Nerve Block vs Local Anesthesia for Cleft Palate Surgery
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial aims to determine which pain control method is more effective for children and teens after cleft palate surgery. It compares two treatments: a nerve block (a type of pain relief given near the spine, specifically the quadratus lumborum block) and a local anesthetic (a numbing medicine applied directly to the surgical area, known as local anesthetic infiltration). The main focus is on the level of pain patients experience in the first two days after surgery. Eligible participants include children and teens aged 6-18 undergoing cleft palate surgery with bone taken from their hip. As an unphased trial, this study allows participants to contribute to valuable research that could enhance pain management for future patients.
Will I have to stop taking my current medications?
The trial information does not specify whether you need to stop taking your current medications. It's best to discuss this with the trial coordinators or your doctor.
Is there any evidence suggesting that this trial's treatments are likely to be safe?
Previous studies have shown that local anesthetic is well-tolerated during procedures. Most patients reported little to no pain and did not need extra anesthesia, indicating the treatment's safety and minimal complications.
Research shows the quadratus lumborum (QL) block is a safe and effective method for pain relief. It has been used successfully for long-lasting pain control in surgeries. Some studies indicate it reduces the need for opioids, which are strong painkillers, after surgery, highlighting its potential for managing pain with fewer side effects.
Overall, both treatments have been studied and found safe and effective for managing pain during surgery. They aim to minimize discomfort and reduce the need for additional medications.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it explores two different pain management techniques for cleft palate surgery: local anesthetic infiltration and the quadratus lumborum (QL) block. Unlike traditional methods that rely on direct injection of anesthetic into the surgical site, the QL block targets deeper nerves using ultrasound guidance, potentially offering more effective and longer-lasting pain relief. This method could reduce the need for additional pain medications and improve recovery times. By comparing these approaches, the trial aims to identify whether the QL block can enhance surgical outcomes and patient comfort compared to the standard local anesthetic infiltration.
What evidence suggests that this trial's treatments could be effective for post-operative pain in cleft palate surgery?
This trial will compare the effectiveness of local anesthetic infiltration with the quadratus lumborum (QL) block for managing pain after cleft palate surgery. Research has shown that local anesthetic can effectively manage pain after cleft palate surgery, providing good pain relief without major side effects. Most patients experience little to no pain and often don't need extra anesthesia. The QL block has also successfully reduced pain after various surgeries, decreasing the need for opioids and lowering pain levels, particularly in hip and abdominal surgeries. Both treatments in this trial have shown promising results in providing pain relief and are considered effective.35678
Who Is on the Research Team?
Nicole McCoy, M.D.
Principal Investigator
Medical University of South Carolina
Are You a Good Fit for This Trial?
This trial is for children and teenagers aged 6-18 who are having surgery on the roof of their mouth, which may also involve taking bone from the hip. Participants must be suitable for either a QL block or local anesthetic as part of their pain management after surgery.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo palatoplasty surgery with either a QL block or local anesthetic infiltration for pain management
Post-operative Monitoring
Participants' pain scores and opioid consumption are monitored for 48 hours post-surgery
Follow-up
Participants are monitored for block resolution and any complications up to 7 days post-surgery
What Are the Treatments Tested in This Trial?
Interventions
- Local anesthetic infiltration
- Quadratus lumborum block
Find a Clinic Near You
Who Is Running the Clinical Trial?
Medical University of South Carolina
Lead Sponsor