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Quadratus Lumborum Block for Postoperative Analgesia After Colostomy Closure

Ultrasound-guided Quadratus Lumborum Block for Postoperative Analgesia After Colostomy: A Randomized Controlled Trial

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02691403
Enrollment
50
Registered
2016-02-25
Start date
2016-03-31
Completion date
Unknown
Last updated
2016-02-25

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

Conditions

Postoperative Pain

Brief summary

Patients undergoing abdominal procedures often require multimodal postoperative pain controls. Truncal blocks such as quadratus lumborum (QL) block may be used adjunctively as a part of it. The investigators hypothesized that the ultrasound-guided QL block with transmuscular approach can provide adequate pain relief for colostomy closure as part of a multimodal pain control.

Interventions

DRUGlevo-bupivacaine
DRUGnormal saline

Sponsors

Sun Yat-sen University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
20 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* A physical status between ASA I and III * 20 - 75 years of age * Patient has signed an informed consent * Without contraindication of QL block

Exclusion criteria

* American Society of Anesthesiologists (ASA) Physical Status ≥ 4 * Any contraindication to nerve blocks (including coagulopathy, abnormal anatomy, infection at the planned QL injection site, and amide-type local anesthetic allergy) pregnancy or breast-feeding * Severe obesity (body mass index≥ 35 kg/m2) * Patients with a history of significant neurological, psychiatric, neuromuscular, cardiovascular, pulmonary, renal or hepatic disease * Allergy to NSAIDs * Infection at the QL injection site * Patients with major psychosis or drug and alcohol abuse * Patient unable to comprehend or use the verbal rating pain scoring system or patient-controlled analgesia pump

Design outcomes

Primary

MeasureTime frame
cumulative morphine consumption1 hour

Outcome results

None listed

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