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临床试验/NCT04398589
NCT04398589已完成4 期

The Effect of Dexmedetomidine for Suprascapular Nerve Block With Axillary Nerve Block on Plasma Cortisol and Pain-related Cytokines After Arthroscopic Rotator Cuff Repair: a Randomized Controlled Trial

Chuncheon Sacred Heart Hospital1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2015年5月20日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
46
试验地点
1
主要终点
visual analog scale of pain

研究概览

简要总结

Suprascapular nerve block (SSNB) is most commonly used for relieving postoperative pain of arthroscopic rotator cuff repair and it can be used in combination with axillary nerve block (ANB). Dexmedetomidine (DEX) is known as a type of alpha agonist which can elongate the duration of regional block. The aim of this study was to compare the results of dexmedetomidine combined with SSNB and ANB with SSNB and ANB alone on postoperative pain, satisfaction, and pain-related cytokines within the first 48 hours after arthroscopic rotator cuff repair.

Forty patients with rotator cuff tears who had undergone arthroscopic rotator cuff repair were enrolled in this single center, double-blinded randomized controlled trial study. Twenty patients were randomly allocated to group 1 and received ultrasound-guided SSNB and ANB using each mixture of 0.5 ml (50 μg) of DEX and 9.5 ml of 0.75% ropivacaine preemptively. The other 20 patients were allocated to group 2 and underwent ultrasound-guided SSNB and ANB alone using a mixture of 0.5 ml of normal saline and 9.5 ml of ropivacaine. The visual analog scale (VAS) for pain and patient satisfaction (SAT) scores were checked within 48 h postoperatively. The plasma interleukin (IL)-6, -8,-1β, cortisol, and serotonin levels were also measured within 48 h postoperatively.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
20 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • defined rotator cuff tear on preoperative MRI, which indicated repair
  • acceptable arthroscopic surgery, including rotator cuff repair
  • patients >20 years old
  • acceptable routine regional blocks and patient-controlled analgesia (PCA)

排除标准

  • did not undergo arthroscopic rotator cuff repair
  • stopped PCA before 48 h postoperatively due to side effects
  • had a concomitant operation for a Bankart lesion
  • had a history of shoulder operation or fracture
  • had a concomitant neurological disorder around the shoulder
  • underwent conversion to open surgery from the arthroscopy
  • had contraindications for the routine regional blocks used in this study
  • had an known allergy or hypersensitivity against ropivacaine or dexmedetomidine, including other amino-amide local anesthetics or α2-adrenoceptor agonists.

研究组 & 干预措施

SSNB and ANB c DEX

Experimental

We used 9.5 ml of 0.75% ropivacaine and 0.5 ml (50 μg) of dexmedetomidine each for SSNB and ANB.

干预措施: Dexmedetomidine injection (Drug)

SSNB and ANB c saline

Placebo Comparator

We used 9.5 ml of 0.75% ropivacaine and 0.5 ml normal saline each for SSNB and ANB.

干预措施: Saline injection (Drug)

结局指标

主要结局

visual analog scale of pain

时间窗: change from baseline VAS pain score at hour 48

The VAS pain score was based on a scale from 0 to 10, where 0 indicated no pain and 10 indicated severe pain.

次要结局

  • Plasma cortisol level(change from baseline plasma cortisol level at hour 48)
  • patient's satisfaction(change from baseline patient's satisfaction score at hour 48)
  • Plasma IL-6 level(change from baseline plasma IL-6 level at hour 48)
  • Plasma serotonin level(change from baseline plasma serotonin level at hour 48)
  • Plasma IL-8 level(change from baseline plasma IL-8 level at hour 48)
  • Plasma IL-1β level(change from baseline plasma IL-1β level at hour 48)

研究者

发起方
Chuncheon Sacred Heart Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Jung-Taek Hwang

Associate Professor

Chuncheon Sacred Heart Hospital

研究点 (1)

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