Comparative analgesic potency of ropivacaine0.2% versus 0.5% with dexmedetomidine as an adjuvant in preincision USG rectus sheath block for midline incision

Shalini Sharma1 个研究点分布在 1 个国家目标入组 60 人开始时间: 2017年8月14日最近更新: 2017年7月8日

试验速览

阶段: 不适用
状态: 尚未招募
发起方: Shalini Sharma
入组人数: 60
试验地点: 1
主要终点: To compare the duration of post op analgesia after giving equal volumes and different concentration of ropivacaine 0.25% and 0.5% with dexmeditomidine 1mcg per kg in USG guided rectus sheath block.

研究概览研究设计入排标准结局指标研究者研究点记录与标识符相似试验

研究概览

简要总结

The present study will be conducted at Dr. Rajendra Prasad Govt. medical college Tanda. The patients with perforated duodenal ulcer posted for emergency surgeries and requiring midline incision will be inducted in the study. These patients will be given rectus sheath block after induction with two different doses of dexmedetomidine in combination with ropivacaine on both sides. Duration of analgesia will be assessed in the post operative period.

研究设计

研究类型: Interventional
分配方式: Computer generated randomization
盲法: Participant, Investigator and Outcome Assessor Blinded

入排标准

年龄范围: 18.00 Year(s) 至 65.00 Year(s)（—）
性别: All

入选标准

•ASA 1 and 2 patients.
•BMI 18.5-39.
•Patients scheduled for emergency laparotomy for duodenal ulcer perforations.

排除标准

•Patient refusal.
•Bleeding and coagulation disorders.
•Local infection at the block site.
•Allergy to study drugs.

结局指标

主要结局

To compare the duration of post op analgesia after giving equal volumes and different concentration of ropivacaine 0.25% and 0.5% with dexmeditomidine 1mcg per kg in USG guided rectus sheath block.

时间窗: Every 30 min till pain starts.

次要结局

Patient satisfaction with pain control.(Number of a rescue analgesic requirement in 24 hours.)

研究者

发起方

Shalini Sharma

申办方类型

Other [self]

研究点 (1)

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