NL-OMON24756已完成不适用
The PaPa Trial: Paracetamol as an adjunct to intrapartum Remifentanil/PCA. An RCT of multimodal pain management during labor.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
入选标准
- •In order to be eligible to participate in this study, a subject must meet all of the following criteria:
- •Pregnant, in labour, >3 centimetres dilatation.
- •Pain request during labour, medication of choice: Remifentanil/ PCA.
- •Age 18 years and older.
- •Able to understand the written and verbal information about the PaPa Trial.
排除标准
- •A potential subject who meets any of the following criteria will be excluded from participation in this study:
- •Refusal for participation in the PaPa Trial
- •No adequate communication possible (e.g. language barrier)
- •Use of other opioids, e.g. Pethidine of epidural analgesia <4 hours prior to start of Remifentanil as pain management.
- •Hypersensitivity for Paracetamol.
- •Liver- of kidneydiseases
- •Alcohol abuse
- •Glucose-6-phosphate dehydrogenase
- •Use of other medication that contains Paracetamol
- •Severe nutritional deficiency
研究者
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