跳至主要内容
临床试验/CTRI/2025/03/082268
CTRI/2025/03/082268尚未招募不适用

Effects of local application of common salt on scorpion bite reaction among clients in selected hospitals and selected community in West Bengal.

Soma Patra10 个研究点 分布在 1 个国家目标入组 500 人开始时间: 2025年3月24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
500
试验地点
10
主要终点
1. Reduction in Pain Intensity The study will measure the reduction in pain intensity at the bite site, as assessed by the WHO numerical pain scale at 30 minutes, 1 hour, and 1.30 hours and 6 hours after the application of salt.

研究概览

简要总结

This study is a cluster randomized control multicentre trial comparison efficacy of local application of common salt with standard medical treatment following 500 scorpion bite patients in 10 hospitals of rural areas in West Bengal , India. The primary outcome measure will be reduced  the pain intensity , local swelling and local redness at 30 min, 60 min, 90 min and 06 hours of post intervention following baseline.The secondary outcome measures will consider the time to onset of pain relief and duration of pain relief.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

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

入选标准

  • Patients who will attend within 4 hrs.
  • Patients with hemodynamically stable.

排除标准

  • Patient who are not sure about biting.
  • Patients of unknown bite.
  • Patients who use any therapy used before to reduce pain.
  • Patients with anaphylaxis shock.
  • Patients with severe urticaria.

结局指标

主要结局

1. Reduction in Pain Intensity The study will measure the reduction in pain intensity at the bite site, as assessed by the WHO numerical pain scale at 30 minutes, 1 hour, and 1.30 hours and 6 hours after the application of salt.

时间窗: Base line, pre intervention (o1) | 30 min. post intervention (o2) | 60 min. post intervention (o3) | 90 min. post intervention (o4) | 06 hrs. post intervention (o5)

2. Decrease in Swelling and Inflammation

时间窗: Base line, pre intervention (o1) | 30 min. post intervention (o2) | 60 min. post intervention (o3) | 90 min. post intervention (o4) | 06 hrs. post intervention (o5)

The study will evaluate the decrease in swelling and inflammation at the bite site, as measured by the circumference of the affected limb, at 30 minutes, 1 hour, and 1.30 hours and 6 hours after the application of salt.

时间窗: Base line, pre intervention (o1) | 30 min. post intervention (o2) | 60 min. post intervention (o3) | 90 min. post intervention (o4) | 06 hrs. post intervention (o5)

次要结局

  • 1. Time to Onset of Pain Relief(The study will record the time taken for the patient to experience pain relief after the application of salt.)

研究者

发起方
Soma Patra
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

SOMA PATRA

Govt. College of Nursing ID & BG Hospital Campus

研究点 (10)

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