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临床试验/NCT06642818
NCT06642818尚未招募不适用

Evaluation of the Effectiveness of PREVENIR (PREVention ENvIronnement Reproduction) Platforms on Urinary Markers of Chemical Exposures - Unblinded Randomized Clinical Trial. PREVENIR-G

University Hospital, Bordeaux0 个研究点目标入组 300 人开始时间: 2025年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
300
主要终点
Urinary phenoxyacetic acid concentration

研究概览

简要总结

Unblinded randomized clinical superiority trial in two parallel groups (intervention vs. no intervention) national multicentre to evaluate the effectiveness of the platforms on the evolution of phenoxyacetic acid levels measured in the urine at inclusion and 3 months after the intervention for patients who received the intervention compared to patients who did not receive the intervention.

详细描述

it is now recognized that there is a link between certain environmental exposures (occupational and extra-occupational) and reproductive pathologies. During pregnancy, environmental exposures are associated with an increased risk of spontaneous miscarriage, congenital malformations, certain adverse outcomes (fetal death in utero, intrauterine growth retardation, prematurity) and could also increase the risk of chronic disease in childhood and adulthood (hypothesis of developmental origins of health and disease), and have transgenerational effects. Intervention studies have shown efficacy in reducing exposures to certain chemicals, particularly by reducing exposure to cosmetics. In the scientific literature, a pre-conception visit is recommended to identify environmental exposures. In France, platforms are dedicated to the evaluation of environmental exposures in patients with fertility disorders and pregnancy-related pathologies and provide support for the implementation of targeted prevention actions.

The intervention is taken care of by the PREVENIR platforms. This care consists of a consultation carried out by an environmental health expert (midwife, environmental health engineer) from the PREVENIR platforms. This consultation is carried out through a protocolized interview already developed which allows the identification of exposure to risk factors on reproduction. During the interview, prevention messages targeted at the exposures identified during the interview are delivered.

研究设计

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

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • All pregnant women less than 24 SA of age referred to the PREVENIR platforms participating in the study for management.
  • Only women less than 24 SA months pregnant will be included to limit the number of women who gave birth during the study.
  • More than 18 years old
  • For qualitative study:
  • Professionnal working within PREVENIR platforms
  • Women included in the intervention group and who agreed with participating

排除标准

  • Women under court protection, under guardianship or curatorship, severely altered physical and/or psychological health, which, in the opinion of the investigator, may affect the participant's compliance to the study.
  • Women with an altered medical condition related to prgnancy that may required a therapeutic abortion according to the environmental expert
  • Non-French speakers

结局指标

主要结局

Urinary phenoxyacetic acid concentration

时间窗: 3 months

Difference in urinary phenoxyacetic acid concentration between inclusion and 3 months after the intervention. This difference will be compared between the group that received the intervention and the group that did not.

次要结局

  • Urinary levels of pyrethroids(3 months)
  • Occupational exposures characterization(3 months)
  • Chemical exposome(3 month)
  • Endogenous metabolome(3 months)
  • Exhaled CO concentration(3 months)
  • Urinary phenoxyacetic acid concentration(3 months)
  • Transferability of the intervention(5 months)
  • Professionals' perceptions(5 months)
  • Professionals' and patients' appreciation and perceived effectiveness(5 months)
  • Determinants influencing patients' engagement(5 months)
  • Implementation-related factors(5 months)
  • Proportion of individuals exposed to occupational reproductive risk factors(3 months)
  • Urinary levels of parabens(3 months)
  • Urinary levels of phthalates(3 months)
  • Urinary levels of bisphenols(3 months)

研究者

发起方
University Hospital, Bordeaux
申办方类型
Other
责任方
Sponsor

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