Trials / Completed
CompletedNCT04800302
U/S-guided Continuous Quadratus Lumborum Block III in Percutaneous Nephrolithotomy
Ultrasound-guided Continuous Quadratus Lumborum Block III for Postoperative Analgesia in Percutaneous Nephrolithotomy
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 45 (actual)
- Sponsor
- Nazmy Edward Seif · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
Percutaneous nephrolithotomy (PCNL) is considered to be the first choice and a more conservative procedure than open stone surgery. Not only postoperative pain related to dilatation of the renal capsule and parenchymal tract, but also patient's discomfort \& nephrostomy tube-related stress are reported to delay recovery time and increase the complication rates. This study is designed to provide postoperative analgesia by using ultrasound-guided continuous Quadratus Lumborum Block (QLB) III in patients undergoing PCNL and to assess pain scores \& side effects with less opioids consumption.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| PROCEDURE | Continous Quadratum Lumborum Block III | Continuous infusion of Bupivacaine 0.125 % at a rate of 0.1 ml/kg/hr (not exceeding 12 ml/hour), infused through a catheter inserted in the plane between quadratus lumborum \& psoas major muscles with ultrasound guidance. |
| PROCEDURE | Single dose Quadratum Lumborum Block III | Single injection of a mixture solution of 20 ml Bupivacaine 0.5% + 10 ml Lidocaine 2%, injected through a needle inserted at the posterior aspect of the quadratus lumborum muscle between it and erector spinae muscle with ultrasound guidance. |
| PROCEDURE | Intra-venous Morphine | Intra-venous Morphine \[0.1 mg/kg\] as rescue analgesic shots when the Visual Analogue Score (VAS) for pain exceeds 4. |
Timeline
- Start date
- 2021-06-10
- Primary completion
- 2022-06-28
- Completion
- 2022-06-28
- First posted
- 2021-03-16
- Last updated
- 2022-07-22
Locations
1 site across 1 country: Egypt
Source: ClinicalTrials.gov record NCT04800302. Inclusion in this directory is not an endorsement.