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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 16 December 2017
Main ID:  NCT02701114
Date of registration: 29/02/2016
Prospective Registration: No
Primary sponsor: Benaroya Research Institute
Public title: Proximal Versus Distal Adductor Canal Blocks for Total Knee Arthroplasty
Scientific title: A Comparison of Proximal Versus Distal Continuous Adductor Canal Blocks After Total Knee Arthroplasty
Date of first enrolment: February 2016
Target sample size: 76
Recruitment status: Completed
URL:  https://clinicaltrials.gov/show/NCT02701114
Study type:  Interventional
Study design:  Allocation: Randomized. Intervention model: Parallel Assignment. Primary purpose: Treatment. Masking: Double (Participant, Outcomes Assessor).  
Phase:  N/A
Countries of recruitment
United States
Contacts
Name:     Neil A Hanson, MD
Address: 
Telephone:
Email:
Affiliation:  Virginia Mason Medical Center
Key inclusion & exclusion criteria

Inclusion Criteria:

- Unilateral Total Knee Arthroplasty

- ASA physical status I-III

- >18 years old

- Non-pregnant

- Consent to participate in the study

Exclusion Criteria:

- Refusal to participate

- <18 years old

- Chronic opioid use

- Localized infection Pregnancy Pre-existing coagulopathy Allergy to ultrasound gel or
local anesthetics Contraindication to or refusal of spinal anesthetic



Age minimum: 18 Years
Age maximum: N/A
Gender: All
Health Condition(s) or Problem(s) studied
Post-Operative Pain
Intervention(s)
Procedure: Distal Adductor Canal Block
Procedure: Proximal Adductor Canal Block
Primary Outcome(s)
Opioid Consumption (IV Morphine Equivalents) [Time Frame: 24 Hours]
Secondary Outcome(s)
Pain (Numeric Rating) [Time Frame: 48 Hours]
Quadriceps Strength (% of Baseline) [Time Frame: 48 Hours]
Distance Ambulated (Feet) [Time Frame: 48 Hours]
Opioid Consumption (IV Morphine Equivalents) [Time Frame: 48 Hours]
Secondary ID(s)
IRB15118
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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