Effect of Patellar Denervation on Post-operative Knee Pain and Knee Function in Total Knee Arthroplasty
PD
1 other identifier
interventional
64
1 country
1
Brief Summary
This study is a double-blind randomized controlled trial aiming to investigate the effects of patellar denervation using electrocautery on postoperative knee pain and knee function in patients undergoing primary total knee arthroplasty (TKA) without patellar resurfacing.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Aug 2023
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
August 8, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
June 21, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
June 21, 2025
CompletedFirst Submitted
Initial submission to the registry
December 25, 2025
CompletedFirst Posted
Study publicly available on registry
January 15, 2026
CompletedJanuary 15, 2026
January 1, 2026
1.9 years
December 25, 2025
January 7, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Visual analog scale score for knee pain
2 weeks, 6 weeks, 3 months, 6 months, and 12 months
Secondary Outcomes (3)
Kujala score
3 months, 1 year
Knee Society score
3 months, 1 year
Timed up and go test
3 months, 1 year
Study Arms (2)
Patellar Denervation
EXPERIMENTALNon-Patellar Denervation
NO INTERVENTIONInterventions
Electrocautery patella circumferentially during total knee arthroplasty
Eligibility Criteria
You may qualify if:
- Age 55-85 years old
- Knee osteoarthritis
- Plan for total knee arthroplasty after failed conservative treatment for at least 3 months
You may not qualify if:
- Previous history of trauma, fracture or open surgery on the same knee
- Inflammatory arthritis or Crystal-induced arthritis
- Patellar instability or isolated patellofemoral osteoarthritis
- Unable to answer questionnaire
- Cannot tolerate surgery due to medical comorbidities
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Chalathorn Kulthonchalanan
Chon Buri, Changwat Chon Buri, 20110, Thailand
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- TRIPLE
- Who Masked
- PARTICIPANT, INVESTIGATOR, OUTCOMES ASSESSOR
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 25, 2025
First Posted
January 15, 2026
Study Start
August 8, 2023
Primary Completion
June 21, 2025
Study Completion
June 21, 2025
Last Updated
January 15, 2026
Record last verified: 2026-01
Data Sharing
- IPD Sharing
- Will not share
Data was save in form of Google sheet