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Photobiomodulation Therapy in Patients Receiving Total Knee Arthroplasty

A Randomized Trial of Photobiomodulation Effect in Patients Receiving Total Knee Arthroplasty

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06426251
Enrollment
15
Registered
2024-05-23
Start date
2024-05-20
Completion date
2027-12-31
Last updated
2024-05-29

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

Conditions

Inflammation, Osteoarthritis, Post Operative Pain

Brief summary

Photobiomdoulation is the use of near-infrared light to relieve pain, stimulate healing and reduce inflammation. Swelling and inflammation is a common condition after orthopedics surgeries over extremity and spine. This study aim to evaluate the effect of photobiomodulation over patients after Total Knee Arthroplasty.

Detailed description

Patients aged over 20 after Total Knee Arthroplasty in our institution would be candidate for recruitment. The patients will be randomized to receive routine post operative care or photobiomodulation therapy. The swelling extent and subjective outcome will be recorded.

Interventions

DEVICEPhotobiomodulation

Photobiomodulation therapy will be given daily start on the first day after surgery to post operative day 6

Sponsors

National Taiwan University Hospital Hsin-Chu Branch
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

* total knee arthroplasty

Exclusion criteria

* open injury * pregnancy * wound without primary closure * infection * previous surgery over surgical site * skin defect

Design outcomes

Primary

MeasureTime frameDescription
the change of bioimpedancethe bioimpedance measured once daily since post operative day1 to day6 and at 2 weeksbioimpedance of the surgical site will be measured for evaluation of swelling change

Secondary

MeasureTime frameDescription
pain score (visual analogue score)once daily since post operative day1 to day6patient reported pain score, from 0 to 100 points
active range of motion of kneeonce daily since post operative day1 to day6active range of motion of knee
2 minute walk testonce daily since post operative day1 to day6the distance that the patient could walk within 2 minutes

Countries

Taiwan

Contacts

Primary ContactHsiang-Chieh Hsieh
thungjay2@gmail.com886972654075

Outcome results

None listed

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