跳至主要内容
临床试验/CTRI/2024/08/073154
CTRI/2024/08/073154尚未招募不适用

Comparison of USG guided single injection Erector Spinae Plane Block versus Serratus Anterior Plane Block for postoperative analgesia in thoracic surgery A Randomised Control Trial

DR SN Medical College1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年9月4日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
The primary objective to compare SAPB or ESPB for postoperative analgesia following thoracic surgery, as determined by the time until the first analgesic requirement in the postoperative period

研究概览

简要总结

Comparison of  USG guided single injection erector spinae plane block versus serratus anterior plane block for postoperative analgesia in thoracic surgery.  Ultrasound-guided ESPB and SAPB are two most common analgesic methods that are simple, associated with high safety and good analgesic effect. The main objective of this study is to compare the efficiency of ultrasound-guided ESPB and SAPB for postoperative analgesia and inflammation control in patients.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
None

入排标准

年龄范围
18.00 Year(s) 至 45.00 Year(s)(—)
性别
All

入选标准

  • Â Adult patients, aged between 18 to 45 years and undergoing elective Thoracic surgeries under general anesthesia who belongs to ASA PSI, II.

排除标准

  • 1.Patients with BMI more than 30 kg/m2 or BMI less than 18 kg/m2 2.Patient refusal 3.Age less than 18 years old 4.Pregnant woman 5.History of any allergy to related perioperative medications 6.Previous lumbar spine surgery 7.Existing contraindications to nerve block such as coagulopathy, local and systemic infections 8.Those patients who are intubated for more than 4 hours postoperatively and shifted to postoperative ward will be excluded from the study 9. Patients who experience block failure 10.Those patients complaining of pain within 2 hours of postoperative period will be considered as block failure and are excluded from the study.

结局指标

主要结局

The primary objective to compare SAPB or ESPB for postoperative analgesia following thoracic surgery, as determined by the time until the first analgesic requirement in the postoperative period

时间窗: The primary objective to compare SAPB or ESPB for postoperative analgesia following thoracic surgery, as determined by the time until the first analgesic requirement in the first 24 hours postoperative period

次要结局

  • 1.VAS score at rest and while coughing at 2, 4, 8, 24, 48 hours postoperatively(2.Consumption of injection tramadol in first 24 hours of postoperative period)

研究者

发起方
DR SN Medical College
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Preetha V R

DR SN Medical College

研究点 (1)

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