IRCT20221109056455N1招募中3 期
A prospective randomized controlled study comparing 0.75% hyperbaric ropivacaine with 0.5% hyperbaric bupivacaine in spinal anesthesia for elective caesarean delivery
Tata Main Hospital, Jamshedpur0 个研究点目标入组 98 人开始时间: 待定最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 98
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
- 18 years 至 no limit（—）
- 性别
- Female
入选标准
- •ASA physical status 1 and 2
- •Pregnant adults for elective caesarean section
排除标准
- •Allergy to Ropivacaine or Bupivacaine
- •Infection at the site for spinal anaesthesia
- •Patient with evidence of foetal distress
- •Short stature (150 cm)
- •Tall stature (>180 cm)
- •Obesity(BMI>30)
- •Patient with an obstetrical complication (multiple gestations, bleeding, gestational hypertensive diseases)
- •Psychiatric or seizure disorder
- •Bleeding disorder
- •Cardiac disease
研究者
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