跳至主要内容
临床试验/NCT07471373
NCT07471373招募中不适用

Pesticides and Infertility: Oxidative Stress Via Circulating Cell-free DNA and Gut/Genital Microbiome Signatures in Women With Endometriosis

Centre Hospitalier Universitaire, Amiens1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2026年2月27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
入组人数
160
试验地点
1
主要终点
quantification of circulating free DNA (cfDNA) between both groups

研究概览

简要总结

This project PestiEndoMicro aims to provide an innovative approach, studying endometriosis under the genital and gut microbiota scope. To realize this project, the investigators are planning to dose cfDNA to assess the oxidative stress caused by endometriosis and study its epigenetics. At the same time, the investigators will take a pragmatic approach by assessing pesticide exposure in these patients and estimate the correlation between gut or genital dysbiosis and chemical agent exposure. Also, the investigators will take the initiative to use classic culture, qPCR techniques, and NGS to establish signatures in vaginal, endometrial and gut microbiota in patients with endometriosis. With these approaches, the goal is to gain more knowledge about endometriosis and optimize early diagnosis by establishing a signature in the genital and gut microbiota, but also by dosing the cfDNA. By doing so the investigators could open new opportunities to develop new therapeutic strategies for endometriosis.

研究设计

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

入排标准

年龄范围
18 Years 至 43 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • The "case" group will include:
  • All women aged 18 to 43, with confirmed endometriosis and endometriosis grade 3 or 4 as defined by the 1985 revised version of the American Society of Reproductive Medicine.
  • The "control" group will include:
  • All women aged between 18 and 43, whose infertility problem is proven male infertility and who do not have endometriosis identified by biological, genetic and clinical tests.
  • The following criteria will apply to both groups:
  • All women who have not received antibiotic treatment in the three months preceding inclusion and who are not participating in any pharmacological study.
  • All women who are covered under the national social security health insurance scheme.
  • All women who have signed a written informed consent form, thereby confirming their participation in the study after a period of free and informed reflection.

排除标准

  • All women aged 44 and over.
  • Women who are overweight, obese or anorexic.
  • Women taking antibiotics 3 months prior to inclusion, or participating in a drug study.
  • All women under anti-GnRH treatment, pregnant or suffering from a chronic inflammatory disease such as Crohn's disease, polycystic ovary syndrome, etc.
  • All women whose endometriosis has not been formally confirmed by the tests offered by the Reproductive Medicine and Biology Department, CECOS de Picardie, CHU Amiens-Picardie.
  • All patients under guardianship, curators or safeguard of justice.
  • All patients who have not signed the written consent confirming their participation in the study, after a period of free and informed reflection.
  • Any patient who withdraws her consent for participation in the study.

研究组 & 干预措施

Control group

Active Comparator

The "control" group will include:

All women aged between 18 and 43, whose infertility problem is proven male infertility and who do not have endometriosis identified by biological, genetic and clinical tests.

干预措施: Exposure to endocrine disruptors analysis (Biological)

Case group

Experimental

The "case" group will include: Etude : PestiEndoMic. All women aged 18 to 43, with confirmed endometriosis and endometriosis grade 3 or 4 as defined by the 1985 revised version of the American Society of Reproductive Medicine.

干预措施: Circulating DNA analysis (Biological)

Case group

Experimental

The "case" group will include: Etude : PestiEndoMic. All women aged 18 to 43, with confirmed endometriosis and endometriosis grade 3 or 4 as defined by the 1985 revised version of the American Society of Reproductive Medicine.

干预措施: Vaginal microbiota analysis (Biological)

Case group

Experimental

The "case" group will include: Etude : PestiEndoMic. All women aged 18 to 43, with confirmed endometriosis and endometriosis grade 3 or 4 as defined by the 1985 revised version of the American Society of Reproductive Medicine.

干预措施: Endometrial microbiota analysis (Biological)

Case group

Experimental

The "case" group will include: Etude : PestiEndoMic. All women aged 18 to 43, with confirmed endometriosis and endometriosis grade 3 or 4 as defined by the 1985 revised version of the American Society of Reproductive Medicine.

干预措施: Intestinal microbiota analysis (Biological)

Case group

Experimental

The "case" group will include: Etude : PestiEndoMic. All women aged 18 to 43, with confirmed endometriosis and endometriosis grade 3 or 4 as defined by the 1985 revised version of the American Society of Reproductive Medicine.

干预措施: Exposure to endocrine disruptors analysis (Biological)

Control group

Active Comparator

The "control" group will include:

All women aged between 18 and 43, whose infertility problem is proven male infertility and who do not have endometriosis identified by biological, genetic and clinical tests.

干预措施: Circulating DNA analysis (Biological)

Control group

Active Comparator

The "control" group will include:

All women aged between 18 and 43, whose infertility problem is proven male infertility and who do not have endometriosis identified by biological, genetic and clinical tests.

干预措施: Vaginal microbiota analysis (Biological)

Control group

Active Comparator

The "control" group will include:

All women aged between 18 and 43, whose infertility problem is proven male infertility and who do not have endometriosis identified by biological, genetic and clinical tests.

干预措施: Endometrial microbiota analysis (Biological)

Control group

Active Comparator

The "control" group will include:

All women aged between 18 and 43, whose infertility problem is proven male infertility and who do not have endometriosis identified by biological, genetic and clinical tests.

干预措施: Intestinal microbiota analysis (Biological)

结局指标

主要结局

quantification of circulating free DNA (cfDNA) between both groups

时间窗: 2 years

The primary outcome will be the evaluation of oxidative stress by quantification of circulating free DNA (cfDNA) between patients in the control group and patients with endometriosis and will be established in ng/mL of plasma.

次要结局

  • Variation of Vaginal microbiota signature between both groups(2 years)
  • variation of Endometrial microbiota signature between both groups(2 years)
  • variation of Endocrine disruptors exposure between both groups(2 years)
  • variation of DNA methylation analysis(2 years)
  • variation of Intestinal microbiota signature between both groups(2 years)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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