multiple time points during their growth, with full term infants as controls. vibro-acoustic analysis (VAA) measurements will be done on the tibia. VAA measurements for the premature infants will be compared to those of full term infants. Performance of VAA in identifying osteopenia and its ability to monitor the response to treatment will be evaluated. The investigators will use an ultrasound system that has been used in the pilot study and employ a transducer with a smaller footprint for pediatric application.

Enrollment

37 patients

Sex

All

Ages

3 days to 8 months old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Full term newborns, approximately equal number of male and female newborn, age <28 days.
  • Preterm infants, approximately equal number of male and female preterm infants with gestational age at birth <37 weeks or birth weight <1500 grams.

Exclusion criteria

  • Infants currently requiring continuous cardiovascular medication infusions, including but not limited to, dopamine, epinephrine, milrinone, and dobutamine (may have received these medications in the past.
  • Infants with major congenital anomalies that may affect bone health or structure.
  • For full term infants, infants with a history of intrauterine growth restriction or who are small for gestational age (<10th percentile for weight) at birth.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

37 participants in 1 patient group

premature infants and full term infants
Other group
Description:
The study visits will be at ≥3 time points at ages: within the first 28 days after birth, 2 months, 3 months, and, if still hospitalized, at 4 months and at 6 months. * The ultrasound machine to the nursery or neonatal intensive care unit at a scheduled time. * The appropriate ultrasound probe will be placed on the infant's tibia and a miniature hydrophone near the probe. A series of ultrasound measurements will be obtained and the ultrasound data will be saved for offline processing. * The Investigators will repeat the measurement in 3 locations of the infant's tibia. * Each ultrasound measurement takes a few seconds. The complete ultrasound study will take about 15 minutes at each visit. * All procedures will be conducted in the nursery or neonatal intensive care unit to ensure infant safety. * The ultrasound measurement for full-term infants can be done in ultrasound lab.
Treatment:
Diagnostic Test: Vibro-acoustic analysis (VAA), based on ultrasound radiation force

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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