跳至主要内容
临床试验/NCT06339567
NCT06339567进行中(未招募)不适用

Evaluation of the Venous Thrombotic Biological Profile of Different PCOS Phenotypes: French Cross-sectional Study

Fondation Hôpital Saint-Joseph1 个研究点 分布在 1 个国家目标入组 352 人开始时间: 2024年2月8日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
进行中(未招募)
入组人数
352
试验地点
1
主要终点
biological procoagulant profile

研究概览

简要总结

Polycystic ovary syndrome (PCOS) is the most common endocrine disorder of women of childbearing age. PCOS can be individualized into several phenotypes, taking into account in particular the presence of hyperandrogenism, insulin resistance and BMI. Hyperandrogenism and insulin resistance appear to be important factors in the development of cardiovascular cardiovascular disease. In addition, patients frequently use anti-androgenic and/or contraceptive treatments contraceptives, such as combined hormonal contraception (CHC), the use of which is associated with an increased cardiovascular and thrombo and venous thrombosis (VTE). A meta-analysis published in 2020 by Gariani et al.

based on three large studies, estimated the risk of VTE in women with PCOS after adjustment for obesity and hormone therapy. This risk was significantly higher compared with women without PCOS (pooled OR 1.89, CI95% 1.60-2.24). No study has looked specifically investigated the risk of VTE according to different PCOS phenotypes. Such data would be very useful in clinical practice, as it would enable monitoring, contraceptive treatment and anti-androgenic anti-androgen treatment according to the PCOS phenotype, while limiting risks. Assessing the differences PCOS phenotypes is limited by the large sample size required. required. VTE is a rare event in women of childbearing age, and the number of PCOS phenotypes is high.

PCOS phenotypes. Intermediate markers of VTE risk are used in these situations. These markers are thrombin generation tests (notably ETP) and their sensitivity to activated protein C (nAPCsr) and thrombomodulin (nTMsr), as well as sex-hormone binding globulin (SHBG).

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 35 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • Be between 18 and 35 years of age at the time of inclusion;
  • Able to give non-opposition
  • Strong suspicion of PCOS according to 2023 recommendations
  • Have stopped hormonal contraception for at least 3 months or insulin-sensitizing treatment for at least 3 months.
  • Fasting for at least 12 hours.
  • Be affiliated to a health insurance scheme.
  • French-speaking

排除标准

  • Already included in a type 1 interventional research protocol (RIPH1).
  • Be under guardianship or curatorship
  • Deprived of liberty
  • Under court protection
  • Pregnant (positive urine or blood pregnancy test), or within 3 months of post-partum or post abortum, or breastfeeding (or within 3 months of weaning)
  • Using hormonal contraception or insulin-sensitizing therapy (a wash-out of at least 3 months before inclusion).
  • Have a personal history of VTE or known thrombophilia.
  • Current anticoagulant or antiaggregant treatment or treatment stopped less than one month before inclusion.
  • Have a severe personal medical history in the previous 6 weeks (fracture, infection, hospitalization, surgery, cardiovascular event, cancer).

研究组 & 干预措施

Thrombotic profil

Other

干预措施: Thrombotic profile (Diagnostic Test)

结局指标

主要结局

biological procoagulant profile

时间窗: one year

Evaluation of the biological procoagulant profile in women of childbearing age with PCOS, in relation to the presence or absence of insulin resistance, by comparing FTE levels between women with PCOS and women without PCOS. the presence or absence of insulin resistance, by comparing ETP levels between women with PCOS without and with insulin resistance

次要结局

  • comparison of procoagulant profile depending on insulin resistance(1 year)
  • comparison of procoagulant profile depending on PCOS phenotype(1 year)
  • comparison of procoagulant profile depending on AMH Rate(1 year)
  • comparison of QoL score depending on PCOS phenotype(1 year)
  • Insuline resistance and weight(1 year)
  • comparison of procoagulant profile depending on hyperangrogenism(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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