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Идёт набор NCT06083415

Early Breast Growth in Girls Aged 6 to 8 Years in the Current Environmental Context

Без фазы С лечением Puberty, Precocious Breast Environmental Exposure

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Environmental health measures.
Кому может быть актуально
Состояния в реестре: Puberty, Precocious, Breast, Environmental Exposure. Базовые параметры: 6 лет — 8 лет · Женщины.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
Франция
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Early Breast Growth in Girls Aged 6 to 8 Years in the Current Environmental Context: Clinical and Biological Parameters, Level of Impregnation With Endocrine Disruptors and Evaluation of the Impact of Environmental Health Measures

Обзор

Various studies show an increase in the number of cases of early puberty in girls with breast development with a variable clinical presentation and evolution. This increasing phenomenon concerns girls between 6 and 8 years old. In a large number of cases, from 70 to 95% depending on the series, no medical cause is found and environmental factors are suspected to be involved. Descriptive studies of these patients are scarce and not always provide an overview of all the parameters in line with the concept of the exposome. The PENELOPE clinical trial will allow to analyze a large number of parameters, including the adipose tissue, its metabolism, the endocrine disruptors, and the epigenetic modifications, and to study the impact of environmental health measures in the evolution of these parameters. The data from the analyses of the endocrine disruptors of the patients will be explored in parallel in experimental models (amphibians, murine, cellular) in order to test potential mechanistic hypotheses.

Вмешательства

  • Другое Environmental health measures
    MRI will be used to confirm the presence of breast buds, to measure the size of the ovaries and uterus, as well as the fraction of fat mass (abdominal, subcutaneous, liver and bone marrow). The bood and urine tests will allow to measure different biological and metabolic parameters. The presence of endocrine disruptors will be determined in the hair. The bone age x ray will be estimate the maturity of the child's skeletal system. Photographs of the teeth will also be taken to be studied by pedia

Первичные конечные точки

  • Change from baseline of the size of the breast development measured by Magnetic Resonance Imaging [Срок оценки: Baseline, 3 months]
  • Change from baseline of the size of ovaries/uterus measured by Magnetic Resonance Imaging [Срок оценки: Baseline, 3 months,]
  • Change from baseline of the abdominal fat surface measured by Magnetic Resonance Imaging [Срок оценки: Baseline, 3 months]
  • Change from baseline of the weight [Срок оценки: Baseline, 3 months, 6 months]
  • Change from baseline of the height [Срок оценки: Baseline, 3 months, 6 months]
  • Body mass index (BMI) [Срок оценки: Baseline, 3 months, 6 months]
Вторичные конечные точки (12)
  • Measurement of endocrine disruptors in hair [Срок оценки: Change from baseline at 90 days]
  • Tanner scale [Срок оценки: Change from baseline at 90 and 180 days]
  • Bone age determination by X ray [Срок оценки: Change from baseline at 90]
  • Degree of severity of teeth hypomineralisation [Срок оценки: Baseline, 3 months]
  • Follicle-stimulating hormone (FSH) level [Срок оценки: Change from baseline at 90 days and 180 days]
  • Estradiol (E2) level [Срок оценки: Change from baseline at 90 days and 180 days]
  • Testosterone Level [Срок оценки: Change from baseline at 90 days and 180 days]
  • 17 hydroxyprogesterone level [Срок оценки: Change from baseline at 90 days and 180 days]
  • Dehydroepiandrosterone sulfate level [Срок оценки: Change from baseline at 90 days and 180 days]
  • Sex Hormone-Binding Globulin level [Срок оценки: Change from baseline at 90 days and 180 days]
  • Thyroid Stimulating Hormone level [Срок оценки: Change from baseline at 90 days and 180 days]
  • FT4 (Free Thyroxine hormone) level [Срок оценки: Change from baseline at 90 days and 180 days]

Критерии участия

For patients:

Критерии включения

  • Girls aged 6 to 8 years
  • Presenting a breast development (isolated or not)
  • Undergoing scheduled pediatric day hospital care (HDJ)
  • Who agree to participate in the study
  • Whose parents agree to their child's participation in the study
  • French speaking
  • Whose parents speak French
  • Affiliated to social security

Критерии исключения

  • Organic brain causes of precocious puberty: History of neurocerebral disease (malformations, developmental abnormalities)
  • Organic causes of precocious puberty: Mac Cune Albright syndrome, ovarian cyst or tumor and adrenal hyperplasia
  • History of chemotherapy or radiation therapy
  • Presenting with a communication disorder
  • Pregnancy
  • Persons under protective measures
  • Persons deprived of liberty for judicial or administrative reasons

For controls:

Критерии включения

  • Girls aged 6 to 8
  • Tanner stage 1: Absence of breasts and hairiness
  • Coming for routine consultation in the pediatric HDJ at Saint-Vincent-de-Paul hospital, or at the BLM practice in Lambersart, or to radiology for an MRI for another medical other medical reason
  • Agree to participate in the study
  • Whose parents agree to their child's participation in the the study
  • French-speaking
  • Whose parents speak French
  • Affiliated with social security

Критерии исключения

  • Signs of puberty (Tanner stages 2, 3, 4 and 5 for breast development) breast development)
  • Previous chemotherapy or radiotherapy
  • Presenting a communication disorder
  • Pregnant women
  • Persons under protective supervision
  • Persons deprived of their liberty for judicial or administrative reasons

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Нерандомизированное
Модель
Одна группа
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

Франция · 2 центра
  • Cabinet BLM — Lambersart
  • Saint Vincent hospital — Lille

Идентификаторы

NCT: NCT06083415 · RT-17

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