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Osteonecrosis of the Jaw (ONJ) Case Registry

Osteonecrosis of the Jaw (ONJ) Case Registry

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01666106
Enrollment
327
Registered
2012-08-16
Start date
2012-10-01
Completion date
2020-12-16
Last updated
2020-12-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Osteonecrosis of the Jaw

Brief summary

Osteonecrosis of the Jaw (ONJ) Case Registry

Detailed description

The purpose of the ONJ case registry is to describe the natural history of positively-adjudicated ONJ in subjects with cancer with an observation period of 5 years. Most of these subjects are expected to have received bone antiresorptive agents such as bisphosphonates or denosumab together with cancer-specific therapies (eg, chemotherapy, steroids, or anti-angiogenics). It is also possible that the registry will include subjects with cancer who developed ONJ without exposure to any antiresorptive therapy.

Interventions

None listed

Sponsors

Amgen
Lead SponsorINDUSTRY

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adult (≥18 years of age) with diagnosis of cancer * Newly diagnosed, positively-adjudicated ONJ * ECOG \<=2 and expected survival ≥3 months * Willing to provide access to previous and future medical and dental information * Subject or subject's legally acceptable representative has provided written informed consent

Exclusion criteria

* History of radiation to the jaws administered for the treatment of cancer * Subject will not be available for protocol required study visits, to the best of the subject and investigator's knowledge. * Subject has any kind of disorder that, in the opinion of the investigator, may compromise the ability of the subject to give written informed consent and/or to comply with all required study procedures.

Design outcomes

Primary

MeasureTime frameDescription
Resolution rate and time to ONJ resolution5 years* Resolution: complete coverage of the exposed bone by mucosa in the absence of clinical symptoms * Improvement: a decrease in the stage or severity of the lesion * Progression: an increase in the stage or severity of the lesion * Stable: not resolved, improved, or progressed

Secondary

MeasureTime frameDescription
The clinical features of ONJ, including severity and staging at enrollment5 years
The frequency of risk factors for incident ONJ5 yearsCharacterize the frequency of risk factors for incident ONJ such as a history of inflammatory dental disease (periodontal and dental abscesses), dentoalveolar procedures, smoking, use of antiangiogenic agents, and duration/dosing regimens of antiresorptive medications prior to the development of ONJ
Therapeutic treatment patterns for ONJ5 yearsCharacterize treatment patterns of antiresorptive medications subsequent to incident ONJ such as the proportion of subjects who continue to be treated with antiresorptive medications by specific agents and ONJ severity and stage
Treatment patterns of antiresorptive agents subsequent to incident ONJ5 yearsCharacterize subsequent treatment patterns for ONJ including antimicrobial oral rinses, antibiotics, and surgery

Countries

Belgium, Canada, Denmark, Finland, France, Germany, Greece, Italy, Spain, United Kingdom, United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026