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