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A Comparison of Kneeling Ability After Lateral or Midline Incisions In Total Knee Arthroplasty

A Comparison of Kneeling Ability After Lateral or Midline Incisions In Total Knee Arthroplasty

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12621001115820
Enrollment
0
Registered
2021-08-23
Start date
2024-12-05
Completion date
2025-12-30
Last updated
2025-01-06

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

Conditions

None listed

Brief summary

This is a prospective randomized controlled trial comparing the outcome of patients undergoing primary total knee arthroplasty with either a midline or a lateral skin incision. Patient outcomes will be collected and compared between the two surgical cohorts over a 24 month post-operative period, and will include a range of subjective and functional outcomes, and kneeling tolerance. It is hypothesised that there will be no difference in kneeling tolerance between midline or lateral skin incisions.

Interventions

Patients will be randomised to receive either a midline skin incision or a lateral skin incision. All patients will undergo total knee arthroplasty via a medial parapatellar approach. Total knee arthroplasty will take from 60 to 90 minutes, surgical duration, across all groups. Within the group of treating surgeons there will also be a distribution of patients receiving a total knee arthroplasty via navigated and non-navigated techniques, and receiving cruciate retaining or cruciate sacrificing

Patients will be randomised to receive either a midline skin incision or a lateral skin incision. All patients will undergo total knee arthroplasty via a medial parapatellar approach. Total knee arthroplasty will take from 60 to 90 minutes, surgical duration, across all groups. Within the group of treating surgeons there will also be a distribution of patients receiving a total knee arthroplasty via navigated and non-navigated techniques, and receiving cruciate retaining or cruciate sacrificing knee replacements as per the surgeons’ preferred practice. These will not be specifically controlled for in the randomisation process as they are unlikely to affect kneeling tolerance and doing so will limit the external validity of the trial. Randomisation will be stratified based on patella resurfacing or no patella resurfacing, as this may impact kneeling tolerance. Adherence to the randomisation schedule will be monitored by audit of the operation notes. Post-operatively, all participants will undergo routine rehabilitation for total knee arthroplasty, involving full weight bearing and early active range of movement. Post-operative analgesia will consist of paracetamol and non-steroidal anti-inflammatories, with opioids for breakthrough pain as per routine clinical treatment.

Sponsors

Perth Orthopaedic and Sports Medicine Centre
Lead SponsorOther

Study design

Allocation
Randomised controlled trial
Intervention model
Parallel
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

- Age > 18 years - Primary TKA (including bilateral) - Undergoing a medial arthrotomy - Not currently being treated for a psychiatric disorder, senile dementia, Alzheimer’s disease, presence of alcohol/substance abuse.

Exclusion criteria

- Revision TKA (i.e. not primary surgery) - Existing contralateral TKA with <110 degrees of flexion movement - Poorly controlled diabetes or peripheral vascular disease - Range of motion of 90 degrees or less pre-operatively - Peripheral neuropathy or previous history of major spinal surgery - Previous medial incision around the knee joint longer than 5 cm - Previous major knee surgery (e.g. tibial tubercle transfer, tibial plateau fracture or open meniscus resection etc.)

Outcome results

None listed

Source: ANZCTR · Data processed: Feb 4, 2026