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

F

Fatih Sultan Mehmet Training and Research Hospital

Status

Completed

Conditions

Osteoarthritis, Knee

Treatments

Procedure: Conventional Midline Incision
Procedure: J-shaped Incision

Study type

Interventional

Funder types

Other

Identifiers

NCT07514598
J-TKA-2026

Details and patient eligibility

About

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.

Full 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.

Enrollment

62 patients

Sex

All

Ages

56 to 81 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

62 participants in 2 patient groups

Midline Incision
Active Comparator group
Description:
Participants undergo primary total knee arthroplasty using a conventional midline skin incision.
Treatment:
Procedure: Conventional Midline Incision
J-shaped Incision
Experimental group
Description:
Participants undergo primary total knee arthroplasty using a modified J-shaped skin incision, in which the distal portion of the incision is curved laterally at the level of the tibial tuberosity.
Treatment:
Procedure: J-shaped Incision

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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