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A Study to Determine the Performance of the Press Fit Condylar (P.F.C.) Sigma RP-F Knee System

Phase 4
Terminated
Conditions
Osteoarthritis
Interventions
Device: P.F.C. Sigma RP-F Total Knee Replacement
Registration Number
NCT00761410
Lead Sponsor
DePuy International
Brief Summary

The purpose of this study is to evaluate if the P.F.C. Sigma RPF knee accommodates functional stability with a post-operative passive range of motion of greater than 125° of flexion and to demonstrate that the range of motion does not compromise the longevity of the implant.

Detailed Description

Primary endpoint is to demonstrate that 90% of patients have a functionally stable knee that can achieve post operative range of motion of 125 degrees or greater.

The secondary endpoint is to investigate the survivorship of the P.F.C. Sigma RP-F knee at 1, 2, 3, 5, 10, 15 and 20 years

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
170
Inclusion Criteria
  • Male or female subjects, aged between 45 and 75 years inclusive.
  • Subjects who are able to give voluntary, written informed consent to participate in this investigation and from whom consent has been obtained.
  • Subjects who are able to achieve a pre-operative passive range of motion of equal to or greater than 110º.
  • Subjects who, in the opinion of the Investigator, are able to understand this investigation, co-operate with the investigational procedures and are willing to return to the hospital for all the required post-operative follow-ups.
  • Subjects who present with idiopathic osteoarthritis that in the opinion of the clinical investigator requires a primary total knee arthroplasty.
  • Subjects who in the opinion of the Clinical Investigator are considered to be suitable for treatment with the P.F.C.® Sigma RPF knee, according to the indications specified in the package insert leaflet.
Exclusion Criteria
  • Subjects who, in the opinion of the Investigator, have an existing condition that would compromise their participation and follow-up in this study.
  • Women who are pregnant.
  • Subjects who are known drug or alcohol abusers or with psychological disorders that could effect follow-up care or treatment outcomes.
  • Subjects who have participated in a clinical study with an investigational product in the last month (30 days).
  • Subjects who are currently involved in any personal injury litigation claims.
  • Subjects with a known history of poor compliance to medical treatment.
  • Subjects who have a pre-operative limb deformity of equal to or greater than 10° varus or 15° valgus as defined using the anatomical axis.
  • Subjects who have morbid obesity i.e. BMI ≥40.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
P.F.C. Sigma RP-F Total Knee ReplacementP.F.C. Sigma RP-F Total Knee ReplacementAn orthopaedic implant for total knee replacement with a mobile-bearing and a high flexion design
Primary Outcome Measures
NameTimeMethod
Number of patients with a functionally stable knee that can achieve post-operative range of motion of 125° or greater.1 year

Proportion of cases that have a functionally stable knee (Q10 of Oxford Knee Score is 'rarely/never' or 'sometimes, or just at first'), AND can achieve 1-year post-op passive range of motion of 125 degrees or greater.

Secondary Outcome Measures
NameTimeMethod
SF-12 1, 2, 3, 5, 10, 15 and 20 years1, 2, 3 and 5 years
Survivorship of the P.F.C.® Sigma RPF knee at 1, 2, 3, 5, 10, 15 and 20 years.1, 2, 3 and 5 years
Oxford Knee Score at 1, 2, 3, 5, 10, 15 and 20 years1, 2, 3 and 5 years
Radiographic assessments at 1, 2, 3, 5, 10, 15 and 20 years1, 2, 3 and 5 years
Patellar Score at 1, 2, 3, 5, 10, 15 and 20 years1, 2, 3 and 5 years
American Knee Society Change from Baseline Knee and Function Scores at 1, 2, 3, 5, 10, 15 and 20 years1, 2, 3 and 5 years

Trial Locations

Locations (8)

Kobe University Graduate School Of Medicine, 7-5-1 Kusundki- cho

🇯🇵

Chuoku, Kobe, Japan

Kyunghee University Hospital, 1 HoegiDong

🇰🇷

Dongdaemun Gu, Seoul, Korea, Republic of

The Nook, 51/B SV Road

🇮🇳

Mumbai, Maharashtra, India

Wellington School Of Medicine Surgical Research Trust, Main Street

🇳🇿

Newtown, Wellington, New Zealand

Tan Tock Seng Hospital, No 11 Jalan

🇸🇬

Tan Tock Seng, Singapore

Clifton Park NHS Treatment Centre, Blue Beck Drive, Shipton Road

🇬🇧

York, United Kingdom

Nottingham City Hospital, Hucknell Road

🇬🇧

Nottingham, United Kingdom

Sirriraj Hospital, Mahidol University

🇹🇭

Bangkok, Thailand

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