CTRI/2023/11/059618尚未招募2 期
A comparative study to evaluate efficacy of intrathecal fentanyl and intrathecal midazolam added as adjuvant to Bupivacaine 0.5 (heavy) in patients undergoing LSCs - NI
Acharya Vinobha Bhave Rural Hospital0 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. Age between 18 to 35years
- •2. Patients undergoing cesarean section
- •3. Primi gravida with gestational age more than 37 weeks
- •4. Body mass index 20 to 29.9kg/meter square
- •5. Intact amniotic membrane
- •6. No history of bleeding tendency or coagulopathies or with any neuromuscular disorders or neurological diseases.
- •7. No previous uterine operations except cesarean sections
- •8. Living fetus
- •10. Patients giving informed consent.
排除标准
- •1. Patients who are multigravida, previous LSCS.
- •2. ASA CLASS 3 AND CLASS 4.
- •3. Patients refusal.
- •4. Patients with any co-morbities.
- •5. Patients with infection at the site of injection.
- •6. Patients with sensitivity to local anaesthetic agent, fentanyl and midazolam.
研究者
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