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Characteristics and Outcomes of Odontoid Fragility Fractures in Elderly

Characteristics and Outcomes of Odontoid Fragility Fractures in Elderly

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02800278
Acronym
FOOP
Enrollment
30
Registered
2016-06-15
Start date
2016-01-01
Completion date
2018-12-31
Last updated
2026-06-16

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

Conditions

Odontoid Fracture, Osteoporosis, Surgery

Brief summary

Usually, cervical spine fractures are not considered as osteoporotic fractures. However, recent studies show that odontoid fractures are the most common fractures of the cervical spine in elderly and may occur in a context of low trauma energy. Thus, the goal of this observationnal study is : * to describe the different type of odontoid fracture and to characterize bone status in elderly patient (\>65 y) who underwent odontoid fracture in a context of low trauma energy. * To describe short and long term outcomes

Detailed description

All patients over 65 y admitted for low trauma odontoid fracture will be consecutively included in the study after informed consent. The investigators will record: * clinical risk factor of osteoporosis and health habits including accomodation * type of fracture and characterization of the odontoid fracture on imaging (standard X ray / MRI / QCT) * Bone status : bone mineral density on DXA, lab tests for secondary osteoporosis check-up, previous vertebral fracture on VFA or X ray * osteoporosis managment : nutrition, vitamin D, anti-osteoporotic drugs * treatment of the fracture : surgical / non surgical * adverse event during hospitalization * lenght of hospital stay * type of discharge Follow-up à 3 and 12 months : dead vs alive ; accomodation ; autonomy ; new fracture

Interventions

OTHERobservational

describe bone status and outcome of odontoid fracture

Sponsors

Centre Hospitalier Universitaire de Nice
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

* all patients over 65 y admitted for low traumat odontoid fracture

Exclusion criteria

* patient \< 65 y * traumatic odontoid fracture

Design outcomes

Primary

MeasureTime frameDescription
bone status at the time of odontoid fracture: bone mineral density, prevalent osteoporotic fracture, vitamin D statusfrom date of inclusion until to 3 weeks after the event. Inclusion will be proposed within 2 weeks after the fractureclinical risk factor of osteoporosis, prevalent clinical osteoporotic fracture, bone mineral density measured by DXA, vertebral fracture assessment to detect other vertebral fracture, serum concentration in 25OHvitamin D

Secondary

MeasureTime frameDescription
mortalityduring hospitalization - 3 and 12 months after inclusionmortality after odontoid fracture during hospitalization and at 3 and 12 monts
morbidityduring hospitalization - 3 and 12 months after inclusionincident osteoporotic fracture, adverse event such as infection, cardiovascular event, neurological event
loss of autonomydischarge, 3 and 12 monthslenght of hospital stay, type of discharge (home, nursing home, rehabilitation bed care, institutionalized accomodation

Countries

France

Contacts

PRINCIPAL_INVESTIGATORveronique breuil, MD, PhD

Centre Hospitalier Universitaire de Nice

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Jun 17, 2026