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Does Electrocautery Increase Postoperative Pain in Primary Total Knee Arthroplasty

Does Electrocautery Increase Postoperative Pain in Primary Total Knee Arthroplasty: A Randomized Controlled Trial

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06239038
Enrollment
132
Registered
2024-02-02
Start date
2021-10-11
Completion date
2024-02-29
Last updated
2024-02-06

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

Conditions

Osteoarthritis, Knee

Keywords

Total knee arthroplasty, Electrocautery, Scalpel, Post-operative pain, Pain score

Brief summary

Total knee arthroplasty (TKA) is a successful treatment for end-stage osteoarthritis of the knee. The main advantages of TKA are to relieve the pain of the knee, improve the knee function, restore lower limb alignment, and improve the quality of life for patients. During TKA, some surgeons prefer using a scalpel while others using electrocautery to expose the articular cavity. Whether the use of scalpel can lead to better and faster recovery after the primary TKA is still controversial. The aim of this study was to compare the clinical outcomes of using the scalpel and the electrocautery in primary TKA

Detailed description

A randomized controlled trial of patients underwent primary TKA between October 2021 and October 2023. The groups will be determined by using the computer to generate a randomization lists. A total 132 patients were included with 66 patients in the scalpel group, 66 patients in the electrocautery group. All patients were evaluated using primary outcome : Post-operative Visual Analog Scale (VAS) of pain, secondary outcome: estimated blood loss and Knee Injury and Osteoarthritis Outcome Score (KOOS-JR)

Interventions

PROCEDUREtotal knee arthroplasty

total knee arthroplasty surgery with Police Arthroplasty joint academy center(PAJAC) Subvastus Approach

Sponsors

Police General Hospital, Thailand
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Intervention model description

In electrocautery group, using an electrocautery in following step 1. Stop bleeding at subcutaneous tissue layer 2. Remove anterior cruciate ligament and posterior cruciate ligament 3. Bony mark for further bone cut 4. Patellar denervation 5. Soft tissue removal 6. Synovial tissue removal In scalpel group, proceed with following step 1. Using electrocautery for stop bleeding at subcutaneous tissue layer 2. In deep layer still use scalpel for Remove anterior cruciate ligament and posterior cruciate ligament 3. Soft tissue removal and synovial tissue removal 4. No patellar denervation

Eligibility

Sex/Gender
ALL
Age
58 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Osteoarthritis patient (KL classification gr 2-4) * Primary TKA * Varus deformity \< 20 degree * Flexion contracture \< 20 degree

Exclusion criteria

* Coagulopathy * Platelet dysfunction * Inflammatory arthritis * Revision TKA

Design outcomes

Primary

MeasureTime frameDescription
Postoperative pain (visual analog scale) day 1-4postoperative day 1-4measure the Postoperative pain by using visual analog scale from 1 - 10, higher scores means worse outcome

Secondary

MeasureTime frameDescription
Calculated blood losspostoperative day 4Calculated blood loss using Mercuruali's formula
Functional scorefollow up 2 weeks, 1,3,6 monthsFunctional score using KOOS JR score, range from 0 to 100 with a score of 0 indicating total knee disability and 100 indicating perfect knee health

Countries

Thailand

Outcome results

None listed

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