跳至主要内容
临床试验/CTRI/2024/10/075118
CTRI/2024/10/075118尚未招募3 期

Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery

NAVYA KS1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2024年10月30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
40
试验地点
1
主要终点
Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery by administration of Bupivacaine comparison between the two groups Post operative pain scores (VAS)and Time to first rescue analgesia will be assesssed.

研究概览

简要总结

Purpose of study is to compare duration of analgesic efficacy of Superficial cervical plexus block versus Clavipectoral fascia block for perioperative pain management in clavicular surgery .

Hypothesis Clavipectoral fascia block have a equal analgesic efficacy as of Superficial cervical plexus block for clavicular surgery.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

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

入选标准

  • 1.ASA grade I or II fit patients.
  • Ages between 18 and 65 years
  • Patients undergoing clavicle surgeries.
  • Haemodynamically stable patients with all routine investigations within normal limits without any other co morbidities.
  • Patients who are not on any cardiac related drugs.
  • Availability of written informed consent from concerned patient.

排除标准

  • Patients not willing to participate in this study.
  • Patients with ASA physical status III and above physical status.
  • Patients less than 18 years and above 65 years of age.
  • Patients with uncontrolled systemic disorders like neurological, cardiac, metabolic, renal, pulmonary disorders, hepatic disease with coagulation abnormalities etc.
  • 5.Patients having local infection at the site where needle for block was to be inserted 6.Patients with bleeding or coagulation disorders.

结局指标

主要结局

Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery by administration of Bupivacaine comparison between the two groups Post operative pain scores (VAS)and Time to first rescue analgesia will be assesssed.

时间窗: After administration of the block ,comparison between the two groups of duration of analgesia, Post operative pain scores (VAS) at 8,12,16,20,24 hrs,Time to first rescue analgesia will be assesssed.

次要结局

  • Comparison of analgesic efficacy of superficial cervical plexus block versus clavipectoral fascia block for perioperative pain management in clavicular surgery by perineural administration of Bupivacaine.(After primary outcome comparison between the two groups of duration of analgesia & time to first rescue analgesia within 24 hr will also be assesssed.)

研究者

发起方
NAVYA KS
申办方类型
Other [(self)]
责任方
Principal Investigator
主要研究者

Dr. Navya KS

DR.D.Y.Patil Medical College,Hospital and Research Centre ,Pune

研究点 (1)

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