QL vs LAI for Palatoplasty

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age6-18
SponsorMedical University of South Carolina

About this trial

This study will consist of patients ages 6-18 who are undergoing a surgery on the hard or soft palate of the mouth (palatoplasty), with removal of bone from the front of the hip (anterior iliac bone graft harvesting). The patients will be randomized to receive either a unilateral QL block by an anesthesiologist, or local anesthetic infiltration at the surgical incision by the surgeon. The primary aim will be assessing post-operative pain in the first 48 hours after surgery. Secondary outcomes will include pain medication use in the first 48 hours after surgery, block resolution time, and evaluating any complications associated with the QL block or local anesthetic infiltration.

Eligibility criteria

Qualifiers

Patients undergoing palatoplasty with autologous bone graft from the anterior iliac crest.

Ages 6-18 years of age

Planned admission post-op

ASA Status Range: 1-3

Disqualifiers

overlying infection skin at the block needle insertion site

coagulopathies

known bleeding disorders

Allergy to local anesthetic

Trial design

Treatments tested in this trial

  • Quadratus lumborum block
  • Local anesthetic infiltration

Treatment groups

46 Participants
are divided into 2 treatment groups