46 Participants Needed

Nerve Block vs Local Anesthesia for Cleft Palate Surgery

HN
Overseen ByHaley Nitchie, MHA
Age: < 65
Sex: Any
Trial Phase: Academic
Sponsor: Medical University of South Carolina
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

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.12345

Why 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?

NM

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

I am having surgery to repair my palate using bone from my hip.
ASA Status Range: 1-3
I will be staying in the hospital after my surgery.

Exclusion Criteria

Non-English Speaking/Writing
Subjects or their parent/guardian unable or choose to not give informed consent/assent
I have difficulty reporting pain due to cognitive or developmental issues.
See 1 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

1-2 weeks

Treatment

Participants undergo palatoplasty surgery with either a QL block or local anesthetic infiltration for pain management

Immediate post-operative period
1 visit (in-person)

Post-operative Monitoring

Participants' pain scores and opioid consumption are monitored for 48 hours post-surgery

48 hours

Follow-up

Participants are monitored for block resolution and any complications up to 7 days post-surgery

7 days

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?
2Treatment groups
Active Control
Group I: Local anesthetic infiltrationActive Control1 Intervention
Group II: Quadratus lumborum blockActive Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Medical University of South Carolina

Lead Sponsor

Trials
994
Recruited
7,408,000+

Published Research Related to This Trial

In a study involving 60 children undergoing cleft palate repair, both levobupivacaine and bupivacaine were found to be equally effective for pain management, with no significant differences in pain scores or serious complications.
Bilateral maxillary nerve block (MNB) using either anesthetic provided effective pain relief, highlighting it as a safe and straightforward method for managing postoperative pain in children after cleft palate surgery.
Comparative study of levobupivacaine and bupivacaine for bilateral maxillary nerve block during pediatric primary cleft palate surgery: a randomized double-blind controlled study.Mostafa, MF., Herdan, R., Elshazly, M.[2019]
The study identified the average location of the infraorbital foramen in pediatric populations, finding it within 2 mm of a midpoint between the nasospinale and jugale across different age groups, which can help improve the accuracy of infraorbital nerve blocks for pain management after cleft lip surgery.
This information is particularly valuable in settings with limited access to ultrasound technology, ensuring that healthcare providers can perform effective nerve blocks even in developing countries.
Infraorbital foramen location in the pediatric population: A guide for infraorbital nerve block.Zdilla, MJ., Russell, ML., Koons, AW.[2019]
The quadratus lumborum block (QLB) is a safe and effective method for providing long-lasting pain relief, as demonstrated in a case involving a 3-year-old patient who underwent inguinal hernia repair.
The use of ultrasound guidance in administering the QLB allows for precise delivery of local anesthetic, resulting in successful postoperative analgesia and high family satisfaction with the patient's pain management.
Ultrasound-guided quadratus lumborum block for postoperative analgesia in a pediatric patient.Öksüz, G., Gürkan, Y., Urfalıoglu, A., et al.[2020]

Citations

1.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/34019509/
A Nationwide Analysis of Cleft Palate RepairBackground: This study investigates the associations between local anesthesia practice and perioperative complication, length of stay, ...
Perioperative pain management for cleft palate surgeryThe 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 ...
Adult Cleft Lip Repair Under Local AnesthesiaAdult 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 - PMCThis 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 surgeryThe aim of this review was to evaluate the available evidence and to develop recommendations for optimal pain management after cleft palate surgery.
Unbiased ResultsWe believe in providing patients with all the options.
Your Data Stays Your DataWe only share your information with the clinical trials you're trying to access.
Verified Trials OnlyAll of our trials are run by licensed doctors, researchers, and healthcare companies.
Terms of Service·Privacy Policy·Cookies·Security