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Effect of J-Shaped Incision After Total Knee Arthroplasty (J-TKA)

J-Shaped Incision Reduces Peri-incisional Numbness and Pain After Primary Total Knee Arthroplasty: A Prospective Randomized Controlled Trial

Status
Completed
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07514598
Enrollment
62
Registered
2026-04-07
Start date
2025-09-17
Completion date
2026-05-17
Last updated
2026-05-29

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, Knee Osteoarthritis, J-shaped Incision, Saphenous Nerve, Numbness

Brief summary

This prospective randomized controlled trial evaluates whether a modified J-shaped skin incision can reduce peri-incisional numbness after primary total knee arthroplasty (TKA) compared with the conventional midline skin incision. Peri-incisional numbness is a common postoperative complaint after TKA and is thought to be mainly related to injury of the infrapatellar branch of the saphenous nerve. Although often considered a minor issue, it may adversely affect postoperative comfort, pain perception, and patient satisfaction. A total of 62 patients undergoing primary TKA for Kellgren-Lawrence grade 4 varus knee osteoarthritis were randomized to either a conventional midline incision or a modified J-shaped incision. In the J-shaped technique, the distal part of the incision is curved laterally at the level of the tibial tuberosity in an effort to decrease injury to the infrapatellar branch of the saphenous nerve. The primary outcome is the extent of peri-incisional sensory loss, assessed using Semmes-Weinstein 10-g monofilament testing with a grid-mapping method before surgery and at 2 and 6 months after surgery. Secondary outcomes include pain scores, functional knee scores, range of motion, blood loss, tourniquet time, and wound-related complications.

Detailed description

Total knee arthroplasty is an effective surgical treatment for advanced knee osteoarthritis; however, peri-incisional numbness is a frequent postoperative finding. This sensory disturbance is commonly attributed to injury of the infrapatellar branch of the saphenous nerve during the standard anterior skin incision. Although peri-incisional numbness is often not regarded as a major complication, it may negatively influence postoperative comfort and patient satisfaction and may also be associated with persistent local pain. This study was designed to investigate whether a modified J-shaped skin incision could reduce peri-incisional numbness compared with the conventional midline incision in patients undergoing primary TKA. The underlying rationale is that altering the distal course of the skin incision laterally near the tibial tuberosity may help decrease injury to the infrapatellar branch of the saphenous nerve while preserving standard surgical exposure and not increasing operative difficulty or wound-related complications. In this prospective randomized controlled trial, 62 patients with Kellgren-Lawrence grade 4 varus osteoarthritis scheduled for primary TKA were allocated to one of two groups: a conventional midline incision group or a modified J-shaped incision group. In the modified technique, the distal portion of the incision is curved laterally by approximately 3 cm at the level of the tibial tuberosity. All participants undergo peri-incisional sensory evaluation preoperatively and again at 2 and 6 months postoperatively. Sensory loss is quantified using Semmes-Weinstein 10-g monofilament testing combined with a grid-mapping method to determine the area of numbness. The primary outcome measure is the area of peri-incisional numbness after surgery. Secondary outcome measures include postoperative pain assessed by visual analog scale (VAS), functional outcomes assessed by The Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC), Knee Injury and Osteoarthritis Outcome Score (KOOS), Hospital for Special Surgery Knee-Rating Scale (HSS) and Anterior Knee Pain Scale (AKPS) scores, range of motion, estimated blood loss, tourniquet time, and wound-related complications. These measures are intended to determine whether the modified incision provides sensory and pain-related benefits without adversely affecting clinical recovery, surgical efficiency, or wound healing. Based on the study findings summarized in the abstract, the modified J-shaped incision was associated with a significantly smaller area of postoperative numbness at both 2 and 6 months and with lower pain scores at 6 months, while functional scores, range of motion, blood loss, tourniquet time, and wound-related complications were similar between groups. These findings support the hypothesis that a simple modification of the skin incision may improve postoperative sensory outcomes and comfort after primary TKA without increasing surgical risk.

