IRCT20230920059483N1已完成2 期
Comparison between neostigmine and atropine added to standard post-dural puncture headache regimen versus standard regimen alone
Combined Military Hospital Kharian, Pakistan0 个研究点目标入组 130 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 发起方
- 入组人数
- 130
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
- 25 years 至 35 years（—）
- 性别
- Female
入选标准
- •Included all patients with post-dural puncture headache diagnosed according to the International Headache Society Criteria, presenting to the anesthesia clinic 48-72 hours after caesarian delivery.
排除标准
- •Patients unwilling for IV or oral therapy
- •Refusal to be included in the study
- •Patients with allergy to either atropine, neostigmine, paracetamol and/or ibuprofen
- •Patients with known history of migraine, cluster headache, patients on anti-depressants
- •Patients with any neurological disease and patients with major respiratory and cardiac disease.
研究者
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