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Clinical Trials/NCT02316704
NCT02316704
Active, not recruiting
Not Applicable

Fixation of OsseoTi™ Porous Structure Versus PPS (Porous Plasma Spray) Coating on the G7™ Acetabular Component for Primary Total Hip Arthroplasty: A Single-Blinded Randomized Controlled Trial Evaluating Implant Migration, Acetabular Liner Wear, and Patient Reported Outcome

Hvidovre University Hospital2 sites in 2 countries98 target enrollmentDecember 2014
ConditionsOsteoarthritis

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Osteoarthritis
Sponsor
Hvidovre University Hospital
Enrollment
98
Locations
2
Primary Endpoint
RSA migration in 3 dimentions of the acetabular components as measured by Radiostereometric analysis, RSA.
Status
Active, not recruiting
Last Updated
5 years ago

Overview

Brief Summary

The primary objective of this project is to investigate, using RSA, acetabular implant migration of the OsseoTi™ G7 acetabular cup in comparison to conventional PPS coated G7 acetabular cup, and compare liner wear of thinnest available E1™ liner, allowing for the largest possible femoral head (36mm-44mm) to E1™ liner holding a 32mm femoral head in the G7 acetabular system with endpoint assessment being performed at the 2 year follow-up.

Registry
clinicaltrials.gov
Start Date
December 2014
End Date
April 2027
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Kirill Gromov

MD, PhD

Hvidovre University Hospital

Eligibility Criteria

Inclusion Criteria

  • • Participants with primary hip osteoarthritis set to receive a primary unilateral uncemented total hip arthroplasty.
  • Participants must be 18-75 years of age.
  • Participants must be able to speak and understand Danish (or depending on country where patient is enrolled).
  • Participants must be able to give informed consent and be cognitively intact.
  • Participants must be expected to be able to complete all postoperative controls.
  • Participants must not have severe comorbidities, ASA-score ≤ 3.

Exclusion Criteria

  • Terminal illness.
  • Rheumatoid arthritis.
  • Previous fracture of the hip.
  • Osteonecrosis of the hip.
  • Previous infection of the hip.
  • Severe bony deformity warranting the use of non-standard implants.
  • Metastasis in the periarticular bone or proximal femur.
  • Female patients that are pregnant or planning pregnancy during follow-up period
  • If bone stock or femoral canal type, assessed on preoperative x-ray, warrants the use of cemented fixation.
  • Documented osteoporosis with patient in active medical treatment.

Outcomes

Primary Outcomes

RSA migration in 3 dimentions of the acetabular components as measured by Radiostereometric analysis, RSA.

Time Frame: 2 year

Radiostereometric analysis, RSA, is an accurate technique for measuring small relative motions from sequential sets of radiographs over time and has been used to measure polyethylene wear and implant migration. Measurements are performed in microns.

Study Sites (2)

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