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Randomized controlled trial about the lymph drainage intervention in the physiotherapy after the total knee arthroplasty

Randomized controlled trial about the lymph drainage intervention in the physiotherapy after the total knee arthroplasty - RCT examination about the lymph drainage intervention after the total knee replacement

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000020540
Enrollment
50
Registered
2016-01-13
Start date
2016-01-07
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

knee osteoarthritis

Interventions

The intervention group does it in addition to the normal physiotherapy of approximately 40 minutes with a group giving the lymph drainage of 20 minutes. I do it after an operation after an operation u

Sponsors

yokohama city university medical center
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1)The age at registration is a patient younger than 85 years 45 years old or older (2)The patient who agreed to osteoarthrosis being diagnosed, and doing total knee arthroplasty (3)The patient who has not been for the joint by total knee arthroplasty so far. (4)The patient who plans unilateral total knee arthroplasty. (5)The patient who was able to perform intervention of the physical therapy before operation. (6)The patient that an answer to questionary survey is possible. (7)The patient that an agreement is provided in a document about the participation of this study.

Exclusion criteria

Exclusion criteria: (1)It is a patient with the past with deep vein thrombosis or heart failure. (2)Under 45 years old, patient 85 years or older (3)The patient who receives total knee arthroplasty at the both sides same time. (4)Severe cognitive functional decline and patient with a mental disorder. (5)In addition, the patient whom it was judged the judgment of the doctor to be inappropriate as an object.

Design outcomes

Primary

MeasureTime frame
pain of about the tenth day after surgery

Secondary

MeasureTime frame
circumference,muscle strength,maximum gait velocity

Countries

Japan

Contacts

Public ContactTatsu Fujiura

yokohama city university medical center rehabilitation division

tatsufujiura@gmail.com045-261-5656

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026