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
Trial Overview
The study compares two types of pain relief methods after palatoplasty: a 'QL block' given by an anesthesiologist versus a local anesthetic directly at the surgical site by the surgeon. It will measure how well each method controls pain in the first two days post-surgery and monitor any complications.
How Is the Trial Designed?
2
Treatment groups
Active Control
Patient will undergo induction of anesthesia as deemed appropriate by the attending pediatric anesthesiologist assigned to the case. After induction of anesthesia and securement of appropriate airway device the patient will be turned over to the surgical team to proceed with the operation. The surgeon will proceed with usual injection of local anesthetic as their standard of care; this medication will be charted by the circulating nurse in the Medication Administration Record with local anesthetic type and amount. At the conclusion of the procedure, to maintain the blind, the patient will have a bandage placed where the QL block would have been performed.
After induction of anesthesia and securement of appropriate airway device, the patient will be placed in position for the QL block. Using ultrasound guidance, the pediatric anesthesiology attending will perform unilateral QL block on the side of the anterior iliac bone graft harvest. The dose will be 0.2% ropivacaine, 1 mL per kilogram to a max of 20 mL with an additive of dexamethasone 4 mg. Ultrasonography will be used to identify external oblique, internal oblique, transverse abdominus and quadratus lumborum muscles. A 50 mm-150 mm block needle will be advanced under ultrasound guidance. Ropivacaine will be injected slowly with frequent aspiration to rule out incorrect needle placement. The anesthetic is deposited at the lateral edge of the QL after penetrating the transversus abdominus aponeurosis. Injection will continue to be observed with real time US guidance.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Medical University of South Carolina
Lead Sponsor
Published Research Related to This Trial
Citations
A Nationwide Analysis of Cleft Palate Repair
Background: This study investigates the associations between local anesthesia practice and perioperative complication, length of stay, ...
Perioperative pain management for cleft palate surgery
The aim of this review was to evaluate the available evidence and to develop recommendations for optimal pain management after cleft palate surgery.
Comparison of postoperative analgesia in children ...
Local infiltration with ropivacaine effectively provided postoperative analgesia for children undergoing cleft palate repair without major side effects.
Use of Local Anesthesia in Adolescent and Adults ...
Most patients reported minimal to no pain and required no general anesthesia during the procedures. Conclusions. The current literature supports ...
5.
gsmile.org
gsmile.org/wp-content/uploads/2020/08/2013-Adult-Cleft-Lip-Repair-Under-Local-Anesthesia-CPCJ.pdfAdult Cleft Lip Repair Under Local Anesthesia
Adult cleft lip surgery is safe and effective with the use of local anesthesia alone, and improvements in technique and efficiency have made this valuable for ...
Anaesthesia for cleft lip and palate surgery - PMC
This review aims to provide an overview of cleft lip and palate, and considerations for anaesthesia and perioperative management of these patients.
Anesthetic Approach and Perioperative Complications in ...
Results: The number of anesthesia complications was higher in patients with difficult mask ventilation. Surgical complica- tions were more ...
Perioperative pain management for cleft palate surgery
The aim of this review was to evaluate the available evidence and to develop recommendations for optimal pain management after cleft palate surgery.
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