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Manual Lymphatic Drainage Before and After Total Knee Replacement, a Single-center Observer-blinded Randomized Controlled Trial

Manual Lymphatic Drainage Before and After Total Knee Replacement, a Single-center Observer-blinded Randomized Controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05119764
Enrollment
112
Registered
2021-11-15
Start date
2021-03-01
Completion date
2023-02-08
Last updated
2023-08-02

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

Conditions

Knee Osteoarthritis, Manual Lymphatic Drainage, MLD, Rehabilitation, Total Knee Arthroplasty

Brief summary

The aim of this observer-blinded randomized controlled trial is the evaluation of the influence of manual lymphatic drainage (MLD) on the outcome of patients receiving total knee replacement (TKA).

Interventions

PROCEDUREManual Lymphatic Drainage

Manual Lymphatic Drainage is a form of physical therapy with the primary goal of accelerating lymphatic drainage. In this study, the manual lymphatic drainage is applied by experienced physical therapists 5 days in a row for 30 minutes each; after and/or before the surgery.

Sponsors

Bezirkskrankenhaus St. Johann in Tirol
CollaboratorOTHER
Moritz Wagner
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Investigator)

Masking description

Observer/Investigators are unaware of the treatment arm of each patient. Patients cannot be blinded, due to the obvious treatment intervention (manual lymphatic drainage 15 minutes for 5 days).

Intervention model description

Randomized controlled trial with three treatment groups, two intervention groups and one control group

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Total Knee Arthroplasty (TKA)

Exclusion criteria

* Venous insufficiency * BMI \> 38 * Vascular disease

Design outcomes

Primary

MeasureTime frameDescription
VolumeChange in swelling weeks before the operation to one year after the operationThe swelling/volume is calculated through measurements of the circumference at 7 distinct points of the leg. The unit is \[mm\].
FunctionChange in ROM weeks before the operation to one year after the operationKnee range of motion (ROM), active and passive. The unit is \[degrees\]
Knee PainChange in pain weeks before the operation to one year after the operationVisual analogue scale from 0 to 10 on the average level of knee pain in the last 24 hours.

Secondary

MeasureTime frameDescription
Subjective patient reported outcomeBefore the operation, five days after the operation and one year after the operationWOMAC Score (Western Ontario and McMaster University Osteoarthritis Index)

Countries

Austria

Outcome results

None listed

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