Treatment Trials

5 Clinical Trials for Various Conditions

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      TERMINATED
      Feasibility Study of Aastrom Tissue Repair Cells to Treat Non-Union Fractures.
      Description

      The purpose of this multi-center study is to obtain clinical data to substantiate that Aastrom TRC autologous bone marrow cells will regenerate bone in patients with established (appendicular skeletal) non union fractures, when used with one of the commonly employed commercially available allograft chip matrices.

      Conditions
      Fracture, UnunitedPseudarthrosis
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      RECRUITING
      Safety, Efficacy, & Use of ViviGen Cellular Bone Matrix Allograft in Orthopaedic Fracture Care
      Description

      Prospective registry and retrospective data collection study to assess the efficacy and safety of Vivigen Cellular Bone Matrix (Vivigen) in orthopaedic trauma patients who require bone grafting in the acute, delayed, non-union fracture as well as use in fusion procedure settings.

      Conditions
      Fractures, BoneNonunion of FractureFractures, OpenFractures, UnunitedFracture, TibialFracture of FemurFracture Arm
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      TERMINATED
      A Clinical Registry to Collect Patient Outcome Date for the BIOMET® Stimulator Systems
      Description

      The purpose of this clinical registry is to capture data on an ongoing basis from a population of patients who will use Biomet's BHS, OrthoPak and SpinalPak devices.

      Conditions
      Fusion of Spine (Disease)Fractures, Ununited
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      TERMINATED
      Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder Arthroplasty
      Description

      The objectives of this study are to obtain survival and outcome data on the Trabecular Metal Humeral Stem when used in primary, total or hemi shoulder arthroplasty.

      Conditions
      OsteoarthritisRheumatoid ArthritisPost-traumatic ArthritisUnunited Humeral Head FractureIrreducible 3- and 4-part Proximal Humeral FracturesAvascular Necrosis
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      ACTIVE_NOT_RECRUITING
      Outcomes Study of the Trabecular Metal (TM) Reverse Shoulder System
      Description

      The objectives of this study are to obtain survival and outcome data on the Trabecular Metal Reverse Shoulder System when used in primary or revision reverse total shoulder arthroplasty.

      Conditions
      OsteoarthritisRheumatoid ArthritisPost-traumatic ArthritisUnunited Humeral Head FractureIrreducible 3-and 4-part Proximal Humeral FracturesAvascular NecrosisGross Rotator Cuff DeficiencyRevision Total Shoulder Arthroplasty
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