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Phase 4 N=114 Randomized Single-blind Treatment

Effects of Catheter Location on Postoperative Analgesia for Continuous Adductor Canal and Popliteal-Sciatic Nerve Blocks

Post-surgical Pain · Total Knee Arthroplasty · Foot/Ankle Surgery · Catheterization for Postop Analgesia

Enrolled (actual)
114
Serious AEs
0.0%
Results posted
Sep 2019
Primary outcome: Primary: Pain (Average): Numeric Rating Scale for Pain — 0.5; 3.0 score on a scale

Study Design & Population

Study type
Interventional
Phase
Phase 4
Interventions
ropivacaine 0.2% (Drug)
Age
Adult, Older Adult · 18+ yrs
Sex
All
Sponsor
University of California, San Diego
Primary completion
Feb 2018

Outcome Measures

OutcomeResultp-value
PRIMARY
Pain (Average): Numeric Rating Scale for Pain
0.5; 3.0
SECONDARY
Pain (Worst) :Numeric Rating Scale for Pain
4.0; 5.0
SECONDARY
Analgesic Use: IV Morphine Equivalents
6.7; 6.7
SECONDARY
Ambulation: Distance in Meters
150; 170
SECONDARY
Pain During Afternoon Physical Therapy Session
3.0; 3.0
SECONDARY
Number of Participants That Had Fluid Leakage Reported at Catheter Site.
3; 1
SECONDARY
Toe/Foot Numbness (Insensate) :0-10 Scale
7.0; 7.0
SECONDARY
Total Local Anesthetic Infused (Adductor Only) : mL
32; 40

Summary

Currently, continuous adductor canal and popliteal-sciatic nerve blocks are used commonly for lower extremity post-operative pain control, specifically for total knee arthroplasty and foot/ankle surgery, respectively. A perineural catheter used to infuse local anesthetic for postoperative analgesia may be placed at various locations along the target nerves. Investigations of single-injection peripheral nerve blocks suggest that the onset of the block might be faster with one location over the other; but, the success rates are equivalent. However, remaining unknown is whether there is an optimal location to place a perineural catheter as part of a continuous peripheral nerve block.

Eligibility Criteria

Inclusion Criteria

  • undergoing surgery with an adductor canal or popliteal-sciatic perineural catheter for postoperative analgesia following primary tri-compartment knee arthroplasty or foot/ankle surgery;
  • anticipated to have at least moderate pain following surgery [NRS>3]; and,
  • age 18 years or older.

Exclusion Criteria

  • pregnancy (a urine pregnancy test is standard at UCSD for female patients prior to menopause who are sexually active with the opposite sex within the previous year);
  • inability to communicate with the investigators and hospital staff;
  • clinical neuropathy in the surgical extremity;
  • chronic high-dose opioid use (defined as daily use for more than 4 weeks prior to surgery of at least the equivalent of 20 mg oxycodone);
  • BMI > 40 kg/m2;
  • allergy to study medications (lidocaine, ropivicaine);
  • known renal insufficiency; or,
  • incarceration.
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02523235). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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