A Comparison of Safety and Effectiveness of Epidural Morphine Versus Epidural Morphine with Dexamethasone for Post Operative Analgesia in Infraumbilical Surgeries
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- To compare the duration of postoperative analgesia between epidural morphine versus combination of epidural morphine with dexamethasone among patients undergoing infraumbilical surgeries
研究概览
简要总结
Epidural morphine provides effective pain relief and patient satisfaction following major surgeries. It acts by binding to opioid receptors in the spinal cord, thereby reducing transmission of pain signals. However adverse effects of opioids such as pruritis, nausea, vomiting, urinary retention are non-fatal but troublesome whereas delayed respiratory depression especially with higher doses of epidural morphine (>2 mg) can be a serious side effect. Dexamethasone is a long-acting corticosteroid improves quality of sensory block in peripheral nerve blocks and epidural anaesthesia. The mechanism of action is by decreasing inflammation, delaying impulses in C-fibers, and stopping the ectopic discharges of the nerves, thus enhances the duration of analgesia with opioid sparing and antiemetic effects. This study has been designed to evaluate the usefulness of 1mg morphine versus combination of 0.5mg morphine and 4mgdexamethasone in providing postoperative analgesia with respect to duration and quality of analgesia.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- Participant and Investigator Blinded
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)(—)
- 性别
- All
入选标准
- •American Society Of Anaesthesiologist grade I and II Patients willing to give informed consent.
排除标准
- •Pregnant women patients with history of long term use of corticosteroids or any analgesics patients with history of allergy to study drugs.
结局指标
主要结局
To compare the duration of postoperative analgesia between epidural morphine versus combination of epidural morphine with dexamethasone among patients undergoing infraumbilical surgeries
时间窗: 24 hours
次要结局
- to compare adverse effects and hemodynamic changes between two groups(24 hours)
研究者
Dr Santhosh M C B
Mandya Institute of Medical Sciences
