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临床试验/NCT02682004
NCT02682004已完成不适用

Serotonin, Leptin and Adiponectin Level in Patients With Postpartum Depression: Controlled Study

Zeynep Kamil Maternity and Pediatric Research and Training Hospital1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2016年2月最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
400
试验地点
1
主要终点
Blood level (ng/ml) ELİSA

研究概览

简要总结

After vaginal delivery, all of the participants will evaluate by using Edinburg depression scale and venous blood sample will obtain. Postpartum depression will consider the result of scale 13 and above according to Turkhish translate. Then leptin, adiponectin and serotonin level will compare between depressed and nondepressed women.

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

入排标准

年龄范围
20 Years 至 40 Years(Adult)
性别
Female
接受健康志愿者

入选标准

  • All women who gave birth

排除标准

  • women with previously diagnosed depression and any psychiatric disorders
  • women with previously take antidepressan and antipshycothic
  • women giving birth to children with anomalies
  • women with undertake surgery for peripartum hemorrhage

结局指标

主要结局

Blood level (ng/ml) ELİSA

时间窗: 1 month

次要结局

未报告次要终点

研究者

发起方
Zeynep Kamil Maternity and Pediatric Research and Training Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mehmet Baki Senturk

Principal investigator

Zeynep Kamil Maternity and Pediatric Research and Training Hospital

研究点 (1)

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