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Ultrasound Guided QLB III Versus Intrathecal Morphine for Analgesia After Cesarean Section

Ultrasound Guided Quadratus Lumborum Type III Block Versus Intrathecal Morphine for Analgesia After Cesarean Delivery

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03428880
Acronym
QLB
Enrollment
120
Registered
2018-02-12
Start date
2017-02-15
Completion date
2017-10-20
Last updated
2018-02-14

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

Conditions

Block

Keywords

quadratus lumborum block, cesarean section, spinal morphine, ultrasound guidance

Brief summary

Subarachnoid morphine (SAM) is the gold standard for treating postoperative pain after cesarean delivery (CD) but it has undesirable side effects, that's why the aim of our study is to identify whether ultrasound-guided Quadratus lumborum block type 3, a new regional anesthetic technique that blocks the abdominal wall neural afferents, can provide at the same time better postoperative analgesia after CD with less side effects

Detailed description

In this prospective double blinded randomized study,120 parturients undergoing cesarian delivery via a Pfannenstiel incision and who agreed to spinal anesthesia were randomly scheduled to receive either a SAM (group SAM, n=60) or a Quadratus lumborum block type 3 (group QLB, n=60).Spinal anesthesia was initiated with hyperbaric Bupivacaïne 0.5% 10 mg, 0,005 mg SUFENTANIL MEDIS and 0.1 mg morphine in the SAM group and with Bupivacaïne 0.5% 10 mg, 0,005 mg SUFENTANIL MEDIS and 1 ml normal saline in group QLB. After surgery, bilateral QLB block type 3 was performed with the patient in lateral position using bupivacaine 0.25% , 20 mL on each side in group QLB and 20 ml normal saline in group SAM. Postoperative analgesia for the first 24 hours consisted of a patient controlled analgesia with IV morphine only. If necessary breakthrough pain was treated by 01 g paracetamol intravenously by the same doctor in charge of taking the values of the visual analogue scale. Patients were assessed postoperatively in the postanesthesia care unit (time 0 hours) and at 2, 4, 6, 12 and 24 hours. Visual analogue scale (VAS) for pain at rest and during the palpation of the uterine globe was noted. The primary outcome measure was the total dose of morphine over 24 hours delivered by a patient-controlled analgesia system at predetermined intervals. Secondary outcomes were visual analogue scale (VAS) for pain at rest and on the palpation of the uterine globe ,heart rate, blood pressure, itching, nausea, pruritus, vomiting and sedation.

Interventions

DRUGMorphine

spinal morphine is done before cesarean section

DRUGQuadratus lumborum block

a US Block QLB is done after surgery

Sponsors

University Tunis El Manar
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
FEMALE
Age
18 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* ASA I/II. * Normal singleton pregnancy with a gestation of at least 37 weeks.

Exclusion criteria

* Heart disease * Coagulopathy * pre-eclampsia * BMI\> 40 * Patient refusal to undergo the Quadratus lumborum block. * Allergy to local anesthetics

Design outcomes

Primary

MeasureTime frameDescription
Total morphine consumption over 24 hours postoperativelyArrival to post anesthesia care unit until 24 hours posterativelyTotal IV morphine used when started postoperatively using a PCA with morphine in the post anesthesia care unit until 2' hours posteratively.

Secondary

MeasureTime frameDescription
Time to first analgesic demand using PCA pump with morphineArrival to post anesthesia care unit until 24 hours posterativelyrecording the exact time to first analgesic demand by using the PCA with Morphine
Visual analog scale (VAS) pain scores at rest and during the palpation of the uterine globeArrival to post anesthesia care unit until 24 hours posterativelyAt predetermined intervalls, visual analog scale (VAS) pain scores at rest and at the palpation of the uterine globe were noted.
Time to first deambulaton after surgeryArrival to post anesthesia care unit until 24 hours posterativelyAfter surgery, time when the patient was able to move from bed was noted.

Countries

Tunisia

Outcome results

None listed

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