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Transversus Abdominis Plane Block Plus Quadratus Lumborum Block or Retrolaminar Block of Multiple Injections for Postoperative Analgesia Following Laparoscopic Colorectal Surgery

Transversus Abdominis Plane Block Plus Quadratus Lumborum Block or Retrolaminar Block of Multiple Injections for Postoperative Analgesia Following Laparoscopic Colorectal Surgery: A Randomized, Double-blind, Controlled Trial

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05416866
Enrollment
100
Registered
2022-06-14
Start date
2022-06-20
Completion date
2022-12-30
Last updated
2022-06-14

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

Conditions

Analgesia, Colorectal, Laparoscopic, Quadratus Lumborum Block

Brief summary

Our hypothesis was that transversus abdominis plane block plus retrolaminar block would reduce postoperative sufentanil consumption and provide superior analgesia compared with transversus abdominis plane block plus quadratus lumborum block for laparoscopic colorectal surgery.

Interventions

PROCEDURERetrolaminar block on the operative side

After the skin near the puncture site was disinfected, 2ml of 1% lidocaine was injected into the puncture site for local infiltration. The needle was inserted beneath the ultrasound probe using an in-plane orientation to contact the lamina of the T8-T11 vertebra. Then we retracted the tip of needle to the lamina about 1 mm and withdrew to make sure that there was no blood or cerebrospinal fluid. Then, 30-40 mL mixture was injected posterior to the lamina of T8-T11.

PROCEDUREQuadratus lumborum block on the operative side

In our study, we applied a transmuscular approach to the QLB. After the patients were placed in the lateral position, the skin near the puncture site was disinfected, a low-frequency (3-5 MHz), curvilinear probe is used and is located vertical to the iliac crest at the posterior axillary line to find the Shamrock sign. After the local infiltration for puncture site, the 22-G needle is then inserted in plane and directed to the QL muscle. After the proper position of the needle tip between the psoas major muscle and the QL muscle is confirmed, 30 ml mixture is injected into the interfascial plane.

PROCEDURETransversus abdominis plane block on the nonoperative side

After placing the patients in the supine position, the skin was disinfected. A linear probe was placed in the transverse plane at the midaxillary line between the lower costal margin and iliac crest. When the external oblique, internal oblique, and transversus abdominis muscles were observed, 2ml of 1% lidocaine was injected into the puncture site for local infiltration.Then, a 22-gauge, 80-mm needle was advanced using an in-plane technique in an anteromedial to posterolateral direction toward the TAP (the fascial plane between the internal oblique and transversus abdominis muscles). After the correct position of the needle tip was verified, 20 ml mixture was injected into the TAP. The ultrasound showed that the local anesthetic separated the internal oblique and transversus abdominis muscles, confirming the success of the block.

Sponsors

dong zhang
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Except the regional anesthesiologist who performed the blocks, patients, surgeons, theatre anesthesiologists, ward staff, caregivers, and the outcome assessor were unaware of group allocation. The regional anesthesiologist was not involved in the other parts of the study. All data was collected by personnel blinded to the patient group allocation.

Intervention model description

A randomized, double-blind, controlled trial

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* American Society of Anesthesiologists (ASA) physical status I-II class * Colorectal cancer patients * 18 and 80 years old * Elective laparoscopic colorectal surgery

Exclusion criteria

* serious complications associated with other systems: * severe cardiac insufficiency * renal failure * hepatic encephalopathy * infection in the block injection area * coagulopathy * a known allergy to local anesthetics * a previous history of tranquilizer or opioid abuse, * body mass index (BMI) greater than 30 kg/m2 or less than 18 kg/m2, * inability to cooperate with the assessment of visual analogue scale (VAS) pain scores * refusal to participate in the study

Design outcomes

Primary

MeasureTime frameDescription
the cumulative consumption of sufentanil24 hours after nerves blockthe outcome in micrograms

Secondary

MeasureTime frameDescription
cumulative sufentanil consumption at predetermined time intervalswithin 24 hour after nerves blockthe outcome in minutes
time until the earliest single patient-controlled analgesia (PCA) dose of sufentanilwithin 24 hour after nerves blockthe outcome in minutes
the number of PCA presswithin 24 hour after nerves blockthe outcome in frequency
time until the earliest rescue analgesia and antiemeticwithin 24 hour after nerves blockthe outcome in minutes
the total dose of rescue analgesia and antiemeticwithin 24 hour after nerves blockthe outcome in milligrams
the patient's mean arterial pressure (MAP), HR at rest and during movement at 1, 2, 4, 6, 8, 12, 18, 24 after nerves blockthe time for completion of nerves block was time 0MAP in mmHg, HR in rate/one minute.
other side eventswithin 24 hour after nerves blocksuch as bradycardia (HR less than 60 beats per min), hypotension (systolic blood pressure less than 90 mmHg or more than 20% lower than baseline), hypoxemia (SpO2 less than 90%), respiratory depression (RR less than 10 breaths per min lasting for more than 10 min), pruritus, backache, nausea and vomiting
patient satisfaction with pain managementat 24th hour after nerves blockPatient satisfaction on postoperative analgesia using a 5-point scale (1 = very unsatisfied, 2 = unsatisfied, 3 = fair, 4 = satisfied, and 5 = very satisfied)
the length of hospital stayup to 2 weeksthe outcome in days
Visual Analog Score (VAS) for pain at rest and during movement at 1, 2, 4, 6, 8, 12, 18, 24 after nerves blockthe time for completion of nerves block was time 0The VAS is an internationally recognized scale for assessment of pain on an 11-point scale ranging from 0 to 10 points, with 0 defined as no pain and 10 defined as the worst pain imaginable (units on a scale)
block-related complicationswithin 24 hour after nerves blocksuch as hematoma, infection, quadriceps weakness, pneumothorax, deep visceral injury, and evidence of systemic toxicity to the local anesthetic

Outcome results

None listed

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