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临床试验/NCT02862496
NCT02862496Unknown不适用

Urine N-telopeptide, Serum Vit D, Parathormone and Calcium Levels in Hyperemesis Gravidarum

Kayseri Education and Research Hospital1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2016年6月最近更新:
适应症

试验速览

阶段
不适用
发起方
入组人数
60
试验地点
1
主要终点
Urine N- telopeptide levels in Pregnant Women with Hyperemesis Gravidarum

研究概览

简要总结

The purpose of the study is to determine whether maternal bone resorption would be seen in Hyperemesis Gravidarum and could be detected in early period using serum vitamin D levels, serum calcium (Ca) levels, serum parathormone (PTH) levels and urine N- telopeptide levels in the patients with Hyperemesis Gravidarum.

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

入选标准

  • weeks of gestation pregnant women in both groups
  • İn hyperemesis group; 5% weight loss with regard to pre-gestation vomiting more than 3 times 3-5 % weight loss with ketonuria.

排除标准

  • Other pathologies that cause nausea and vomiting in pregnancy gastroenteritis gastroparesis gall duct diseases hepatitis peptic ulcers appendicitis pyelonephritis ovarian torsion urinary tract stones diabetic ketoacidosis hyperthyroidism hyperparathyroidism migraine pseudo tumor cerebra vestibular diseases
  • Additionally some situations causing to rise of Ntx levels osteoporosis paget disease bone tumors
  • Furthermore some of conditions resulted in pre-menopausal osteoporosis or decreasing in Bone Mineral Density Malignancy Smoking Celiac Disease Depression Inflammatory Bowel Disease Pre-gestational Diabetes Chronic Kidney or Liver Disease Drug Use such as steroids, anticonvulsants, antiepileptic, heparin or low molecular weight heparin

结局指标

主要结局

Urine N- telopeptide levels in Pregnant Women with Hyperemesis Gravidarum

时间窗: 4 months

Serum Vitamin D Levels in Pregnant Women with Hyperemesis Gravidarum

时间窗: 4 months

Serum Calcium Levels in Pregnant Women with Hyperemesis Gravidarum

时间窗: 4 months

Serum Parathormone Levels in Pregnant Women with Hyperemesis Gravidarum

时间窗: 4 months

次要结局

未报告次要终点

研究者

发起方
Kayseri Education and Research Hospital
申办方类型
Other Gov
责任方
Principal Investigator
主要研究者

Erdem Sahin

Principal Investigator

Kayseri Education and Research Hospital

研究点 (1)

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