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Analgesia of Erector Spinae Plane Block Versus Quadratus Lumborum Block

A Comparative Study of Analgesic Effect of Ultrasound Guided Erector Spinae Plane Block Versus Quadratus Lumborum Block for Open Colorectal Cancer Surgeries

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03803267
Enrollment
68
Registered
2019-01-14
Start date
2019-05-01
Completion date
2020-04-01
Last updated
2020-04-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Cancer

Brief summary

Colorectal cancer is the third most common cancer worldwide. These patients usually undergo open surgical resection of cancer under general anaesthesia. The aim of this study is to detect whether the Erector spinae plan block or Quadratus lumborum block will provide the most ideal analgesia for these patients. Erector spinae plan block is a novel analgesic technique that provides both visceral and somatic analgesia due to its communication with the paravertebral space. Quadratus lumborum block is a truncal nerve block usually used for intra-abdominal surgeries. Ultrasound guidance increases the accuracy and safety of both techniques. A local anaesthetic mixture of Bupivacaine 0.25% and dexamethasone will be used for both techniques.

Detailed description

Erector spinae plane block and quadratus lumborum block are analgesic techniques suitable for open colorectal cancer surgeries. postoperative pain score, serum levels of biomarkers of stress (cortisol and CRP), primary hemodynamics, time to first rescue analgesic request, the total amount of rescue analgesic consumption and postoperative nausea and vomiting are the parameters of comparison between both techniques.

Interventions

OTHERErector spinae plane block

For each side, the eighth thoracic transverse process will be identified by a linear US transducer (HFL38\_10-5 MHz), puncture will be performed in the plane in the craniocaudal direction until the needle contacts the transverse process, and 20 ml of bupivacaine 0.25% and 4 mg dexamethasone will be injected visualizing the hydrodissection. After 30 minutes, the degree of sensory block in the trunk will be assessed by the pinprick test and any undesirable motor weakness will be recorded as a side effect.

OTHERQuadratus lumborum block

For each side, shamrock sign with three leaves (psoas major muscle anteriorly, the erector spinae muscle posteriorly and the quadratus lumborum muscle adherent to the apex of the transverse process of the L4 vertebral body) will be identified by a curved array US transducer (6-2MHz), puncture will be performed in-plane, the needle will be advanced through the quadratus lumborum muscle penetrating the ventral proper fascia of the quadratus lumborum muscle, and 20 mL of bupivacaine 0.25% and 4 mg dexamethasone will be injected in that space visualizing the hydrodissection. After 30 minutes, the degree of sensory block in the trunk will be assessed by the pinprick test and any undesired motor weakness will be recorded as a side effect

DRUGPropofol

Propofol (2 mg/kg)

DRUGFentanyl NCS

Fentanyl (1µg/Kg)

DRUGAtracurium Injectable Product

atracurium (0.5mg/kg)

OTHEREndotracheal intubation

endotracheal intubation

Inhalational isoflurane in oxygen/air mixture

DRUGMuscle Relaxation

atracurium boluses (0.2 mg/Kg/20 minutes) will be used for maintenance of general anesthesia

Sponsors

Mansoura University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
SINGLE (Subject)

Masking description

Single blind (participant) study

Eligibility

Sex/Gender
ALL
Age
40 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* American Society of Anesthesiologists physical status I or II * Body mass index from 18.5 to 35 Kg/m2

Exclusion criteria

* Body mass index more than 35 Kg/m2. * Severe or uncompensated cardiovascular disease. * Severe renal disease. * Severe hepatic disease. * Severe endocrinal disease. * Pregnancy. * Postpartum. * Lactating females * Allergy to one of the agents used. * Refusal to participate in the study.

Design outcomes

Primary

MeasureTime frameDescription
Postoperative pain scoreFrom 1 day before the surgery to the 2 days after surgeryThe intensity of pain indicated by a segmented numeric scale in which a respondent selects a whole number (0-100 integers) that best reflects his/her pain as 0-30 for mild pain, 30-60 for moderate pain and 60-100 for sever pain

Secondary

MeasureTime frameDescription
Mean Blood PressureOne hour before induction of general anesthesia, every 10 minutes till end of surgery, every 4 hours till end of the first 24 hours postoperatively, then every 8 hours till end of the next 24 hours: The average pressure in the arteries during one cardiac cycle. It is a better indicator for vital organs' perfusion than the systolic pressure
Heart rateOne hour before induction of general anesthesia, every 10 minutes till end of surgery, every 4 hours till end of the first 24 hours postoperatively, then every 8 hours till end of the next 24 hoursThe number of heart beats per minute. A lower heart rate at rest implies a more efficient heart function, better cardiovascular fitness and less stress
Time to first rescue analgesic requestUp to 48 postoperative hoursThe time elapsed from termination of performing each block till the patient's request for analgesia. It resembles the duration of analgesia
Peripheral oxygen saturationOne hour before induction of general anesthesia, every 10 minutes till end of surgery, every 4 hours till end of the first 24 hours postoperatively, then every 8 hours till end of the next 24 hoursAn estimate of oxygenated hemoglobin concentration in blood. It is measured by pulse oximeter device
Systolic Blood PressureOne hour before induction of general anesthesia, every 10 minutes till end of surgery, every 4 hours till end of the first 24 hours postoperatively, then every 8 hours till end of the next 24 hoursThe pressure in the arteries during contraction of the heart
Postoperative nausea and vomiting intensity scoreImmediately after recovery, every 4 hours till end of the first 24 hours postoperatively, then every 8 hours till end of the next 24 hoursPostoperative Nausea and Vomiting Intensity Scale: A scale that evaluates postoperative nausea and vomiting. It equals severity of nausea (1=mild, 2= moderate, 3= sever) x pattern of nausea (1=varying, 2= constant) x duration of nausea (in hours). At any time, if it is \< 50 or vomiting occurs once or twice, it is clinically unimportant (good outcome). If it is ≥50 or vomiting occurs 3 or more times, it is clinically important (bad outcome). The sum of all values will quantify the entire period of the study.
CortisolAt 9 Am, 1 hour after induction of general anesthesia, 1st, 24th and 48th hours postoperativelyA steroid hormone secreted by adrenal cortex in response to stress and hypoglycemia
Serum C-reactive protein (CRP)On hospital admission, 1 hour after induction of general anesthesia, 1st, 24th and 48th hours postoperativelyA protein synthetized by hepatocytes in response to systemic inflammation or tissue damage
Total amount of rescue analgesic consumptionFrom the time of first analgesic request till the end of the first 24 hours, then till the end of the next 24 hours postoperativelyThe total amount of morphine consumed by the patient for pain relief over the 48 hours postoperatively

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026