MedPath

Pinnacle RSA Study

Not Applicable
Terminated
Conditions
Degenerative Arthritis
Osteoarthritis
Interventions
Device: THA
Registration Number
NCT04070989
Lead Sponsor
DePuy Orthopaedics
Brief Summary

The primary objective is to establish the mean superior cup migration of the Pinnacle Acetabular Shell using model-based RSA over the first two years post-implantation. The primary endpoint is the mean vertical subsidence (Y translation, also known as superior cup migration) at 2 years as measured with RSA. This will be summarized for each surgical approach separately, as well as combined.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
84
Inclusion Criteria
  1. Individuals requiring primary THA for a severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia, AVN of the femoral head or acute traumatic fracture of the femoral head or neck
  2. Individuals who are able to speak, read and comprehend the informed patient consent document and willing and able to provide informed patient consent for participation in the study and have authorized the transfer of his/her information to DePuy Synthes
  3. Individuals who are willing and able to return for follow-up as specified by the study protocol
  4. Individuals who are a minimum age of 21 years at the time of consent
  5. Individuals who are willing and able to complete the Subject Hip Outcomes questionnaires as specified by the study protocol
Exclusion Criteria
  1. Individuals have active local or systemic infection
  2. Individuals who have loss of musculature, neuromuscular compromise or vascular compromise that would impact rehabilitation following surgery
  3. Individuals with poor bone quality, such as osteoporosis, where in the surgeon's opinion, there could be considerable migration of the prosthesis or require additional acetabular cup fixation using screws, or a significant chance of fracture of the femoral shaft and/or the lack of adequate bone to support the implant(s)
  4. Individuals with Charcot's or Paget's disease
  5. Individuals who, in the judgement of the investigator, would not be a candidate for protocol allowable components to be used for their THA
  6. Women that are pregnant or lactating
  7. Individuals who have had a contralateral hip that was implanted less than 6 months prior to the time of consent into this study or individuals that expect to have a contralateral hip implanted in the following 6 months at the time of consent into this study
  8. Individuals that have amputations in either leg that would impact rehabilitation following surgery
  9. Individuals who are bedridden.
  10. Individuals that have participated in a clinical investigation with an investigational product (drug or device) in the last three months
  11. Individuals currently involved in any personal injury litigation, medical-legal or worker's compensation claims
  12. Individuals, in the opinion of the Investigator, who are drug or alcohol abusers or have psychological disorders that could affect their ability to complete patient reported questionnaires or be compliant with follow-up requirements
  13. Individuals diagnosed and taking prescription medications to treat a muscular disorder that limits mobility due to severe stiffness and pain such as fibromyalgia or polymyalgia
  14. Subject has a medical condition with less than 2 years life expectancy
  15. Individual has a BMI >45 kg/m2.

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
Posterior ApproachTHAPinnacle Acetabular Shell (Sector, Gription, no screws), AltrX Polyethylene Liner and Corail Femoral Stem implanted via the posterior approach
Lateral ApproachTHAPinnacle Acetabular Shell (Sector, Gription, no screws), AltrX Polyethylene Liner and Corail Femoral Stem implanted via the lateral approach
Anterior ApproachTHAPinnacle Acetabular Shell (Sector, Gription, no screws), AltrX Polyethylene Liner and Corail Femoral Stem implanted via the anterior approach
Primary Outcome Measures
NameTimeMethod
Mean superior cup migration (subsidence) at 2 years2 years

RSA measured mean superior cup migration (subsidence: Y translation in mm) at 2 years for each surgical approach separately, as well as combined

Secondary Outcome Measures
NameTimeMethod
Z-axis rotation of the acetabular shell at 1 year1 year

RSA measured Z-axis rotation of the acetabular shell measured in degrees

X-axis translation of acetabular shell at 3 months3 months

RSA measured X-axis translation of acetabular shell in mm

Maximal total point motion of the acetabular shell at 3 months3 months

RSA measured maximal total point motion of the acetabular shell in mm

X-axis translation of acetabular shell at 6 months6 months

RSA measured X-axis translation of acetabular shell in mm

Z-axis translation of acetabular shell at 6 months6 months

RSA measured Z-axis translation of acetabular shell in mm

FJS-12 at 3 months3 months

Functional and health status as measured with the Forgotten Joint Score (FJS-12). This is a validated score that assesses patient outcomes. The result range is 0-100 where a higher score mean a more favorable result.

RSA measured cup subsidence at 6 months6 months

RSA measured subsidence (in mm) of the Pinnacle Acetabular Shell

Z-axis rotation of the acetabular shell at 6 months6 months

RSA measured Z-axis rotation of the acetabular shell measured in degrees

Harris Hip Score at 3 months3 months

Functional and health status as measured with the Harris Hip Score. This is a validated scoring system of the hip that has a result range of 0-100; the higher the score, the better the patient outcome.

