A Randomised Controlled Trial On Effect Of Acupressure On Nausea And Vomiting In Women With Hyperemesis Gravidarum
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 90
- 试验地点
- 2
- 主要终点
- Degree of nausea and vomiting
研究概览
简要总结
To examine the degree of nausea, vomiting between the acupressure and control group in women with hyperemesis gravidarum
详细描述
A prospective RCT conducted at Department of Obst and Gynae, UKMMC. All pregnant women with a normal intrauterine pregnancy of ≤ 16 week gestation with hyperemesis gravidarum will be assessed by the medical officer/ specialist/ consultant in charge. Explanation regarding the research study will be given for patients who fulfill the inclusion and exclusion criteria. Patients who have understood the research study and consented will be recruited as subjects for the study.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Prevention
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 50 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Onset of vomiting before 16 weeks
- •Vomiting at least 2 times per day
- •Ketonuria on admission
- •Mid stream urine specimen that did not indicate infection
排除标准
- •Non viable pregnancy
- •Molar pregnancy
- •Overt clinical features of thyrotoxicosis
- •Known case of medical illness that associated with nausea and vomiting
- •Patient refusal or patients who are not able to give consent
结局指标
主要结局
Degree of nausea and vomiting
时间窗: day 1 to day 3
measure the effect of acupressure using modified Pregnancy Unique Quantification of Emesis and Nausea (PUQE)
次要结局
未报告次要终点