Continuous Nerve Block for Post-Knee Replacement Pain

Hd
YG
Overseen ByYehoshua Gleicher, MD, MSc
Age: 18+
Sex: Any
Trial Phase: Academic
Sponsor: University of Toronto

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 called continuous adductor canal block (CACB). The researchers aim to determine if this approach offers longer-lasting pain relief and improves recovery compared to a placebo. Individuals undergoing first-time knee replacement surgery who expect to leave the hospital within a day or so might be suitable candidates. The trial will compare the effects of an actual pain relief solution with a placebo to assess effectiveness and safety. As an unphased trial, it provides patients the chance to contribute to innovative pain management research that could enhance recovery experiences for future patients.

Will I have to stop taking my current medications?

The trial information does not specify if you need to stop taking your current medications. However, if you are using chronic opioids equivalent to 30mg of morphine daily, you would not be eligible to participate.

What prior data suggests that continuous adductor canal block is safe for post-knee replacement pain management?

Research has shown that the continuous adductor canal block (CACB) is generally safe for individuals undergoing knee replacement surgery. This pain control method uses a small tube to deliver a steady flow of numbing medicine and is well-tolerated by most patients. Some studies suggest that CACB not only aids in pain relief but also enhances knee movement after surgery.

One study indicated that adductor canal blocks, in general, are safe and effective in reducing pain after knee surgery. This suggests that using them continuously might also be safe, though it requires careful monitoring. While any medical treatment can have side effects, research on CACB has shown that serious issues are rare.

In summary, CACB appears to be a safe option for managing pain after knee replacement, based on current evidence. However, discussing potential risks with a healthcare provider before joining a trial is always advisable.12345

Why are researchers excited about this trial?

Researchers are excited about continuous adductor canal block (CACB) for post-knee replacement pain because it offers a targeted approach that may provide more consistent pain relief compared to traditional pain management methods like opioid medications. Unlike oral painkillers, CACB delivers a local anesthetic, ropivacaine, directly to the adductor canal, potentially reducing systemic side effects and the risk of opioid dependency. This localized delivery could lead to quicker recovery times and better mobility after surgery, making it a promising alternative for enhancing post-operative care.

What evidence suggests that continuous adductor canal block is effective for post-knee replacement pain?

Research shows that a continuous adductor canal block (CACB), which participants in this trial may receive, can effectively manage pain after knee replacement surgery. Studies have found that CACB significantly reduces pain and the need for additional pain medication. For instance, one study discovered that patients using CACB required fewer opioids, which are strong painkillers, compared to those who received a sham continuous adductor canal block (ShACB), the placebo treatment in this trial. Another study demonstrated that patients had better muscle strength after surgery when using CACB. Overall, CACB helps patients recover more comfortably and effectively after knee surgery.14678

Who Is on the Research Team?

NS

Naveed Siddiqui, MD, MSc

Principal Investigator

University of Toronto

Are You a Good Fit for This Trial?

This trial is for patients over 21 years old who are having knee replacement surgery as outpatients and have a moderate risk of complications (ASA I-III). They should not be dependent on alcohol or drugs, understand the treatment process, and cannot be using strong painkillers regularly. People with allergies to study meds, blood clotting issues, low platelet counts, or problems where the catheter goes can't join.

Inclusion Criteria

I am older than 21 years.
My overall health is good to moderately impaired.
You don't have a problem with drinking too much alcohol or using drugs.
See 2 more

Exclusion Criteria

I was admitted to the hospital due to complications after surgery.
Your blood doesn't clot properly and your platelet count is too low.
I have been using opioids equivalent to 30mg of morphine daily for the past 2 weeks.
See 2 more

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks
1 visit (in-person)

Pre-surgery Assessment

Pre anesthesia consult and study explanation, including consent form review

At least 2 days
1 visit (in-person)

Treatment

Patients undergo total knee arthroplasty with continuous adductor canal block or sham block

60 hours
1 visit (in-person)

Follow-up

Participants are monitored for catheter associated complications and quality of recovery

30 days
Phone follow-ups on Days 1, 2, 3, and 30

What Are the Treatments Tested in This Trial?

