Skip to content

Anteroposterior glide versus rotating platform low contact stress knee arthroplasty

Anteroposterior glide versus rotating platform low contact stress knee arthroplasty

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN52943804
Enrollment
50
Registered
2007-01-05
Start date
2004-10-20
Completion date
Unknown
Last updated
2018-09-10

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

Conditions

Osteoarthritis Musculoskeletal Diseases Arthitis

Interventions

1. Study and compare the improvement in knee motion and overall function after AP glide and rotating platform design LCS knee arthroplasty. 2. Examine the effect of this intervention on proprioception

Sponsors

University Hospital of North Staffordshire NHS Trust (UK)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Patients require a primary bi- or tri- compartmental knee replacement 2. Patients require unilateral knee replacement 3. Patients have given their voluntary, written informed consent

Exclusion criteria

Exclusion criteria: 1. Patients are going to have revision knee surgery 2. Patients are scheduled to have bilateral knee replacement in one sitting 3. Patients suffer from rheumatoid arthritis, diabetes mellitus, post-traumatic arthritis or any form of neurological disorder that can affect the joint position sense 4. Patients have had or will require a major knee arthrotomy on the other same side within six months period 5. Patients have more than 20 degrees of varus, valgus or flexion deformity

Design outcomes

Primary

MeasureTime frame
The primary outcome measure for this study will be the improvement in knee motion (as measured by FASTRAK system). This will be done before operation and at three and six months after the operation at bionic laboratory at Hartshill Orthopaedic Surgical Unit.

Secondary

MeasureTime frame
1. Proprioception as measured by absolute error angle (this is the difference between actual and perceived angle through which the joint has been moved passively). 2. American knee society score, oxford knee score, EuroQol instrument and the Short Form health survey (SF12) will be recorded before and at three months after the operation. 3. Complications 4. Statistical considerations

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026