Condition: Osteoporosis · Sponsor: CHU de Quebec-Universite Laval
Osteoporosis is a multifactorial disease in which genetic predispositions play a key role in its development. A better understanding of family history and clinical manifestations among first- and second-degree relatives can help improve early detection and personalized care for at-risk patients. To this end, we will test a self-administered questionnaire previously developed by our research team. This questionnaire includes the main manifestations associated with rare genetic bone diseases such as osteogenesis imperfecta, hypophosphatasia, and osteopetrosis.
This description comes directly from the study's public registry record.
Laetitia Michou, MD PhD · +14185254444 · laetitia.michou@crchudequebec.ulaval.ca
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| CHU de Quebec-Universite Laval | Québec, Quebec, Canada | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07067827