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临床试验/NCT07399691
NCT07399691已完成不适用

Effect of Adding Dexamethasone to Bupivacaine in Ultrasound-Guided Supraclavicular Brachial Plexus Blocks Versus Bupivacaine Alone for Upper Limb Orthopaedic Surgery

Arsi University1 个研究点 分布在 1 个国家目标入组 54 人开始时间: 2024年1月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
54
试验地点
1
主要终点
The onset of sensory and motor blockade, and the duration of sensory and motor blockade in minutes.

研究概览

简要总结

  • SCBPBs provides optimal conditions for procedures performed below the mid-upper arm (elbow, forearm, wrist, hand) due to its high success rate and ease of access.
  • Dexamethasone, when administered perineurally as an adjuvant for a supraclavicular block, demonstrated early onset of sensory and motor block, a prolonged duration of sensory and motor block, and a lower number of rescue analgesics as compared to bupivacaine alone.
  • A combination of dexamethasone and bupivacaine is paramount in adult orthopeadic patient to enhance the efficacy of pain management under ultrasound-guided supraclavicular brachial plexus block.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Aged 18-60 years with ASA I and II who were scheduled for elective elbow, forearm, or hand surgery under ultrasound-guided supraclavicular block.

排除标准

  • Patients who refused, used local anaesthetics other than bupivacaine, had multiple traumas, addition of another additive, bleeding disorders, patients diagnosed with chronic pain, cancer pain, local infection at the injection site, history of local anaesthetic allergy, patients with anxiety, and inability to comprehend or use the pain rating scale

研究组 & 干预措施

Group B

Patients received a supraclavicular brachial plexus block with 40 ml of 0.25 % bupivacaine alone.

Group DB

Patients received a supraclavicular brachial plexus block with dexamethasone 2 ml (8 mg) added to 38 ml of 0.25 % bupivacaine.

干预措施: Dexamethasone 8 mg (Drug)

结局指标

主要结局

The onset of sensory and motor blockade, and the duration of sensory and motor blockade in minutes.

时间窗: with in the first 24hrs after procedure

1. The onset of sensory: the period between injecting a study solution and losing sensation to a pinprick at every nerve distribution 2. The onset of motor block: The duration between the injection of the study solution and paresis in every nerve distribution. 3. duration of sensory: the period between the onset of a sensory block and the complete restoration of sensation. 4. Duration of motor block: the period between the onset of a motor block and the complete restoration of motor function.

次要结局

  • postoperative pain score by a visual analogue scale(with in the first 24 hrs after procedure)
  • First analgesic request time(With in the first 24 hrs after surgery)

研究者

发起方
Arsi University
申办方类型
Other
责任方
Principal Investigator
主要研究者

Mohammed Gebi

lecturer at arsi university

Arsi University

研究点 (1)

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