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Clinical Trials/NCT01459861
NCT01459861
Terminated
Not Applicable

Assessment of Early Ambulation in Patients Receiving Continuous Adductor Canal Block With Ultrasound Guided Posterior Capsular Knee Injection vs. Femoral Nerve Block With Tibial Nerve Block Following Total Knee Replacement

Trinity Health Of New England1 site in 1 country11 target enrollmentOctober 2011
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ConditionsPainOsteoarthritis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pain
Sponsor
Trinity Health Of New England
Enrollment
11
Locations
1
Primary Endpoint
Ability to ambulate post operatively.
Status
Terminated
Last Updated
13 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSitesSimilar Trials

Overview

Brief Summary

The purpose of this study is to assess early ambulation following total knee replacement in patients receiving continuous adductor canal block with posterior capsular injection compared to continuous femoral nerve block with tibial nerve block.

Registry
clinicaltrials.gov
Start Date
October 2011
End Date
September 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Trinity Health Of New England
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • •knee arthroplasty
  • •ages 18-80

Exclusion Criteria

  • •history of neurological disease
  • •pregnancy
  • •neuropathy
  • •chronic narcotic use
  • •allergy to local anesthetic solution or NSAIDS
  • •inability to give consent or cooperate with the study protocol

Outcomes

Primary Outcomes

Ability to ambulate post operatively.

Time Frame: Up to 3 days (72 hours) post surgery.

Ability to ambulate and perform tasks of the rehabilitation program and reach rehabilitation milestones after total knee arthroplasty.

Secondary Outcomes

  • Pain scores at rest and with knee flexion.(Up to 3 days ( 72 hours) after surgery)
  • Pain Medication Consumption(Up to 3 days (72 hours) post surgery)

Study Sites (1)

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