Nerve Block Techniques for Postoperative Pain from Knee Surgery
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial tests a new method for managing pain after knee replacement surgery. It examines whether adding an extra nerve block, which numbs specific nerves, can enhance pain relief and help patients move sooner post-surgery. The researchers compare the current standard nerve block with a combination approach that includes the new Femoral Triangle Block (FTB). Ideal participants are adults undergoing a first-time knee replacement and not on heavy daily pain medication. As an unphased trial, this study allows patients to contribute to innovative pain management strategies that could improve recovery experiences for future knee replacement patients.
Will I have to stop taking my current medications?
The trial protocol does not specify whether you need to stop taking your current medications. However, if you are taking more than 60 mg of morphine daily for chronic pain, you would not be eligible to participate.
What prior data suggests that these nerve block techniques are safe for postoperative pain management?
Research has shown that nerve blocks like the femoral triangle block (FTB) and the para-sartorial compartments block (PACS) are generally well-tolerated during knee surgery. These methods effectively manage pain without significantly affecting movement. The PACS block targets additional nerve areas not reached by the FTB alone, potentially improving pain relief.
When combined with the IPACK block, which focuses on the back of the knee, these techniques aim to provide comprehensive pain management. Previous studies reported few side effects. Medications used, such as ropivacaine, are usually safe, with only mild side effects like temporary numbness or soreness at the injection site. This combination of nerve blocks is considered safe based on current research and helps patients recover faster with better pain control.12345Why are researchers excited about this trial?
Researchers are excited about this trial because it explores innovative nerve block techniques for managing postoperative pain after knee surgery. Unlike the standard femoral triangle block (FTB) combined with IPACK, which is commonly used now, the experimental approach adds two additional ropivacaine injections in the subsartorial and suprasartorial compartments. This multi-site injection strategy aims to enhance pain relief by targeting more areas involved in knee sensation. By potentially offering more comprehensive pain management, these techniques could improve patient comfort and recovery time following knee surgery.
What evidence suggests that this trial's nerve block techniques could be effective for postoperative pain from knee surgery?
In this trial, one group of participants will receive a combination of the femoral triangle block (FTB) with the IPACK block. Previous studies have shown that this combination effectively relieves early pain after knee surgery and improves quadriceps muscle function. The IPACK block targets the sensory nerves behind the knee to ease pain in that area, while the FTB reduces pain without affecting leg movement. Another group will receive an additional para-sartorial compartments block, which research indicates can further improve pain relief by covering additional nerve areas not addressed by the FTB alone. Together, these blocks aim to offer better pain control, helping patients move more easily after surgery. This approach has been highlighted for its potential to enhance pain management while preserving leg strength.12367
Who Is on the Research Team?
Maxim Roy, MD, FRCPC
Principal Investigator
Centre hospitalier de l'Université de Montréal (CHUM)
Are You a Good Fit for This Trial?
This trial is for adults over 18 needing a primary total knee replacement, with an 'American Society of Anesthesiologists' classification of 1 to 3. It's not for those who can't consent or communicate with the team, don't understand instructions, are pregnant, weigh under 50 kg, have contraindications to nerve blocks or take daily pain meds equivalent to more than 60 mg of morphine.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive nerve blocks including the femoral triangle block and potentially additional blocks for postoperative analgesia after knee replacement surgery
Immediate Postoperative Monitoring
Participants are monitored for pain levels, complications, and recovery quality within the first 24 hours after surgery
Follow-up
Participants are monitored for pain intensity, quality of recovery, and patient satisfaction up to 7 days after surgery
What Are the Treatments Tested in This Trial?
Interventions
- Femoral Triangle Block (FTB)
- Infiltration between Popliteal Artery and Capsule of the Knee Block (IPACK)
- Para-Sartorial Compartments (PACS) Block
Find a Clinic Near You
Who Is Running the Clinical Trial?
Centre hospitalier de l'Université de Montréal (CHUM)
Lead Sponsor