NCT04747171Unknown不适用
A Comparative Study of Postoperative Analgesia of Different Intrathecal Additives for Spinal Anaesthesia in Elective Caesarean Sections
适应症
干预措施
相关药物
试验速览
- 阶段
- 不适用
- 入组人数
- 105
- 主要终点
- analgesic effect
研究概览
简要总结
we designed this randomized, single -blind, prospective clinical study to test postoperative analgesia of three intrathecal additives in elective caesarean sections which are magnesium, dexamethasone and dexmedetomidine.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- Single (Participant)
入排标准
- 年龄范围
- 18 Years 至 40 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •American Society of Anesthesiologists classII-III adult female patient (age :18 -40 years old )
- •Elective cesarean section under spinal anaesthesia
- •Gestational age > 37 weeks
- •BMI less than 30 kg/m2
排除标准
- •Patient refusal
- •unable to give consent
- •age < 18 or > 40
- •BMI more than 30 kg/m2
- •known allergy to the study medication
- •coagulopathies or on anticoagulant medications
- •diabetic neuropathy
- •patients with psychiatric disorders
研究组 & 干预措施
magnesium intrathecal
Active Comparator
干预措施: intrathecal Magnesium (Drug)
dexamethasone intrathecal
Active Comparator
干预措施: intrathecal dexamthasone (Drug)
dexmedetomidine intrathecal
Active Comparator
干预措施: intrathecal dexmedetomidine (Drug)
结局指标
主要结局
analgesic effect
时间窗: Up to 24 hours after surgery
duration of sensory block
次要结局
未报告次要终点
研究者
Baher Said Elshahat Mohamed Abdelhady
Principal Investigator
Benha University
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