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Determination of Clinical Phenotypes of Intrauterine Growth Restriction in Term Infants Based on Body Composition

Determination of Clinical Phenotypes of Intrauterine Growth Restriction in Term Infants Based on Body Composition. A Potential Contribution to Nutritional Management.

Status
Enrolling by invitation
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07483424
Acronym
Restrigrowth
Enrollment
290
Registered
2026-03-19
Start date
2025-11-19
Completion date
2028-06-30
Last updated
2026-04-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Intrauterine Growth Restriction (IUGR)

Keywords

Doppler velocimetry, fetal growth, intrauterine growth restriction, nutritional management, small for gestational age

Brief summary

Intrauterine growth restriction (IUGR) is defined as the inability of the fetus to fulfill its genetic growth potential. "Small for gestational age" (SGA) is the most commonly used indicator for diagnosing IUGR. However, this definition does not consider intrauterine growth trajectory or physical characteristics at birth. SGA is based on the relationship between birth weight and gestational age, and does not address anthropometric measurements at birth or prenatal indicators, such as biometric, biophysical, and Doppler velocimetry abnormalities. SGA infants may constitute intrauterine growth restricted as well as constitutionally small infants. This distinction can be made more accurately by complementary assessment of body composition. The clinical meaning of each group identified by body composition will be assessed by the evolution until 3-months of age. The feeding pattern and composition will be considered a major postnatal exposure. Accurate classification of IUGR profiles is essential to ensure appropriate nutritional intervention.

Detailed description

Study design: This is a single-center prospective observational, cohort study of full-term infants born with intrauterine growth restriction (IUGR) and their lactating mothers. Study period: A consecutive recruitment of participants will be conducted over 18 months (from November 19, 2025). Eligible children, whose parents accepted the invitation to participate, will be recruited in a follow-up study until they are 3 months old. Settings: Neonatology Unit, Prenatal Diagnostic Center and Human Milk Bank at Maternidade Dr. Alfredo da Costa, Unidade Local de Saúde São José, Lisbon. Nutrition Laboratory of Hospital Dona Estefânia, Unidade Local de Saúde São José, Lisbon, Portugal. Variables in study: * Mother's retrieved demographic and clinical variables will include: mother's age, height, reported body weight closer to the beginning of pregnancy, body weight gain during pregnancy, pathological conditions during pregnancy (diabetes mellitus type I and type II, gestational diabetes, gestational hypertension, hypertension, pre-eclampsia, chronic renal disease, systemic lupus erythematosus, anaemia or other conditions). * Obstetrics' Doppler velocimetry serial ultrasounds will be analysed. The data retrieved will include gestational age at ultrasound date, fetal abdominal circumference, femur length, head circumference, estimated fetal weight, pulsatility index of umbilical artery, middle cerebral artery, venous duct and uterine artery. * Mothers dietary habits: A semi-quantitative food frequency questionnaire consisting of 86 food items, validated for Portuguese pregnant women, will be applied one week after birth to assess food intake during the second and third trimesters of pregnancy. * Breast milk macronutrient and energy content: The breast milk macronutrient and energy content will be analyzed using the Miris® Human Milk analyzer (Miris AB, Uppsala, Sweden). Mothers will be asked to save circa 4 cc of midfeeding breast milk during the noon feeding, as a systematic sampling of milk collected through 24 hours, in order to minimize daily variability of breast milk composition. Before each use, the analyzer will be calibrated using the standard calibration solution. The breast milk composition will be expressed in densities: Kcal/dL of energy and g/dL of fat, total and true protein, carbohydrates, and ashes. * Neonatal variables: gestational age at birth, sex, parity, birth weight, height and head circumference, gestational age adequacy. * Body composition assessment: Body composition assessment will be conducted using a Displacement Plethysmograph (Pea Pod, Cosmed, Italy), which is validated for newborns. Subsequent assessments will be performed by the same observer at 1 week after discharge, 1 month and 3 months of age (+/- 1 week). The equipment automatically provides fat mass (FM), fat-free mass (FFM) and fat mass percentage (%FM). The same observer will measure length, and this measurement will be used to calculate the fat mass index (FMI). Adiposity will be defined by %FM (FM (kg)/body mass (kg)) and FMI (FM (kg)/length (m²)). Estimate of sample size: Assuming the highest probability (2:1) of reduced adiposity in small-for-gestational-age (SGA) infants with reduced fat-free mass (FFM), SGA infants with reduced adiposity, appropriate-for-gestational-age (AGA) infants with fetal growth deceleration and/or Doppler velocimetry abnormalities with reduced FFM, and AGA infants with fetal growth deceleration and/or Doppler velocimetry abnormalities with reduced adiposity, and considering a 95% confidence interval, the expected sample size is 145 SGA infants and 145 AGA infants. Comparison groups: Body composition will be compared between the following IUGR profiles: SGA infants without fetal growth deceleration or Doppler velocimetry abnormalities; SGA with fetal growth deceleration or Doppler velocimetry abnormalities; AGA with fetal growth deceleration or Doppler velocimetry abnormalities; SGA with reduced FFM (Fat-free-mass); SGA with reduced adiposity; AGA with fetal growth deceleration and/or Doppler velocimetry abnormalities with reduced FFM. AGA with fetal growth deceleration and/or Doppler velocimetry abnormalities with reduced adiposity.

