PACTR202206670556358尚未招募3 期
Study to assess the feasibility, safety, and effectiveness of high-dose oral tramadol and rectal diclofenac in controlling post-caesarian section pain in women admitted at Nkhata Bay district hospital: protocol for a randomized controlled trial
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 入组人数
- 70
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
- 年龄范围
- 19 Year(s) 至 44 Year(s)（—）
- 性别
- Female
入选标准
- •18 years or older, elective or emergency caesarian section
排除标准
- •without pre-eclampsia, intra-operative or obstetric complications such as post-partum hemorrhage (PPH), surgical infections, ASA III or IV, use of general anesthesia, history of peptic ulcer disease, gastric bleeding, recent opioid use (within 30 days), renal or liver disease, chronic pain disorders or those who refuse consent
研究者
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