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Manual Lymph Drainage

Manual Lymph Drainage for Patients With Acute Total Knee Replacement

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02360735
Acronym
MLD
Enrollment
4
Registered
2015-02-11
Start date
2015-01-31
Completion date
2016-10-11
Last updated
2018-01-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Post-operative Edema, Total Knee Arthroplasty

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.

Interventions

OTHERManual Lymphatic Drainage

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.

OTHERPhysical Therapy

All patients will participate in joint physical therapy classes during their inpatient stay.

Sponsors

Anne Arundel Health System Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
45 Years to 90 Years
Healthy volunteers
No

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 * Tumor * 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 * Hospitalization length of stay less than or greater than 3 days * Previous knee replacement * Bilateral knee replacement

Design outcomes

Primary

MeasureTime frameDescription
Pain Scores3 daysDetermine if performing MLD after TKR surgery decreases pain in the knee as compared to controls
Range of Motion3 daysDetermine if performing MLD after TKR surgery increases range of motion as compared to the standard of care
Girth3 daysDetermine if performing MLD after TKR surgery decreases girth and swelling in the knee as compared to the standar of care

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026