CTRI/2021/10/037221尚未招募不适用
A comparative evaluation of analgesic efficacy of Serratus anterior with Erector spinae fascial plane block along with General Anaesthesia for Breast cancer surgery
未提供1 个研究点 分布在 1 个国家目标入组 100 人开始时间: 2021年12月10日最近更新:
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 100
- 试验地点
- 1
- 主要终点
- Post op pain scores [Time frame: 24 hours post op] Patients level of post op pain will be evaluated using visual analogue scale (VAS). Range between 0- 10.
研究概览
简要总结
This is a prospective randomised interventional parallel group trail where patients will be divided in two groups. We will compare the efficacy of Serratus anterior vs Erector spinae fascial plane block along with General anaesthesia for breast cancer surgery. Also we will assess the decrease in the use of intra operative and post operative analgesics.
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Open Label
入排标准
- 年龄范围
- 18.00 Year(s) 至 65.00 Year(s)（—）
- 性别
- Female
入选标准
- •1 All female non pregnant patients 18-65 years of age with no comorbidities 2 ASA class I-II 3 BMI < 35kg/m2 4 Having unilateral breast cancer that may or may not involve the axilla.
排除标准
- •1 ASA class lll-Vl 2 BMI>35kg/m2 3 Patient refusal 4 Allergy to ropivacaine or fentanyl 5 Patients undergoing breast reconstruction surgery 6 Prior ipsilateral breast surgery, excluding lumpectomy 7 Pre-existing neurological deficit or peripheral neuropathy involving the ipsilateral chest 8 Severe, poorly controlled cardiac and respiratory conditions like arrhythmias, valvular heart diseases, COPD, Interstitial lung disease, poorly controlled asthma 9 Contraindication to regional or general anaesthesia (e.g. bleeding diathesis, coagulopathy, sepsis, infection at the site of potential needle puncture) 10 Pre-existing chronic pain disorder 11 Significant psychiatric disorder that would preclude objective study assessment 11 Pregnancy 12 Unable to provide informed consent.
结局指标
主要结局
Post op pain scores [Time frame: 24 hours post op] Patients level of post op pain will be evaluated using visual analogue scale (VAS). Range between 0- 10.
时间窗: Post op pain scores [Time frame: 24 hours post op] Patients level of post op pain will be evaluated using visual analogue scale (VAS). Range between 0- 10.
次要结局
- 1Sensory block onset assessment- pinprick sensation test [Time frame- End of surgical procedure until 24 hours post op](2 Mean analgesic consumption [Time frame- 24 hours post op] Cumulative I/V Tramadol or PCM 1gm equivalent after surgery)
研究者
研究点 (1)
Loading locations...
相似试验
已完成
4 期
Efficacy on Pain Following a Procedure for Injecting Sclerotherapeutic Foam Into the Great Saphenous VeinVenous DiseaseNCT01368159Le Club Mousse120
尚未招募
不适用
comparing two different postoperative analgesic methods-epidural technique versus a combination of analgesic methodsCTRI/2021/12/039016Sri Lakshmi Narayana Institute of Medical Sciences100
尚未招募
不适用
Comparison of Ropivacaine with Dexmedetomidine versus Ropivacaine with Magnesium Sulfate for Pain Relief After Lumbar Spine SurgeryCTRI/2025/04/084862SMS Medical College And Hospital120
已完成
3 期
A Comparison of the Analgesic Efficacy and Safety of Once Daily Tramadol HCl / Contramid® Tablets to Twice Daily Tramadol HCl (SR) for the Treatment of Osteoarthritis of the KneePainOsteoarthritis, KneeNCT00950651Labopharm Inc.431
终止
4 期
A Study Comparing Two Analgesia/Sedation Regimens, Remifentanil/Propofol Versus Sufentanil/Propofol In Mechanically Ventilated Intensive Care Patients Requiring Analgesia And Sedation.AnalgesiaSedationNCT00421720GlaxoSmithKline164