search
Back to results

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

Primary Purpose

Total Knee Arthroplasty, Manual Lymphatic Drainage, MLD

Status
Completed
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Manual Lymphatic Drainage
Sponsored by
Moritz Wagner
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Total Knee Arthroplasty

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Total Knee Arthroplasty (TKA)

Exclusion Criteria:

  • Venous insufficiency
  • BMI > 38
  • Vascular disease

Sites / Locations

  • BKH St. Johann in Tirol

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

No Intervention

Experimental

Experimental

Arm Label

Control Group

Manual lymphatic drainage before and after knee replacement

Manual lymphatic drainage after knee replacement

Arm Description

Standard pre- and postoperative physical therapy without manual lymphatic drainage.

Manual lymphatic drainage before and after knee replacement

Manual lymphatic drainage after knee replacement

Outcomes

Primary Outcome Measures

Volume
The swelling/volume is calculated through measurements of the circumference at 7 distinct points of the leg. The unit is [mm].
Function
Knee range of motion (ROM), active and passive. The unit is [degrees]
Knee Pain
Visual analogue scale from 0 to 10 on the average level of knee pain in the last 24 hours.

Secondary Outcome Measures

Subjective patient reported outcome
WOMAC Score (Western Ontario and McMaster University Osteoarthritis Index)

Full Information

First Posted
May 12, 2021
Last Updated
August 1, 2023
Sponsor
Moritz Wagner
Collaborators
Bezirkskrankenhaus St. Johann in Tirol
search

1. Study Identification

Unique Protocol Identification Number
NCT05119764
Brief Title
Manual Lymphatic Drainage Before and After Total Knee Replacement, a Single-center Observer-blinded Randomized Controlled Trial
Official Title
Manual Lymphatic Drainage Before and After Total Knee Replacement, a Single-center Observer-blinded Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Completed
Study Start Date
March 1, 2021 (Actual)
Primary Completion Date
February 1, 2023 (Actual)
Study Completion Date
February 8, 2023 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Moritz Wagner
Collaborators
Bezirkskrankenhaus St. Johann in Tirol

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

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).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Total Knee Arthroplasty, Manual Lymphatic Drainage, MLD, Rehabilitation, Knee Osteoarthritis

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Randomized controlled trial with three treatment groups, two intervention groups and one control group
Masking
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).
Allocation
Randomized
Enrollment
112 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control Group
Arm Type
No Intervention
Arm Description
Standard pre- and postoperative physical therapy without manual lymphatic drainage.
Arm Title
Manual lymphatic drainage before and after knee replacement
Arm Type
Experimental
Arm Description
Manual lymphatic drainage before and after knee replacement
Arm Title
Manual lymphatic drainage after knee replacement
Arm Type
Experimental
Arm Description
Manual lymphatic drainage after knee replacement
Intervention Type
Procedure
Intervention Name(s)
Manual Lymphatic Drainage
Intervention Description
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.
Primary Outcome Measure Information:
Title
Volume
Description
The swelling/volume is calculated through measurements of the circumference at 7 distinct points of the leg. The unit is [mm].
Time Frame
Change in swelling weeks before the operation to one year after the operation
Title
Function
Description
Knee range of motion (ROM), active and passive. The unit is [degrees]
Time Frame
Change in ROM weeks before the operation to one year after the operation
Title
Knee Pain
Description
Visual analogue scale from 0 to 10 on the average level of knee pain in the last 24 hours.
Time Frame
Change in pain weeks before the operation to one year after the operation
Secondary Outcome Measure Information:
Title
Subjective patient reported outcome
Description
WOMAC Score (Western Ontario and McMaster University Osteoarthritis Index)
Time Frame
Before the operation, five days after the operation and one year after the operation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Total Knee Arthroplasty (TKA) Exclusion Criteria: Venous insufficiency BMI > 38 Vascular disease
Facility Information:
Facility Name
BKH St. Johann in Tirol
City
Sankt Johann In Tirol
State/Province
Tyrol
ZIP/Postal Code
6380
Country
Austria

12. IPD Sharing Statement

Plan to Share IPD
Undecided

Learn more about this trial

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

We'll reach out to this number within 24 hrs