跳至主要内容
临床试验/NCT04443660
NCT04443660已完成不适用

Autophagy/Apoptosis Balance During Pregnancy

Centre Hospitalier Universitaire de Nīmes1 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2020年12月30日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
97
试验地点
1
主要终点
Potential autophagy induction activity in all groups

研究概览

简要总结

The object of this study is to assess the intra- and inter-individual variability of apoptosis and autophagy activities in women during pregnancy: 1 / in women with a normal pregnancy and 2 / in pregnant women particularly at risk of complications.

The study investigators hypothesize that there would be an intra-trophoblastic dialogue between the mechanisms of autophagy and apoptosis, the promotion of one partially inhibiting the other. The increase in trophoblastic autophagy during pregnancy could thus constitute an anti-apoptosis defense phenomenon, the exhaustion of which would lead to cellular apoptosis and to pathogenic consequences when it devastates the syncytiotrophoblast.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

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

入选标准

  • Patients followed at the CHU Nimes prior to 33 weeks gestation who give birth at the hospital
  • The patient must have given their free and informed consent and signed the consent form
  • The patient must be a member or beneficiary of a health insurance plan

排除标准

  • The subject is participating in a category 1 interventional study associated with a medication, or is in a period of exclusion determined by a previous study
  • The subject refuses to sign the consent
  • It is impossible to give the subject informed information
  • The patient is under safeguard of justice or state guardianship
  • Multiple pregnancy

结局指标

主要结局

Potential autophagy induction activity in all groups

时间窗: Delivery plus or minus 2 weeks (Month 6)

Microtubule-associated protein 1A/1B-light chain 3 fluorescence ratio

次要结局

  • Autophagy kinetics between groups(Delivery plus or minus 2 weeks (Month 6))
  • Placental Growth Factor in each group(Delivery plus or minus 2 weeks (Month 6))
  • Renal function(Delivery plus or minus 2 weeks (Month 6))
  • Whole blood count(Delivery plus or minus 2 weeks (Month 6))
  • Fibrin levels(Delivery plus or minus 2 weeks (Month 6))
  • Inflammation(Delivery plus or minus 2 weeks (Month 6))
  • Activated partial thromboplastin time(Delivery plus or minus 2 weeks (Month 6))
  • Fibrinogen level(Delivery plus or minus 2 weeks (Month 6))
  • Type of autophagy inhibition per patient in all groups(Delivery plus or minus 2 weeks (Month 6))
  • Apoptosis kinetics between groups(Delivery plus or minus 2 weeks (Month 6))
  • Soluble fms-like tyrosine kinase-1(Delivery plus or minus 2 weeks (Month 6))
  • Acquired thrombophilia(Delivery plus or minus 2 weeks (Month 6))
  • Prothrombin time(Delivery plus or minus 2 weeks (Month 6))
  • Thrombin generation time(Day 0)
  • Potential apoptosis induction activity in all groups(Delivery plus or minus 2 weeks (Month 6))
  • Inter- and intra-individual apoptosis/autophagy ratio in all groups(Delivery plus or minus 2 weeks (Month 6))
  • Constitutive thrombophilia(Day 0)
  • fetal haemoglobin(Delivery plus or minus 2 weeks (Month 6))

研究者

发起方
Centre Hospitalier Universitaire de Nīmes
申办方类型
Other
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验