Interventions

  • Continuous adductor canal block (CACB)
  • Sham continuous adductor canal block (ShACB)
Trial Overview The study tests if continuous adductor canal block (CACB), which involves infusing pain medication through a tube near nerves in the thigh, provides better pain control and recovery after outpatient knee surgery compared to a sham procedure without real medicine (ShACB).
How Is the Trial Designed?
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Continuous adductor canal block (CACB)Experimental Treatment1 Intervention
Group II: Sham continuous adductor canal block (ShACB).Placebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

University of Toronto

Lead Sponsor

Trials
739
Recruited
1,125,000+

MOUNT SINAI HOSPITAL

Collaborator

Trials
44
Recruited
17,000+

Published Research Related to This Trial

In a study of 145 patients undergoing total knee arthroplasty, continuous adductor canal blocks (CACB) resulted in better ambulation and lower pain scores compared to epidural analgesia, indicating enhanced postoperative recovery.
Patients receiving CACB reported higher satisfaction rates (68% in general + CACB and 63% in spinal + CACB) compared to those receiving combined spinal-epidural analgesia (36%), suggesting that CACB may be a more favorable option for pain management in knee surgery.
Continuous Adductor Canal Blocks Provide Superior Ambulation and Pain Control Compared to Epidural Analgesia for Primary Knee Arthroplasty: A Randomized, Controlled Trial.Kayupov, E., Okroj, K., Young, AC., et al.[2022]
In a study of 57 total knee arthroplasty patients, both proximal and distal adductor canal blocks (ACBs) provided similar levels of postoperative pain relief, as indicated by comparable opioid consumption and pain scores.
While the proximal ACB group showed a trend towards better functional mobility (measured by the 'Up and Go' test), this difference was not statistically significant, suggesting that both techniques are equally effective for pain management post-surgery.
A Randomized Comparison of Pain Control and Functional Mobility between Proximal and Distal Adductor Canal Blocks for Total Knee Replacement.Romano, C., Lloyd, A., Nair, S., et al.[2022]
In a study of 120 patients undergoing total knee arthroplasty, the combination of adductor canal block (ACB) and interspace between popliteal artery and capsule of posterior knee block (IPACK) provided significantly better pain relief compared to ACB alone, as measured by VAS scores.
Patients receiving the ACB+IPACK technique also demonstrated improved range of motion and ambulation distance post-surgery, indicating that this method enhances recovery without compromising motor function.
Comparison of adductor canal block and IPACK block (interspace between the popliteal artery and the capsule of the posterior knee) with adductor canal block alone after total knee arthroplasty: a prospective control trial on pain and knee function in immediate postoperative period.Sankineani, SR., Reddy, ARC., Eachempati, KK., et al.[2022]

Citations

Effectiveness of continuous adductor canal block versus ...The muscle strength of patients in the CACB group post-operation was significantly improved than those of the CFNB group (SMD = 0.81; 95% CI: 0.35, 1.26; P = .
The effects of continuous catheter adductor canal block for ...It is anticipated that CACB will be more effective in reducing postoperative pain than SACB, leading to decreased rescue analgesia usage and ...
Outpatient continuous adductor canal block (CACB) for ...Conclusions In our study, CACB significantly enhanced early postoperative recovery and analgesia following TKA in an outpatient or short-stay ...
Postoperative continuous adductor canal block for total ...Conclusion. A postoperative cACB after total knee arthroplasty significantly reduces total opioid consumption and pain scores compared to sham catheter.
The analgesic effect of continuous adductor canal block ...The results showed that PPB could effectively improve maximum pain in the posterior knee at least within 12 h after TKA. Meanwhile, the addition ...
Analgesic Efficacy of Adductor Canal Block in Total Knee ...The aim of this meta‐analysis and systematic review of randomized controlled trials (RCTs) was to evaluate the efficacy and safety of adductor canal block ...
Continuous Adductor Canal Block in Outpatient Total Knee ...Objectives: Evaluate effectiveness and safety of using continuous adductor canal block (CACB) in patients undergoing primary total knee arthroplasty (TKA), in ...
Adductor canal block in total knee arthroplasty: a scoping ...Adductor canal block is a safe and potentially effective peripheral nerve block for reducing postoperative pain after total knee arthroplasty while preserving ...
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