Interventions

PROCEDUREConventional Midline Incision

A conventional midline skin incision is used during primary total knee arthroplasty.

PROCEDUREJ-shaped Incision

A modified J-shaped skin incision is used during primary total knee arthroplasty, in which the distal portion of the incision is curved laterally at the level of the tibial tuberosity.

Sponsors

Fatih Sultan Mehmet Training and Research Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Masking description

Masking was not feasible due to the visible nature of the surgical incision during postoperative assessments. Therefore, surgeons, participants, and outcome assessors were not blinded to group allocation.

Intervention model description

This is a prospective, randomized, parallel-group study comparing a conventional midline incision with a modified J-shaped incision in patients undergoing primary total knee arthroplasty.

Eligibility

Sex/Gender
ALL
Age
56 Years to 81 Years
Healthy volunteers
No

Inclusion criteria

* Adults undergoing primary total knee arthroplasty * Diagnosis of Kellgren-Lawrence grade 4 varus knee osteoarthritis * Planned treatment with primary total knee arthroplasty * Ability to provide written informed consent * Ability to comply with postoperative follow-up evaluations

Exclusion criteria

* Valgus knee deformity * Revision total knee arthroplasty * Previous surgery on the affected knee * History of periarticular fracture around the knee * Pre-existing sensory deficit or neurologic disorder affecting the operative lower extremity * History of lumbar disc herniation * Known neuromuscular disease * Peripheral vascular disease * Inability to comply with follow-up and postoperative evaluations * Refusal or inability to provide informed consent

Design outcomes

Primary

MeasureTime frameDescription
Area of peri-incisional sensory loss2 months and 6 months postoperativelyThe extent of peri-incisional sensory loss will be assessed using Semmes-Weinstein 10-g monofilament testing combined with a standardized grid-mapping method to quantify the area of numbness around the surgical incision.

Secondary

MeasureTime frameDescription
Postoperative pain2 months and 6 months postoperativelyPostoperative pain will be assessed using the Visual Analog Scale (VAS) for pain at 2 months and 6 months postoperatively. The VAS ranges from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate worse pain.
Range of motion2 months and 6 months postoperativelyKnee range of motion will be measured clinically in degrees.
Intraoperative Blood LossIntraoperative periodIntraoperative blood loss will be recorded during the surgical procedure. Blood loss will be measured in milliliters (mL). Higher values indicate greater blood loss.
Tourniquet TimeIntraoperative periodTourniquet time will be recorded during the surgical procedure. Tourniquet time will be measured in minutes. Higher values indicate longer tourniquet use.
Incision LengthIntraoperative periodIncision length will be measured intraoperatively in centimeters (cm). Higher values indicate a longer skin incision.
Wound complicationsUp to 6 months postoperativelyPostoperative wound-related complications will be assessed clinically.
Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) Score2 months and 6 months postoperativelyFunctional outcome will be assessed using the Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) at 2 months and 6 months postoperatively. If reported on a 0 to 100 scale, 0 indicates the worst symptoms/function and 100 indicates the best symptoms/function. Higher scores indicate better outcome.
Knee injury and Osteoarthritis Outcome Score (KOOS)2 months and 6 months postoperativelyFunctional outcome will be assessed using the Knee injury and Osteoarthritis Outcome Score (KOOS) at 2 months and 6 months postoperatively. KOOS subscale scores range from 0 to 100, where 0 indicates extreme knee problems and 100 indicates no knee problems. Higher scores indicate better outcome.
Hospital for Special Surgery (HSS) Knee Score2 months and 6 months postoperativelyFunctional outcome will be assessed using the Hospital for Special Surgery Knee Score (HSS) at 2 months and 6 months postoperatively. The HSS score ranges from 0 to 100, with higher scores indicating better knee function.
Kujala Anterior Knee Pain Scale Score2 months and 6 months postoperativelyFunctional outcome will be assessed using the Kujala Anterior Knee Pain Scale at 2 months and 6 months postoperatively. The score ranges from 0 to 100, with higher scores indicating better knee function and fewer symptoms.

Countries

Turkey (Türkiye)

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 28, 2026