Phase
Condition
N/ATreatment
ZetaFuse™ Bone Graft
ZetaMet™ (ZetaFuse™ Bone Graft)
Clinical Study ID
Ages 22-75 Female
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Age between 22 (inclusive) and 75 years (inclusive) at the time of enrollment.
Life expectancy of 12 months or more.
Female patient with histologically confirmed diagnosis of primary breast cancer.
Metastatic breast cancer to bone, with or without involvement of other sites (patients with single metastasis qualify)
At least one lytic metastatic lesion located in the vertebral body of the spine.
Normal spinal alignment.
SINS ≥3 and ≤9.
Signed and dated Informed Consent Form (ICF).
Patient is willing and able to participate in required follow-up visits at theInvestigational Site and to complete study procedures and questionnaires.
Exclusion
Exclusion Criteria:
Vertebral body collapse.
Spinal cord compression.
Known allergy to Investigational Device materials.
Using medications or any drug known to potentially interfere with bone/soft tissuehealing (e.g., chronic systemic steroids).
Current tobacco smoker or stopped smoking in past 6 months.
Uncontrolled diabetes mellitus, HbAIC cutoff.
An active systemic infection (e.g., hepatitis, acquired immunodeficiency syndrome (AIDS), AIDS-related complex (ARC).
Currently participating in any investigational trial not related to this trial.
Any other severe acute or chronic medical condition that may interfere with theinterpretation of the trial results, in the judgment of the PI, which would make thepatient inappropriate for entry into this trial.
Pregnant or planning to become pregnant during the trial.
Study Design
Study Description
Connect with a study center
Vancouver Coastal Health Research Institute
Vancouver, British Columbia V5Z 1M9
CanadaSite Not Available
McGill University Health Center
Montréal, Quebec H3G1A4
CanadaSite Not Available
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