Post-operative Analgesia Efficacy Using Ultrasound-guided Transmuscular Quadratus Lumborum Block Versus Ultrasound-guided Quadratus Lumborum Type II Block.
- Registration Number
- NCT03100994
- Lead Sponsor
- Tri-Service General Hospital
- Brief Summary
Post-operative analgesia efficacy using ultrasound-guided transmuscular quadratus lumborum block versus ultrasound-guided quadratus lumborum type II block
- Detailed Description
The Quadratus Lumborum (QL) Block is an ultrasound-guided technique described by Rafael Blanco in 2007. The nerves to the lower abdominal wall can be anesthetized by injecting local anesthetics between the quadratus lumborum muscle and latissimus dorsi muscle, which is called quadratus lumborum type II block. 〝 Transmuscular quadratus lumborum block demonstrates that injectate spreads over the posterior abdominal wall to the psoas major muscle and includes the upper branches of the lumbar plexus.〞described by Adhikary in 2016. However there are no published reports comparing the 2 techniques. In our study, compared of ultrasound-guided QL2-blocks with transmuscular quadratus lumborum block to investigate analgesic consumption, pain level, opioid related side effects and mobilization.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 180
- American Society of Anesthesiologists classification (ASA) 1~3
- adequate communication skills
- Body mass index < 32
chronic pain neurological illness/ neuropathy contraindication against local anesthetics
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Group B Bupivacaine Ultrasound guided transmuscular quadratus lumborum block with 0.125% bupivacaine 30ml Group C Ultrasound Ultrasound guided quadratus lumborum type 2 block with 0.125% bupivacaine 30ml Group B Ultrasound Ultrasound guided transmuscular quadratus lumborum block with 0.125% bupivacaine 30ml Group C Bupivacaine Ultrasound guided quadratus lumborum type 2 block with 0.125% bupivacaine 30ml
- Primary Outcome Measures
Name Time Method morphine consumption 48 hours morphine consumption
- Secondary Outcome Measures
Name Time Method Nausea or vomiting 48 hours Severity of nausea or vomiting in the first 48 hours after surgery. Severe :3 Moderate:2 Mild:1 None: 0
Skin itch 48 hours Severity of skin itch in the first 48 hours after surgery. Severe :3 Moderate:2 Mild:1 None: 0
Severity of postoperative pain via visual analogue pain scale (VAS) 48 hours Total cumulative morphine dose in mg used in the first 48 hours after surgery
time to mobilization 48 hours Time to mobile in the first 48 hours after surgery
Trial Locations
- Locations (1)
Tri-Service General Hospital
🇨🇳Taipei, Taiwan