CTRI/2020/08/027280尚未招募2 期
A study to evaluate the duration of post operative analgesia using nalbuphine or butorphanol as adjuvant to intrathecal 0.5% bupivacaine compared to 0.5% bupivacaine alone in lower segmemt cesarean section
SGRDIMSAR0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
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
入选标准
- •1.Patients who are willing to undergo the study.
- •2.Patients undergoing elective LSCS
- •3.Patients American Society of Anesthesiology (ASA) Grade II
排除标准
- •1.Patient refusal
- •2.Patient with Cardiorespiratory problems
- •3.Patient with Coagulopathy
- •4.Patient with Neurological disease
- •5.Patient with Psychological disease
- •6.Patient with Endocrine disease and allergy to used drugs
- •7.Contraindication to drugs.
- •8.Complicated pregnancy.
研究者
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