Nerve Block Techniques for Postoperative Pain from Knee Surgery

JD
MR
JD
Overseen ByJulie Desroches, Ph. D
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: Centre hospitalier de l'Université de Montréal (CHUM)
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)
Approved in 1 JurisdictionThis treatment is already approved in other countries

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.12345

Why 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?

MR

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

Your health condition falls within the categories 1 to 3 according to the American Society of Anesthesiologists classification.

Exclusion Criteria

I take more than 60 mg of morphine daily for chronic pain.
I weigh less than 50 kg.
I cannot have a peripheral nerve block due to health reasons.
See 4 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive nerve blocks including the femoral triangle block and potentially additional blocks for postoperative analgesia after knee replacement surgery

1 day
1 visit (in-person)

Immediate Postoperative Monitoring

Participants are monitored for pain levels, complications, and recovery quality within the first 24 hours after surgery

24 hours
Continuous monitoring

Follow-up

Participants are monitored for pain intensity, quality of recovery, and patient satisfaction up to 7 days after surgery

7 days

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
Trial Overview The study tests if adding a para-sartorial compartments (PACS) block to the femoral triangle block (FTB) improves pain relief after knee replacement surgery. The PACS aims at blocking additional nerves that aren't covered by FTB alone and could enhance postoperative analgesia allowing earlier mobilization.
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Active Control
Group I: Para-Sartorial Compartment (PACS) Block + Femoral Triangle Block (FTB) + IPACK blockExperimental Treatment3 Interventions
Group II: Femoral Triangle Block (FTB) + IPACK blockActive Control2 Interventions

Find a Clinic Near You

Who Is Running the Clinical Trial?

Centre hospitalier de l'Université de Montréal (CHUM)

Lead Sponsor

Trials
389
Recruited
143,000+

Published Research Related to This Trial

Femoral nerve block significantly improves postoperative pain management after outpatient anterior cruciate ligament repair, with patients receiving a sham block reporting higher pain scores and needing more intravenous analgesia.
Both 0.25% and 0.5% bupivacaine provided effective analgesia lasting approximately 23.2 and 25.7 hours, respectively, demonstrating that femoral nerve blocks can enhance recovery in the immediate postoperative period.
Femoral nerve block with 0.25% or 0.5% bupivacaine improves postoperative analgesia following outpatient arthroscopic anterior cruciate ligament repair.Mulroy, MF., Larkin, KL., Batra, MS., et al.[2022]
In a study of 78 patients undergoing total knee arthroplasty, the combination of an obturator nerve block (ONB) and a femoral triangle block (FTB) significantly reduced opioid consumption to just 2 mg in the first 24 hours, compared to 20 mg for FTB alone and 17 mg for local infiltration analgesia (LIA).
Patients receiving the combined ONB and FTB also experienced less pain, nausea, and vomiting, indicating improved postoperative comfort without negatively affecting their ability to ambulate.
The Analgesic Effect of Obturator Nerve Block Added to a Femoral Triangle Block After Total Knee Arthroplasty: A Randomized Controlled Trial.Runge, C., Børglum, J., Jensen, JM., et al.[2019]
In a study of 80 patients undergoing total knee arthroplasty, combining an anterior femoral cutaneous nerve block (AFCNB) with a femoral triangle block (FTB) significantly reduced pain during movement 12 hours post-surgery compared to FTB alone, with a mean difference in pain scores of -2.02.
The AFCNB + FTB group also experienced lower incidence of surgical site pain and reduced morphine consumption within 48 hours postoperatively, while showing improved quadriceps muscle strength immediately after surgery.
The analgesic efficacy of anterior femoral cutaneous nerve block in combination with femoral triangle block in total knee arthroplasty: a randomized controlled trial.Kampitak, W., Tanavalee, A., Tansatit, T., et al.[2022]

Citations

1.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/34039734/
Combination of femoral triangle block and infiltration ...Recently, the iPACK block (infiltration between the popliteal artery and the capsule of the posterior knee) has been described to relieve posterior knee pain.
Para-sartorial Compartment Block in Knee SurgeryParasartorial compartment block (PSKB); is based on the blockade of the branches of the saphenous nerve, the two largest sensory nerves from the femoral nerve ...
The para‐sartorial compartments (PASC) blockFor posterior compartment pain relief, the infiltration between the popliteal artery and the knee capsule is the preferred approach.
4.pubmed.ncbi.nlm.nih.govpubmed.ncbi.nlm.nih.gov/35144303/
Comparison of Femoral Triangle Block in Combination with ...Combining FTB and IPACK significantly increased the quadriceps muscle in patients, together with relieving early pain and reducing the amount of anesthetic ...
Fascial plane blocks for postoperative pain management...This narrative review evaluates the effectiveness and safety of motor-sparing fascial plane blocks for total knee replacement
Implementation of the IPACK (Infiltration between ...The Infiltration between the Popliteal Artery and Capsule of the Knee (IPACK) block is a new anesthesiologist- administered analgesic technique for ...
Para-sartorial compartments (Pasc) block for knee surgeries[5] Moreover, a recent study advocated blocking the intermediate femoral cutaneous nerve (IFCN) separately using triple injection ...
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