To study the correlation of hyponatremia with the fetomaternal outcome in patients of preeclampsia with severe features and to study its association as a marker of the severity of preeclampsia
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- PGIMER
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- 1) Fetomaternal outcome in preeclamptic patients with severe features presenting with hyponatremia
研究概览
简要总结
This study is a prospective observational study to study the correlation of hyponatremia with the fetomaternal outcome in preeclamptic patients with severe features and to study whether hyponatremia is an independent marker for the severity of preeclampsia.Sample size is 100.The primary outcome is to study the correlation of hyponatremia with the fetomaternal outcome in preeclamptic patients with severe features and to study association of hyponatremia as an independent marker for the severity of preeclampsia.The secondary outcome is to study the prevalence of hyponatremia in preeclamptic patients with severe features.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 45.00 Year(s)（—）
- 性别
- Female
入选标准
- •Pregnant women with the period of gestation between 20 to 40 weeks admitted in labour ward with blood pressure more than or equal to 140/90 mmHg measured on 2 occasions 4 hours apart consenting to be enrolled in study.
- •Age more than or equal to 18 years 3)All patients falling under the ACOG Criteria for severe Preeclampsia.
排除标准
- •Pregnant women who do not consent for study 2)Women with chronic kidney disease, liver disease, cardiovascular disease, collagen vascular disease, chronic hypertension, diabetes, neoplasm, with major fetal anomaly, endocrine disorders causing electrolyte imbalance, CNS disorders, on steroids /diuretics.
结局指标
主要结局
1) Fetomaternal outcome in preeclamptic patients with severe features presenting with hyponatremia
时间窗: 1 year
2) Association of hyponatremia with the severity of preeclampsia
时间窗: 1 year
次要结局
- Proportion of hyponatremia in preeclamptic patients with severe features(1 YEAR)