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N/A Completed N=80 Randomized Double-blind Treatment

Posterior Capsular Injection With Femoral Nerve Block for Total Knee Arthroplasty

Posterior Knee Infiltration
Source: ClinicalTrials.gov NCT02701296 ↗
Enrolled (actual)
80
Serious AEs
0.0%
Results posted
Jun 2017
Primary outcomePrimary: Pain Intensity — 3.5; 3.2; 2.1; 1.5 pain score

Summary

To assess pain control after total knee replacement surgery using two different nerve block techniques. The 2 methods are: 1. Continuous femoral nerve block with ultrasound guided posterior capsular injection 2. Continuous femoral nerve block with ultrasound selective tibial nerve block.

Outcome Measures

OutcomeResultp-value
PRIMARY
Pain Intensity
3.5; 3.2; 2.1; 1.5; 1.9; 2.0
SECONDARY
Opioid Consumption
0.33; 0.42
SECONDARY
Plantar Flexion in the Tibial Nerve Distribution
1; 0; 3; 25; 38; 11
SECONDARY
Cold Sensation in the Tibial Nerve Distribution
1; 6; 7; 27; 34; 3
SECONDARY
Dorsiflexion in the Peroneal Nerve Distribution
0; 0; 1; 4; 41; 32
SECONDARY
Sensation in the Peroneal Nerve Distribution
2; 1; 3; 11; 37; 24

Eligibility Criteria

Inclusion Criteria

  • Patients having primary, unilateral total knee arthroplasty
  • Age 18-80

Exclusion Criteria

  • History of neurologic disease, neuropathy, diabetes, or major systemic illness
  • Allergy to local anesthetic solution or NSAIDs
  • Pregnancy
  • Chronic use of narcotics
  • Inability to give consent/cooperate with study
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT02701296). 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. Informational only — not medical advice.

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