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Measurement of in Vivo Mitochondrial Capacity in Infants | Clinical Trials | Clareo Health

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Measurement of in Vivo Mitochondrial Capacity in Infants

Measurement of in Vivo Mitochondrial Capacity in Infants: a 31P-MRS Pilot Study

NCT03976596•Pennington Biomedical Research Center

Summary

The overarching aim of this project is to determine the test re-test reliability of 31P-magnetic resonance spectroscopy measurements in infants. Primary endpoints include two separate measures of in vivo mitochondrial capacity (ATPmax) over a 1-10 day period to assess feasibility and reliability.

Eligibility

Age

0 - 0 years

Sex

ALL

Healthy Volunteers

Yes

Inclusion Criteria

•healthy, full-term infant
•aged 14-28 days at Visit 1
•willingness of parents to be notified of incidental findings from study procedures

Exclusion Criteria

•born preterm
•implanted metal or electronic objects that render MRI unsafe
•unable to complete 2 clinic visits 1-10 days apart at Pennington Biomedical Research Center

Locations (1)

Pennington Biomedical Research Center

Baton Rouge, Louisiana, United States

Key Dates

Start Date

May 21, 2019

Primary Completion Date

July 2, 2019

Completion Date

July 2, 2019

Last Updated

February 3, 2026

Enrollment

ACTUAL participants

Conditions

Healthy Infants

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: February 3, 2026Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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