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OpenTrials
Completed

NCT Number: NCT00319280

Proximal Tibial Open Wedge Osteotomy. A Clinical Prospective, Randomized RSA-trial.

In the treatment of osteoarthritis of the medial compartment of the knee, Open wedge high tibial osteotomy is a good choice of treatment for the young and active patient.

However it leaves an open gap which has to be filled with a bone substitute and requires stable fixation.

Hitherto the golden standard has been autograft taken from iliac crest but there are donorsite related problems and limited amount available.

Recently injectable and resorbable calciumphosphate-cements have been introduced and used with promising results in fractures of the distal radius, calcaneus and lateral tibial condyle.

These new cements seem to be a good alternative to other bone substitutes providing high initial strength that might promote early mobilisation; it resorbs and promotes osteoconduction securing safe healing.

The aim of the present study is to evaluate whether there is any difference in clinical outcome, correction, stability and healing in open-wedge osteotomies with three different bone substitutes: Autograft from iliac crest and the injectable calciumphosphate-cement Calcibon and as control a group with an empty gap.

Osteosynthesis is performed with the Dynafix® system (EBI) The investigation is performed as a randomised prospective clinical trial including 45 patients with a planned 2 years follow-up period.

Clinical outcome is evaluated with: Hospital of special surgery score, KOOS, SF 12 and Lysholm score.

Routine standing x-rays is performed. Stability is assessed with Roentgen Stereophotogrammetric Analysis (RSA) that provides the opportunity of exact 3-dimensional measuring of eventual loss of correction.

This combined with urine and serum bone-healing markers gives a very precise picture of the healing in the bone-gap.

To asses the cartilage of the knee MRI is performed and biochemical markers fore Collagen type II degradation are measured.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 4

Primary location

Northern Orthopaedic Division, Klinik Farsoe, Aalborg University Hospital

Farsø, Northern Jutland, Denmark

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Osteoarthritis of medial compartment of the knee, Ahlbäck gr. 1-2
  • Candidate for proximal tibial medial open-wedge osteotomy
  • Signed informed consent

Exclusion criteria

  • Prednisolone treatment.
  • NSAID treatment.
  • BMI > or = 35.
  • Previous surgery in lateral knee compartment.
  • Secondary Arthrosis following fracture(s) of the tibial condyle(s).
  • Lack of informed consent.

Treatment and study plan

bonesubstitution (Calcibon, Iliac Crest Bonegraft, control)

Procedure

Osteotomysite are filled with Calcibon (an injectable calcium phosphate cement) or Minced Iliac Crest Bonegraft og local graft as control

Primary outcomes

  1. Migration in mm measured with RSA (Roentgen Stereometric Analysis)

    Time frame: postoperative, at 3 month, 1 and 2 years

Secondary outcomes

  1. Hip-Knee-Ankle axis

    Time frame: 3 month, 1 and 2 years.

  2. MR of the knee

    Time frame: 4 weeks preoperative, preoperative, at 1 and 2 years postoperative.

  3. Markers of chondral degradation

    Time frame: preoperative, at 6 weeks, 3 month, 1 and 2 years postoperative

  4. Markers of bone synthesis and degradation

    Time frame: preoperative, at 6 weeks, 3 month, 1 and 2 years postoperative

  5. Clinical scores: KOOS, Lysholm, SF12, Knee Score

    Time frame: Preoperatively, Postoperatively, 6 weeks, 3 months, 1 year and 2 years

  6. Histomorphometric evaluation of bone healing and osseous integration of cement

    Time frame: 1 year

Sponsors and collaborators

Lead sponsor

Northern Orthopaedic Division, Denmark

Other

Collaborators

  • Company CCBR A/S

Registry information

Official study title

Proximal Tibial Open Wedge Osteotomy. Stability and Healing Evaluated in a Clinical Prospective, Randomized Trial Using RSA.

Important dates

Study start
2004
Primary completion
2006
Study completion
2008
First posted
Apr 27, 2006
Registry last updated
Mar 31, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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