TCTR20231008003已完成4 期
EFFECTIVENESS OF EPIDURAL MORPHINE FOR POST- CESAREAN ANALGESIA
适应症
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- CMH
- 入组人数
- 100
研究概览
简要总结
Mean analgesia duration was 3 hrs 56 min in group B no patient in group M required analgesia during first 24 hrs. Respiratory depression was not Observed in any patient in either group. Nausea and Vomiting were significantly less in non morphine group. Pruitis was markedly mainly observed in the morphine group.
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 Years 至 40 Years（—）
- 性别
- Female
入选标准
- •full-term (37-40 weeks)
- •multiparous parturient,
- •age between 18-40 years,
- •scheduled for elective Lower Segment Cesarean Section (LSCS)
排除标准
- •patient's refusal for spinal or epidural anaesthesia,
- •known or suspected dural puncture,
- •body mass index > 30 kg/m2,
- •twin pregnancy,
- •patients with a medical history of hypertension,
- •PIH/ eclampsia,
- •suffering from major pulmonary or cardiovascular disease,
- •thrombocytopenia,
- •allergic to local anaesthetic/ morphine,
- •patients with a history of Obstructive Sleep Apnea.
研究者
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