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临床试验/CTRI/2024/04/065274
CTRI/2024/04/065274尚未招募3 期

Analyzing the efficacy of chest block in comparison with intravenous analgesia for acute pain management in closed chest trauma with a Numeric rating scale (NRS) score of 7 or more, presenting to the Emergency department - A Prospective Pragmatic Interventional study.

Christian Medical College Internal Fluid Research Grant1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2024年5月1日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
Reduction in pain score

研究概览

简要总结

Patients who present to the emergency department (ED) with blunt thoracic trauma are usually managed  with intravenous analgesia including NSAIDS and opioids. Rib fractures are extremely painful and can lead to poor respiratory effort and hypoxia from thoracic splinting. Opioid and non-opioid analgesia often do not provide sufficient or consistent analgesia and may require doses where the adverse effects are more compared to the benefits especially in the elderly population or those with comorbidities such as obesity or reactive airway disease. Many patients in our ED receive a chest block which seems to provide sufficient and long lasting analgesia. Since the blocks are administered by only a few trained personnel in the department presently, many patients do not receive the blocks. In our study we wish to compare the analgesia and improvement in respiratory function between patients who receive a block and those who receive the standard analgesic management.. The analgesia achieved will be objectively scored by the numerical rating scale or visual analogue scale. Improvement in the respiratory function will be assessed with the change in tidal volumes on incentive spirometry. We will also look at success rates of performing these blocks in the emergency department setting by consultants trained to administer the blocks, as well as the average duration of action of the block.

研究设计

研究类型
Interventional
分配方式
Na
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 99.00 Year(s)(—)
性别
All

入选标准

  • All adult patients with blunt thoracic traumas with 2 or more radiologically confirmed rib fractures.

排除标准

  • Patient does not give consent.
  • Open chest wounds.
  • Polytraumatised patients
  • Patients who are haemodynamically unstable or require ICU care
  • Allergy or contraindications to NSAIDs/Paracetamol/Local anaesthetics
  • Pregnant women.

结局指标

主要结局

Reduction in pain score

时间窗: Reduction in pain score from 7 to less than 4, or by more than 50% from time of patient admission in the emergency department till discharge from emergency department, or till 12 hours in the ward.

次要结局

  • 1.Success rate of the block in reducing the pain score(2.Compraison of patient satisfaction.)

研究者

发起方
Christian Medical College Internal Fluid Research Grant
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Gokul Prakash

Christian Medical College and Hospital

研究点 (1)

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