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临床试验/CTRI/2024/01/061787
CTRI/2024/01/061787尚未招募2/3 期

A COMPARATIVE STUDY OF ULTRASOUND GUIDED SUPRACLAVICULAR AND INFRACLAVICULAR BRACHIAL PLEXUS BLOCK FOR UPPER LIMB ORTHOPEDIC SURGERY

jawaharlal nehru medical college ajmer1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年2月1日最近更新:

试验速览

阶段
2/3 期
状态
尚未招募
入组人数
50
试验地点
1
主要终点
1. Sensory block onset time

研究概览

简要总结

With due approval from institutional ethical committee, a prospective, hospital based, single blinded, randomized controlled study has been planned on  adult patients of either sex.

Study participants will be the patients coming to the orthopedic department planned for upper limb surgeries and listed in the operation theatre in the Department of Anaesthesiology, Jawaharlal Nehru Medical College, Ajmer. A written informed consent will be obtained from all the patients for performance of block after complete explanation about the study protocol, anaesthetic technique, merits and demerits of the procedure and perioperative course of anaesthesia.A comparative study of ultrasound guided supraclavicular and infraclavicular approach of brachial plexus block will be done and sensory block onset will be compared in both the approaches along with other outcome measurements as mentioned in above texts.

研究设计

研究类型
Interventional
分配方式
Coin toss, Lottery, toss of dice, shuffling cards etc
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 90.00 Year(s)(—)
性别
All

入选标准

  • 1 Age group above 18 years.
  • 2 Patients belonging to ASA (American Society of Anaesthesiologists) class-I and II.

排除标准

  • 1 Patients not willing to participate in the study and not giving consent.
  • 2 Uncooperative patients.
  • 3 Patient with chronic pain or on long-term analgesics.
  • 4 Any known hypersensitivity or contraindication to bupivacaine or any other local anesthetic.
  • 5 Local pathology at the site of injection or disability limiting the performance of block.
  • 6 Patients with coagulopathies and bleeding diathesis 7 Neurological diseases or pre existing nerve palsies 8 Inadequate block necessitating institution of general anaesthesia for continuation of surgical procedure.

结局指标

主要结局

1. Sensory block onset time

时间窗: to be assesed by grading points using 3 point scale by pinprick test just after giving the drug in intervals of half min till effect comes

次要结局

  • 1) Time to perform the block

研究者

申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Pooja Mathur

Jawaharlal Nehru Medical College,Ajmer

研究点 (1)

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