Interventions

DIETARY_SUPPLEMENTSmall for gestational age (SGA) infants

* Body composition assessment will be conducted using a Displacement Plethysmograph (Pea Pod, Cosmed, Italy), which is validated for newborns (Ellis et al., 2007). Subsequent assessments will be performed by the same observer at 1 week after discharge, 1 month and 3 months of age. * At birth and during body composition evaluations, anthropometric measurements (body weight, length and head circumference) will be measured. * The breast milk macronutrient and energy content will be analyzed using the Miris® Human Milk analyzer (Miris AB, Uppsala, Sweden). Mothers will be asked to save, once a week, circa 4 cc of midfeeding breast milk during the noon feeding, as a systematic sampling of milk collected through 24 hours, in order to bring the conditions for expressing milk closer together for all mothers.

DIETARY_SUPPLEMENTAdequate for gestational age (AGA) infants

* Body composition assessment will be conducted using a Displacement Plethysmograph (Pea Pod, Cosmed, Italy), which is validated for newborns (Ellis et al., 2007). Subsequent assessments will be performed by the same observer at 1 week after discharge, 1 month and 3 months of age. * At birth and during body composition evaluations, anthropometric measurements (body weight, length and head circumference) will be measured. * The breast milk macronutrient and energy content will be analyzed using the Miris® Human Milk analyzer (Miris AB, Uppsala, Sweden). Mothers will be asked to save, once a week, circa 4 cc of midfeeding breast milk during the noon feeding, in order to bring the conditions for expressing milk closer together for all mothers.

Sponsors

Centro Hospitalar de Lisboa Central
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
37 Weeks to 41 Weeks
Healthy volunteers
Yes

Inclusion criteria

* IUGR and term GA (37+0/7 to 41+6/7 weeks of gestation)

Exclusion criteria

* Eligible fetuses with congenital malformations * Eligible fetuses with genetic mutations. * Eligible infants with congenital malformations * Eligible intants with inborn errors of metabolism. * Infants who become ill and require hospitalization during the study period * Infants who die during the study period * Parents or legal guardians who do not agree to participate * Parents or legal guardians who abandon the study.

Design outcomes

Primary

MeasureTime frameDescription
Body composition assessment - Fat mass (FM)Fat mass will be assessed 1 week after discharge, 1 month of age and 3 months of ageFat mass will be assessed using air-displacement plethysmography (Pea Pod, Cosmed, Italy) and expressed in kilograms. Unit of measure: Kilograms (kg)
Body composition assessment - Fat-free mass (FFM)Fat-free mass will be assessed 1 week after discharge, 1 month of age and 3 months of ageBody composition will be assessed using air-displacement plethysmography (Pea Pod, Cosmed, Italy) and expressed in kilograms. Unit of measure: Kilograms (kg)
Body composition assessment - Fat mass index (FMI)Fat mass index will be calculated 1 week after discharge, 1 month of age and 3 months of ageFat mass index (FMI) will be calculated by dividing fat mass (kg), obtained from air-displacement plethysmography, by length squared (m²). Formula: FMI (kg/m²) = fat mass (kg) / \[length (m)\]² Unit of Measure: kg/m²
Body composition assessment - Adiposity (%FM)Adiposity will be assessed 1 week after discharge, 1 month of age and 3 months of ageAdiposity will be assessed as fat mass percentage (%FM). Fat mass will be measured using air-displacement plethysmography (Pea Pod, Cosmed, Italy), and adiposity will be calculated as: %FM = \[fat mass (kg) / body weight (kg)\] × 100 Unit of Measure: Percentage (%)

