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Serial Body Composition Measurements by PEAPOD

NCT07926620, Not yet recruiting, Shoklo Malaria Research Unit

Trial 9

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

FieldValueSource
TitleSerial Body Composition Measurements by PEAPODClinicalTrials.gov
NCT numberNCT07926620ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
Enrollment300 participants, estimatedClinicalTrials.gov
Lead sponsorShoklo Malaria Research UnitClinicalTrials.gov
ConditionsInfant, Small for Gestational Age, Body Composition, Infant GrowthClinicalTrials.gov
InterventionsPEAPOD Air Displacement Plethysmography DeviceClinicalTrials.gov
First posted2026-11-09ClinicalTrials.gov
Last updated2026-11-09ClinicalTrials.gov

Registered outcomes 11

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescriptionSource
PrimaryBody composition changes - Fat mass in neonates with small for gestational age (SGA) and appropriate for gestational age (AGA) at birth and during the first 6 months of lifeAt birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)
Fat mass (kg) measured using air displacement plethysmography (PEAPOD) at birth and during follow-up visits to compare between small for gestational age (SGA) and appropriate for gestational age (AGA) infants
ClinicalTrials.gov
PrimaryBody composition changes - Fat-free mass in neonates with small for gestational age (SGA) and appropriate for gestational age (AGA) at birth and during the first 6 months of lifeAt birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)Fat-free mass (kg) measured using PEAPOD at birth and during follow-up visits to compare between SGA and AGA infantsClinicalTrials.gov
PrimaryPercentage body fat in SGA and AGA infantsAt birth, 1, 2, 3, 4, 5 and 6 months of life (unless body weight >6.0kg is reached first)Percentage body fat (%) measured using PEAPOD at birth and during follow-up visits to compare between SGA and AGA infantsClinicalTrials.gov
SecondaryMaternal First-Trimester Body Mass Index (BMI)Baseline (antenatal records)Maternal first-trimester BMI (kg/m²) calculated from weight and height recorded during antenatal careClinicalTrials.gov
SecondaryMaternal Gestational Weight GainBaseline (antenatal records)Maternal gestational weight gain (kg) calculated from antenatal weight measurementsClinicalTrials.gov
SecondaryGestational Diabetes Mellitus StatusBaseline (antenatal records)Presence or absence of gestational diabetes mellitus documented in maternal clinical recordsClinicalTrials.gov
SecondaryMaternal AnaemiaBaseline to maximum 6 months postpartumPresence or absence of maternal anaemia determined from maternal haemoglobin measurementsClinicalTrials.gov
SecondaryMaternal HbA1c ConcentrationDelivery and 2 months postpartumMaternal glycated haemoglobin (HbA1c) percentage (%) measured from maternal blood samplesClinicalTrials.gov
SecondaryBreast Milk CreamatocritAt birth to maximum 6 months postpartumCreamatocrit percentage (%) measured from maternal breast milk samplesClinicalTrials.gov
SecondaryBreast Milk Sodium ConcentrationAt birth to maximum 6 months postpartumSodium concentration (mmol/L) measured from maternal breast milk samplesClinicalTrials.gov
SecondaryBreast Milk Proteomic ProfileDelivery and monthly postpartum until 6 monthsProteomic profile of maternal breast milk measured using MALDI-TOF analysisClinicalTrials.gov

Outcomes 0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

Grants 0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

ComparisonSource

Tests 0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed asSource

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

Release trials-2026-11-12-0.4.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)