Pain Management Efficiency at Latent Period of Labour
试验速览
- 阶段
- 不适用
- 入组人数
- 150
- 主要终点
- pain score
研究概览
简要总结
Examine the effectiveness of an analgesic in PERFALGAN maternity latent phase of labor.
Examine the safety in PERFALGAN in the mother and the newborn in terms of the level of drug in blood
详细描述
Maternity are latent or first stage of labor and complained of pain at the level of 4 or higher on a scale VAS, and are not in risk (HIGH RISK). And did not receive analgesics within 4 hours.
The sample will consist of at least 100 women in labor.
- women, will be identified in the reception room of a delivery room by midwives.
- The research team will ask for consent after receiving an explanation and confirmation of understanding.
- The midwife will perform and will record pain assessment by visual analog scores .
- Maternity reported pain level 4 and above will be asked four questions out of data collection and offered them treatment I.V. PARACETAMOL 1gr as directed by the physician.
- After giving I.V. PARACETAMOL 1g, carried out and documented estimate of the pain returns (by visual analog scores) after an hour wait at any time to wait four hours and two hours after birth.
In cases of an outbreak of pain can give one of the following:
Option A:
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 55 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •latent phase of labour
排除标准
- •high risk
- •allergy to paracetamol
- •liver insufficiency
研究组 & 干预措施
intervention and data collection
pain management by iv paracetamol
干预措施: iv paracetamol (Drug)
结局指标
主要结局
pain score
时间窗: pain assessmant by vas scale during the latent phase of labor at delivery room. the data will be presented through study completion, an average of 1 year
vas
次要结局
- level of paracetamol(at the end of labor , blood samples from the mother and from the umbelical cord. the data will be presented through study completion, an average of 1 year)
- pain experience(72 hours after labor , the data will be presented through study completion, an average of 1 year)
- pain influences(72 hours after labor, the data will be presented through study completion, an average of 1 year)
- pain experience and analgesia(72 hours after labor, the data will be presented through study completion, an average of 1 year)
研究者
Oleg Shnaider
head of delivery room
Western Galilee Hospital-Nahariya