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NCT Number: NCT00841152

Comparison of Bioactive Glass and Beta-Tricalcium Phosphate as Bone Graft Substitute

This study is designed to perform a head-to-head comparison of two synthetic ceramic bone graft substitutes, bioactive glass (BAG) and beta-tricalcium phosphate (TCP), in filling of contained bone defects following surgical evacuation of benign bone tumor or tumor-like conditions. Based on the investigators' previous preclinical research and an ongoing single-center randomized clinical trial on bioactive glass filling, the investigators expect BAG filling to be more efficient compared to TCP in promotion of defect healing and functional recovery after surgery.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Helsinki University Hospital, Helsinki, Finland

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About this study

This study is designed to perform a head-to-head comparison of two synthetic ceramic bone graft substitutes, bioactive glass (BAG) and beta-tricalcium phosphate (TCP), in filling of contained bone defects following surgical evacuation of benign bone tumor or tumor-like conditions. Small metacarpal and phalangeal enchondromas (Stratum I) and large long-bone lesions (Stratum II) will be evaluated separately. Aside with the head-to-head comparison of the two synthetic bone graft substitutes, autologous bone graft (Stratum I) and allogeneic bone graft (Stratum II) will be used as the standard of care controls.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Patients with primary or recurrent benign bone tumor or tumor-like condition that requires operative treatment by means of tumor evacuation and defect filling
  • Pathological fractures of patients in Stratum I are treated by means of conservative treatment for three months before tumor surgery

Exclusion criteria

  • History of acute or chronic local infection
  • History of malignancy (excluding carcinoma basocellular) within past 5 years
  • A history of local radiotherapy
  • A known metabolic skeletal disease (such as osteoporosis, Paget's disease or osteomalacia)
  • Medication affecting bone turnover (oral bisphosphonates, PTH, sodium fluoride, strontium ranelate, calcitonin, testosterone, systemic cortico- or anabolic steroids)
  • Any plans to use phenol or other chemical/thermal method of local tumor control
  • Pregnancy
  • Any other condition that in the judgment of the investigator, would prohibit the subject from participating in the study or may hinder the collection of data and interpretation of the results

Treatment and study plan

Bioactive Glass

Device

Surgical implantation

Other names: Bonalive (Vivoxid Ltd, Turku, Finland)

Beta-tricalcium phosphate (ChronOs)

Device

Surgical implantation

Other names: ChronOs (Synthes, Solothurn, Switzerland)

Autograft

Procedure

Surgical transplantation from iliac crest

Allograft (frozen femoral head)

Procedure

Surgical transplantation

Primary outcomes

  1. Stratum I: Hand-grip strength test

    Time frame: 3 months

    Hand and finger grip strength measured by a standard device

  2. Stratum II: Healing of cortical bone window based on CT scan evaluation

    Time frame: 6 months

    CT-evaluation of cortical defect healing

Secondary outcomes

  1. Biomaterial incorporation assessed with radiographs

    Time frame: 3, 6, and 12 months

    Radiographic evaluation of bioactive glass and bone graft incorporation

  2. Pain intensity (VAS)

    Time frame: 3,6, and 12 months

    Evaluation of postoperative pain

  3. Stratum I: DASH-questionnaire

    Time frame: 3,6, and 12 months

    Evaluation of patient-related outcome

  4. RAND-36

    Time frame: 3,6, and 12 months

    Evaluation of patient-related outcome

  5. Surgical wound healing

    Time frame: 0-3 months

    Clinical evaluation of surgical wound healing

  6. Soft tissue complications

    Time frame: 0-12 months

    Clinical evaluation of soft tissue complications in the surgical area

  7. Bone complications

    Time frame: 0-12 months

    Clinical and radiographic evaluation of complications of bone defect healing

Sponsors and collaborators

Lead sponsor

Turku University Hospital

Other Gov

Registry information

Official study title

A National, Prospective, Randomized, Multicenter, Controlled Head-to-Head Comparison of Bioactive Glass and Beta-Tricalcium Phosphate as Bone Graft Substitute in Filling of Contained Bone Defects

Acronym: BAGvsTCP

Important dates

Study start
2009
Primary completion
2014
Study completion
2018
First posted
Feb 11, 2009
Registry last updated
Mar 16, 2021

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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