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Patient-specific Instruments as a Standard Procedure in Total Knee Arthroplasty

O

Orthopedic Clinic Gersthof

Status

Completed

Conditions

Alignment

Treatments

Device: Total knee arthroplasty (TKA) (Smith &Nephew®)

Study type

Observational

Funder types

Other

Identifiers

Details and patient eligibility

About

Description of logistics, learning curve and radiological results in 70 patients treated with patient specific instrumentation in total knee arthroplasty as a standard procedure

Full description

The Orthopaedic Clinic Gersthof is a teaching hospital, where the entire spectrum of joint replacements with emphasis on hips and knees is performed. Twenty surgeons perform TKAs at our institution, with approximately 400 TKAs implanted per year.

The PSI system of Smith &Nephew® (Patient-Matched Cutting Blocks [PMCB]; the VISIONAIRE® technology) is applied. The preoperative image modality is based on a long leg standing X-ray as well as an MRI of the knee. The Genesis II® Endoprosthesis (Smith & Nephew®) is used as the TKA implant.

This study is a observational monocentric prospective study.

Estimated enrollment: 70 Enrollment time: September 2011-October 2012 Primary outcome: Alignment

The postoperative X-rays (AP, lateral view, and long leg standing), taken 7-to-10 days after surgery are evaluated in terms of component position and restoration of the mechanical alignment. X-rays are routinely monitor-guided but not calibrated at our institution.

As a secondary outcome the learning curve is evaluated using the following parameters collected during surgery: the fit of the cutting blocks, changes of the implant size, bony recuts, soft tissue releases, and changes in inlay size. Gap balancing was subjectively judged by the operating surgeon. Operation time, number of blood transfusions, and early postoperative complications were recorded within the first 14 days after surgery.

Enrollment

73 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Indication for TKA
  • Genesis II endoprosthesis
  • Operated using patient specific instruments (VISIONAIRE)

Exclusion criteria

  • contraindication for MRI
  • varus/ valgus deformity >15 degrees

Trial design

73 participants in 1 patient group

Patients treated with Patient specific instruments in TKA
Treatment:
Device: Total knee arthroplasty (TKA) (Smith &Nephew®)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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