CTRI/2024/12/078300尚未招募不适用
A study to compare the efficacy of EMLA (Prilox) cream vs placebo application 1 hour prior to IV cannulation on procedural analgesia.
Smt Bhikiben Kanjibhai Shah Medical Institute and Research Cen1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2024年12月30日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- This observational study will help us to assess the efficacy of EMLA
研究概览
简要总结
The purpose of the current study is to compare the efficacy of
EMLA (Prilox) cream to reduce pain while inertion of intravenous cannula in comparison to placebo application 1 hour prior on the basis of visual analog pain scale.
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 18.00 Year(s) 至 60.00 Year(s)（—）
- 性别
- All
入选标准
- •INCLUSION CRITERIA : 1) Patient willing to sign the written & informed consent.
- •Patients posted for elective surgeries.
- •Patients belonging to American Society of anesthesiologists grade I, Il amd III.
排除标准
- •EXCLUSION CRITERIA: 1) Patients with known hypersensitivity to EMLA cream or any other local anesthetics.
- •Patients with methemoglobinemia or on drugs that may cause methemoglobinemia.
- •Patients with mental illness.
- •Patients with open wounds on dorsum of hand.
结局指标
主要结局
This observational study will help us to assess the efficacy of EMLA
时间窗: Baseline | 60 minutes before intravenous cannulation
(PRILOX) cream when compared to placebo application 1 hour prior to iv
时间窗: Baseline | 60 minutes before intravenous cannulation
cannulation.
时间窗: Baseline | 60 minutes before intravenous cannulation
次要结局
- This observational study will help us to assess the reduction in VAS score following application of EMLA((PRILOX) cream v/s placebo application 1 hour prior to iv cannulation.)
研究者
Shah Vihar Pauravbhai
Smt.Bhikiben Kanjibhai Shah Medical Institute and Research Centre
研究点 (1)
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