Pectoral Block for Pain Control in Breast Reduction
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores a new method for managing pain after breast reduction surgery. It tests whether the PEC II block, a type of nerve block, can match the effectiveness of the usual narcotic-based method while causing fewer side effects. This approach could reduce issues such as nausea and dependency associated with narcotics. Women experiencing symptoms from large breasts, like neck or shoulder pain, and considering breast reduction surgery might be suitable for this trial. Participants should have experienced these symptoms affecting daily life for at least a year. As a Phase 4 trial, the research aims to understand how an already FDA-approved and effective treatment can benefit more patients.
Do I need to stop my current medications for the trial?
The trial information does not specify if you need to stop taking your current medications. However, it mentions that participants should have tried other pain management methods like NSAIDs or muscle relaxants for at least 3 months before surgery.
What is the safety track record for the Pectoral II Nerve Block treatment?
Studies have shown that the Pectoral II nerve block offers promising results for controlling pain after breast surgery. Research indicates it can significantly reduce pain following breast reduction surgery and decrease the need for opioid painkillers. This is important because opioids often cause side effects like nausea and carry a risk of addiction.
The Pectoral II block involves injecting a numbing medicine into a specific area of the chest. Multiple studies have found this method to be generally safe and effective, with no serious side effects reported. Patients who received the Pectoral II block experienced less pain and used fewer opioids compared to those who did not receive the block.
Overall, the Pectoral II nerve block appears well-tolerated, making it a good option for managing pain after breast reduction surgery.12345Why are researchers enthusiastic about this study treatment?
Researchers are excited about the Pectoral II nerve block for pain control in breast reduction surgeries because it offers a new approach to managing postoperative pain. Unlike the traditional method where a wetting solution with lidocaine and epinephrine is used, the Pectoral II block utilizes a combination of 0.25% bupivacaine with epinephrine, dexmedetomidine, and dexamethasone. This combination aims to provide targeted pain relief directly to the nerves, potentially reducing the need for narcotics and enhancing recovery. By focusing on nerve blocks, this method could offer more effective pain control with fewer side effects compared to standard options.
What evidence suggests that the Pectoral II Nerve Block is effective for pain control in breast reduction?
This trial will compare the effectiveness of the PECS II block with a control group for pain management in breast reduction surgery. Research has shown that the PECS II block can significantly reduce pain after breast surgery. Studies have found that patients receiving this block report less pain and require fewer pain medications post-surgery. For instance, one study found that the PECS II block provided much better pain relief compared to not using it. Another study highlighted that it reduces the need for opioids, which are strong painkillers often associated with side effects. Overall, the PECS II block appears to offer effective pain control for breast surgeries.16789
Who Is on the Research Team?
Anthony Capito, MD
Principal Investigator
Carilion Clinic
Are You a Good Fit for This Trial?
This trial is for women aged 18–75 with very large breasts causing symptoms like back, neck, or shoulder pain who are scheduled for breast reduction surgery. Participants must have stable breast size for at least a year and meet certain health requirements, including recent mammograms if over age 50.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants undergo breast reduction surgery with either PECs II block or standard multimodal pain control
Postoperative Monitoring
Participants are monitored for pain control and narcotic usage through surveys on days 1, 3, and 7 post-surgery
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Pectoral II Nerve Block
Trial Overview
The study compares two ways to manage pain after breast reduction: one group gets a nerve block (Pectoral II Block) alone, while the other receives standard pain control that includes narcotic medications. The goal is to see if the nerve block works as well as traditional methods.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Patients receive wetting solution with only epinephrine in both breasts at the beginning of the case for hemostasis. The patient will be administered 20 cc's of local anesthetic (0.25% bupivacaine with epinephrine), with 20 mcg dexmedetomidine and 4 mg dexamethasone added per breast. A total of 40 cc's of 0.25% bupivacaine will be used. This will be performed as a Pectoral II block. As needed narcotic paper prescription is provided, same as in the control group.
Patients receive wetting solution with lidocaine and epinephrine in both breasts at the beginning of the case for analgesia and hemostasis. No nerve block is administered intraoperatively. As needed narcotic paper prescription is provided, same as in the experimental group.
Find a Clinic Near You
Who Is Running the Clinical Trial?
Carilion Clinic
Lead Sponsor
Citations
Comparison of the Effects of Pectoral Nerve Block and Local ...
... Pecs II block significantly reduced postoperative pain after breast reduction surgery. It was also observed that intraoperative and postoperative analgesic ...
Efficacy of PECS block in addition to multimodal analgesia for ...
Pectoralis nerve blocks (PECS) have been shown in numerous studies to be a safe and effective method to treat postoperative pain and reduce postoperative opioid ...
3.
journals.lww.com
journals.lww.com/md-journal/fulltext/2023/02220/the_efficacy_of_pectoral_nerve_block_for_pain.54.aspxThe efficacy of pectoral nerve block for pain control after .. ...
Compared with control group after breast augmentation, pectoral nerve block was associated with substantially reduced pain scores at 1 hour ( ...
Efficacy of pectoralis nerve blocks I & II with liposomal ...
The purpose of this study was to evaluate the effect of performing PECs blocks with LB for patients undergoing breast reduction procedures. The primary outcome ...
PECS II block is associated with lower incidence of chronic ...
This block can provide good anesthesia for the breast and axilla region; however, it is usually unable to cover the parasternal branches of the ...
Evaluation of the Efficacy of Pectoral Nerve-2 Block (PECS ...
This study aimed to evaluate the efficacy of the pectoral nerves interfacial plane block (PECS II) in breast cancer surgery focusing on postoperative pain ...
Pectoral Block in Breast Reduction for Pain Control
The Pectoral II block is a modified Pectoral I block and can be achieved using a single needle stick. Local anesthetic placement is between the pectoralis major ...
PECS II block is associated with lower incidence of chronic ...
In conclusion, our study suggests that the PECS II block could be able to prevent chronic pain after breast surgery at 3 months after surgery.
Efficacy of PECS block in addition to multimodal analgesia ...
Pectoralis nerve blocks (PECS) have been shown in numerous studies to be a safe and effective method to treat postoperative pain and reduce postoperative opioid ...
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