Secondary

MeasureTime frameDescription
Neonatal anthropometry - Body weightAt birth, 1 week after discharge, 1 month of age and 3 months of ageBody weight will be measured using a calibrated neonatal scale. Unit of measure: Kilograms (kg)
Neonatal anthropometry - LengthLength will be measured at birth, 1 week after discharge, 1 month of age and 3 months of ageLength will be measured using an infantometer. Unit of measure: Centimeter (cm)
Neonatal anthropometry - Head circumferenceHead circumference will be measured at birth, 1 week after discharge, 1 month of age and 3 months of ageHead circumference will be measured using a non-stretchable measuring tape. Unit of measure: Centimeter (cm)
Breast milk energy contentWeekly from birth until 3 months of ageEnergy content of breast milk will be measured using the Miris® Human Milk Analyzer (Miris AB, Uppsala, Sweden). Mothers will be asked to save, once a week, circa 4 cc of midfeeding breast milk. Unit of measure: kcal/dL
Breast milk macronutrient concentrationWeekly from birth until 3 months of ageBreast milk macronutrient concentrations, including raw protein, true protein, fat, carbohydrates and ashes will be measured using the Miris® Human Milk Analyzer (Miris AB, Uppsala, Sweden). Mothers will be asked to save, once a week, circa 4 cc of midfeeding breast milk. Unit of measure: g/dL
Mothers dietary habits - Mother energy intakeAssessed once at recruitment, within the first week after birthMaternal dietary intake during the second and third trimesters of pregnancy will be assessed using a semi-quantitative food frequency questionnaire validated for Portuguese pregnant women. Reported frequencies and standard portion sizes will be converted to estimated energy intake. Unit of measure: kcal/day
Maternal dietary habits - Maternal macronutrient intakeAssessed once at recruitment, within the first week after birthMaternal intake of protein, fat, and carbohydrates during the second and third trimesters of pregnancy will be estimated using a semi-quantitative Food Frequency Questionnaire validated for Portuguese pregnant women. Reported food frequencies and portion sizes will be converted into estimated daily macronutrient intake. Unit of measure: g/day
Prenatal fetal biometry and Doppler percentilesAssessed retrospectively during the study periodPrenatal fetal biometry and Doppler measurements will be retrieved from obstetric ultrasound records and recorded as percentiles for gestational age, according to the reference standards used in the clinical ultrasound reports. Parameters will include abdominal circumference, femur length, head circumference, estimated fetal weight, and pulsatility index percentiles for the umbilical artery, middle cerebral artery, ductus venosus, and uterine arteries. Unit of Measure: Percentile
Maternal demographic and clinical variables - Maternal ageAt birth (time of recruitment)Maternal age will be determined from the maternal date of birth recorded in clinical records or reported at recruitment. Unit of Measure: Years
Mother's demographic and clinical variables - Maternal heightAt birth (time of recruitment)Maternal height will be retrieved from clinical records or reported by the mother at recruitment. Unit of Measure: Meters (m)
Mother's demographic and clinical variables - Pre-pregnancy weightAt birth (time of recruitment)Maternal pre-pregnancy weight will be retrieved from clinical records or reported by the mother at recruitment. Unit of Measure: Kilograms (kg)
Mother's demographic and clinical variables - Postpartum weightFrom recruitment until 3 months after birthMaternal postpartum weight will be reported by the mother during follow-up. Unit of Measure: Kilograms (kg)
Mother's demographic and clinical variables - Pregnancy related medical conditionsAssessed retrospectively during the study periodPregnancy-related medical conditions will be retrieved from clinical records, including diabetes mellitus (type 1 or type 2), gestational diabetes, gestational hypertension, pre-eclampsia, chronic renal disease, systemic lupus erythematosus, and anaemia. Unit of Measure: Presence or absence of condition

Countries

Portugal

Contacts

PRINCIPAL_INVESTIGATORManuela Cardoso, RDN, PhD

Unidade Local de Saúde São José

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 3, 2026