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临床试验/NCT06083415
NCT06083415招募中不适用

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

Lille Catholic University4 个研究点 分布在 1 个国家目标入组 62 人开始时间: 2023年5月15日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
62
试验地点
4
主要终点
Change from baseline of the height

研究概览

简要总结

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.

研究设计

研究类型
Interventional
分配方式
Non Randomized
干预模型
Single Group
主要目的
Prevention
盲法
None

入排标准

年龄范围
6 Years 至 8 Years(Child)
性别
Female
接受健康志愿者

入选标准

  • For patients:
  • Inclusion Criteria:
  • 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

排除标准

  • 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:
  • Inclusion Criteria:
  • 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
  • Exclusion Criteria:
  • 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

研究组 & 干预措施

6 to 8 years old girls, presenting with a breast flare-up

Experimental

Girls aged 6 to 8 years old with breast flare (isolated or not) and scheduled for pediatric day hospital stay

干预措施: Environmental health measures (Other)

6 to 8 years old girls controls

No Intervention

Girls aged 6 to 8 years old controls, scheduled for pediatric day hospital stay, or an office consultation, or an MRI in radiology

结局指标

主要结局

Change from baseline of the height

时间窗: Baseline, 3 months, 6 months

This parameter will allow to describe the clinical evolution of the height after application of environmental health measures

Change from baseline of the size of the breast development measured by Magnetic Resonance Imaging

时间窗: Baseline, 3 months

This parameter will allow to describe the clinical evolution of breast development after application of environmental health measures

Change from baseline of the size of ovaries/uterus measured by Magnetic Resonance Imaging

时间窗: Baseline, 3 months,

This parameter will allow to describe the clinical evolution of ovaries and uterus after application of environmental health measures

Body mass index (BMI)

时间窗: Baseline, 3 months, 6 months

This parameter will allow to describe the clinical evolution of the BMI after application of environmental health measures

Change from baseline of the abdominal fat surface measured by Magnetic Resonance Imaging

时间窗: Baseline, 3 months

This parameter will allow to describe the clinical evolution of the abdominal fat surface after application of environmental health measures

Change from baseline of the weight

时间窗: Baseline, 3 months, 6 months

This parameter will allow to describe the clinical evolution of the weight after application of environmental health measures

次要结局

  • Thyroid Stimulating Hormone level(Change from baseline at 90 days and 180 days)
  • FT4 (Free Thyroxine hormone) level(Change from baseline at 90 days and 180 days)
  • Degree of severity of teeth hypomineralisation(Baseline, 3 months)
  • 17 hydroxyprogesterone level(Change from baseline at 90 days and 180 days)
  • Sex Hormone-Binding Globulin level(Change from baseline at 90 days and 180 days)
  • Bone age determination by X ray(Change from baseline at 90)
  • Tanner scale(Change from baseline at 90 and 180 days)
  • Estradiol (E2) level(Change from baseline at 90 days and 180 days)
  • Measurement of endocrine disruptors in hair(Change from baseline at 90 days)
  • Glycated hemoglobin (HbA1C) level(Change from baseline at 90 days and 180 days)
  • Glycemia level(Change from baseline at 90 days and 180 days)
  • Insulin-like Growth Factor-1 level(Change from baseline at 90 days and 180 days)
  • Follicle-stimulating hormone (FSH) level(Change from baseline at 90 days and 180 days)
  • Testosterone Level(Change from baseline at 90 days and 180 days)
  • Dehydroepiandrosterone sulfate level(Change from baseline at 90 days and 180 days)
  • Androstenedione level(Change from baseline at 90 days and 180 days)
  • Leptine level(Change from baseline at 90 days and 180 days)
  • Luteinizing hormone (LH) level(Change from baseline at 90 days and 180 days)
  • Insulin level(Change from baseline at 90 days and 180 days)

研究者

发起方
Lille Catholic University
申办方类型
Other
责任方
Sponsor

研究点 (4)

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