Study of effectiveness of Pre induction USG guided pericapsular nerve group(PENG) block in minimizing pain associated with positioning for neuraxial anesthesia in patients with hip fractures: A prospective randomized control study
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 32
- 试验地点
- 1
- 主要终点
- •To measure and compare the total duration taken for positioning till completion of neuraxial block to evaluate ease of execution and NPRS scoring
研究概览
简要总结
This study is a prospective randomized controlled study, double blind, trial comparing ultrasound guided pericapsular nerve group block with 0.25% ropivacaine and intravenous fentanyl for ease of positioning to administering neuraxial block and pain relief with patients undergoing hip fracture surgeries which will be conducted in Jaipur Golden Hospital in India.
The primary outcome is to measure and compare the total duration taken for positioning till completion of neuraxial block to evaluate ease of execution and NPRS scores. The secondary outcome Duration of postoperative analgesia by noting the time for first demand of analgesia after completion of 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
- 20.00 Year(s) 至 90.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients consenting for the intervention (PENG block) and regional anesthesia
- •Age 20 years to 90 years of either gender
- •ASA grade1,2 or 3.
排除标准
- •Patients’ refusal for regional anesthesia and if any contraindication is present.
- •Any strong contraindication for opioid analgesics like advanced chronic lung disease with respiratory failure, severe OSA etc
- •Allergy to any drug under study.
- •Patients with coagulopathy or on anticoagulants.
- •Patients with evidence of Cardiac failure.
- •Any infection at the site of block
- •Patient unable to communicate.
结局指标
主要结局
•To measure and compare the total duration taken for positioning till completion of neuraxial block to evaluate ease of execution and NPRS scoring
时间窗: Baseline, 30mins
次要结局
- To observe numerical pain rating scale (NPRS) score, before and after intervention (PENG block/IV opioid) and during positioning for spinal anaesthesia and compare the outcome of the cases with that of control group(Perioperative)
- To measure and compare the total duration taken for positioning till completion of neuraxial block to evaluate ease of execution.(Perioperative)
- To study whether preoperative PENG block has any influence on post operative analgesia by noting time for first demand of analgesia after completion of surgery(24-48 hours)
- To observe the hemodynamic changes from baseline till execution of neuraxial block in both the study and the control group and compare(Perioperative)
研究者
DR BEJOY S GEORGE
Jaipur Golden Hospital