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Clinical Trials/NCT02360735
NCT02360735
Terminated
Not Applicable

Manual Lymph Drainage for Patients With Acute Total Knee Replacement

Anne Arundel Health System Research Institute1 site in 1 country4 target enrollmentJanuary 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Total Knee Arthroplasty
Sponsor
Anne Arundel Health System Research Institute
Enrollment
4
Locations
1
Primary Endpoint
Range of Motion
Status
Terminated
Last Updated
8 years ago

Overview

Brief Summary

Manual Lymphatic Drainage (MLD) is a specialized massage technique utilized to decrease various forms of edema. This technique promotes reuptake of interstitial fluid along the pathways of the lymphatic system. This technique promotes healing, decrease swelling, and decrease pain.

Detailed Description

Manual Lymphatic Drainage (MLD) is a specialized massage technique utilized to decrease various forms of edema. Edema can limit function, range of motion (ROM) and increase pain after surgery. Studies have shown that decreasing edema can increase knee strength and functional performance on various standardized measures. MLD has been shown to be effective in patients with hind foot operations and increases ROM post total knee replacement (TKR) surgery. The aim of this study is to determine whether MLD on a sample of patients with TKR will decrease edema, increase ROM and decrease pain as compared to TKR patients who do not receive MLD.

Registry
clinicaltrials.gov
Start Date
January 2015
End Date
October 11, 2016
Last Updated
8 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Anne Arundel Health System Research Institute
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • s/p total knee replacement
  • Primary diagnosis of osteoarthritis or degenerative joint disease
  • Able to read and understand English to consent
  • Acceptance of the study protocol procedure

Exclusion Criteria

  • Active infection
  • Metastatic or systemic malignancy
  • Acute thrombus
  • History of pulmonary embolism
  • Major cardiac pathology such has angina
  • Heart attack or uncompensated congestive heart failure (CHF)
  • Body mass index (BMI) \> 40
  • Pregnant or lactating women
  • Renal dysfunction
  • Joint revision

Outcomes

Primary Outcomes

Range of Motion

Time Frame: 3 days

Determine if performing MLD after TKR surgery increases range of motion as compared to the standard of care

Girth

Time Frame: 3 days

Determine if performing MLD after TKR surgery decreases girth and swelling in the knee as compared to the standar of care

Pain Scores

Time Frame: 3 days

Determine if performing MLD after TKR surgery decreases pain in the knee as compared to controls

Study Sites (1)

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