PACTR202203682996126招募中4 期
The role of Intrathecal Neostigmine as an Adjuvant to Bupivacaine in Ameliorating Post-Dural Puncture Headache for Elective Caesarian Section: A Prospective Randomized Controlled Clinical Trial
Alexandria University Hospital0 个研究点目标入组 722 人开始时间: 2022年3月15日最近更新:
适应症
试验速览
- 阶段
- 4 期
- 状态
- 招募中
- 发起方
- 入组人数
- 722
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
- •American society association (ASA) physical status class II parturients with a single fetus who will be scheduled for an elective caesarian section by Intrathecal block.
排除标准
- •Body mass index more than or equal to 35 kg/m2.
- •Any contraindication to Intrathecal blocks such as local infection, bleeding disorders, or parturient refusal.
- •Allergy to neostigmine or other drugs will be used in the study.
- •Long-term opioid use.
- •A history of chronic pain, migraine, cluster headache.
- •Digestive problems with nausea and vomiting; cognitive dysfunction or memory disorders.
- •Significant renal, hepatic, and cardiovascular diseases.
- •History of urinary retention or bronchial asthma.
- •Inadequate or failed Intrathecal block.
- •Complicated pregnancy such as hypertensive disorders of the pregnancy, abnormal placenta, or uterine atony.
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