X-axis rotation of the acetabular shell at 3 months3 months

RSA measured X-axis rotation of the acetabular shell measured in degrees

RSA measured cup subsidence at 3 months3 months

RSA measured subsidence (in mm) of the Pinnacle Acetabular Shell

Z-axis translation of acetabular shell at 3 months3 months

RSA measured Z-axis translation of acetabular shell in mm

HOOS Jr. Score at 3 months3 months

Functional and health status as measured with the HOOS Jr. score. This is a short version of the HOOS (hip disability and osteoarthritis outcome score) that has a result range of 0-100. A score of 0 indicates total hip disability and 100 indicates perfect hip health.

X-axis translation of acetabular shell at 1 year1 year

RSA measured X-axis translation of acetabular shell in mm

Z-axis translation of acetabular shell at 1 year1 year

RSA measured Z-axis translation of acetabular shell in mm

X-axis translation of acetabular shell at 2 years2 years

RSA measured X-axis translation of acetabular shell in mm

Linear head penetration at 2 years2 years

Amount of linear head penetration compared to baseline (6 weeks) measured in mm

Y-axis rotation of the acetabular shell at 3 months3 months

RSA measured Y-axis rotation of the acetabular shell measured in degrees

Y-axis rotation of the acetabular shell at 6 months6 months

RSA measured Y-axis rotation of the acetabular shell measured in degrees

Y-axis rotation of the acetabular shell at 1 year1 year

RSA measured Y-axis rotation of the acetabular shell measured in degrees

Z-axis rotation of the acetabular shell at 3 months3 months

RSA measured Z-axis rotation of the acetabular shell measured in degrees

Maximal total point motion of the acetabular shell at 6 months6 months

RSA measured maximal total point motion of the acetabular shell in mm

Harris Hip Score at 6 months6 months

Functional and health status as measured with the Harris Hip Score. This is a validated scoring system of the hip that has a result range of 0-100; the higher the score, the better the patient outcome.

HOOS Jr. Score at 6 months6 months

Functional and health status as measured with the HOOS Jr. score. This is a short version of the HOOS (hip disability and osteoarthritis outcome score) that has a result range of 0-100. A score of 0 indicates total hip disability and 100 indicates perfect hip health.

RSA measured cup subsidence at 1 year1 year

RSA measured subsidence (in mm) of the Pinnacle Acetabular Shell

Maximal total point motion of the acetabular shell at 1 year1 year

RSA measured maximal total point motion of the acetabular shell in mm

Harris Hip Score at 1 year1 year

Functional and health status as measured with the Harris Hip Score. This is a validated scoring system of the hip that has a result range of 0-100; the higher the score, the better the patient outcome.

HOOS Jr. Score at 1 year1 year

Functional and health status as measured with the HOOS Jr. score. This is a short version of the HOOS (hip disability and osteoarthritis outcome score) that has a result range of 0-100. A score of 0 indicates total hip disability and 100 indicates perfect hip health.

FJS-12 at 1 year1 year

Functional and health status as measured with the Forgotten Joint Score (FJS-12). This is a validated score that assesses patient outcomes. The result range is 0-100 where a higher score mean a more favorable result.

X-axis rotation of the acetabular shell at 6 months6 months

RSA measured X-axis rotation of the acetabular shell measured in degrees

X-axis rotation of the acetabular shell at 1 year1 year

RSA measured X-axis rotation of the acetabular shell measured in degrees

Z-axis translation of acetabular shell at 2 years2 years

RSA measured Z-axis translation of acetabular shell in mm

Z-axis rotation of the acetabular shell at 2 years2 years

RSA measured Z-axis rotation of the acetabular shell measured in degrees

HOOS Jr. Score at 2 years2 years

Functional and health status as measured with the HOOS Jr. score. This is a short version of the HOOS (hip disability and osteoarthritis outcome score) that has a result range of 0-100. A score of 0 indicates total hip disability and 100 indicates perfect hip health.

FJS-12 at 6 months6 months

Functional and health status as measured with the Forgotten Joint Score (FJS-12). This is a validated score that assesses patient outcomes. The result range is 0-100 where a higher score mean a more favorable result.

Maximal total point motion of the acetabular shell at 2 years2 years

RSA measured maximal total point motion of the acetabular shell in mm

X-axis rotation of the acetabular shell at 2 years2 years

RSA measured X-axis rotation of the acetabular shell measured in degrees

Harris Hip Score at 2 years2 years

Functional and health status as measured with the Harris Hip Score. This is a validated scoring system of the hip that has a result range of 0-100; the higher the score, the better the patient outcome.

Linear head penetration at 1 year1 year

Amount of linear head penetration compared to baseline (6 weeks) measured in mm

Y-axis rotation of the acetabular shell at 2 years2 years

RSA measured Y-axis rotation of the acetabular shell measured in degrees

FJS-12 at 2 years2 years

Functional and health status as measured with the Forgotten Joint Score (FJS-12). This is a validated score that assesses patient outcomes. The result range is 0-100 where a higher score mean a more favorable result.

Trial Locations

Locations (3)

London Health Sciences Centre

🇨🇦

London, Ontario, Canada

QEII Health Sciences Centre & Dalhousie University

🇨🇦

Halifax, Nova Scotia, Canada

Concordia Joint Replacement Group, Concordia Hip and Knee Institute & University of Manitoba

🇨🇦

Winnipeg, Manitoba, Canada

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