CTRI/2024/05/066941尚未招募2 期
A prospective randomized comparative study to evaluate efficacy of intrathecal dexamethasone and dexmedetomidine added as adjuvant to bupivacaine in pregnant patient posted for elective LSCS. - NI
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
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
- •ASA Grades 1 & 2
- •BMI 20 TO 30
- •No history of bleeding tendency
- •No previous uterine operation except cesarian section
- •Living foetus
排除标准
- •Patient having systemic disease
- •Severe coronary insufficiency
- •The patient requires repeat intrathecal bupivacaine.
研究者
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