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Effectiveness of Medical Management of Fibrous Dysplasia of Bone.

Completed
Conditions
Fibrous Dysplasia of Bone
McCune Albright Syndrome
Registration Number
NCT05422833
Lead Sponsor
Hospices Civils de Lyon
Brief Summary

The objective of our study was to assess the effectiveness of our reference center since its constitution.

In a retrospective cohort study, we compared the activity of our center, including the time elapsed between diagnosis and access to the center and the diagnostic delay of patients with fibrous dysplasia between two periods, 1996-2006 (before certification of our center) and 2007-2019 (after certification of our center).

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
528
Inclusion Criteria

We have included children and adults with FD/MAS who visited at least once in our center (outpatient and hospitalized patients). The diagnosis was established by an expert of the center, based on clinical, biological, imaging and/or histological arguments

Exclusion Criteria

The absence of detectable bone lesion

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
to compare time elapsed between first symptomes or discovery of bone lesions and the diagnosis of FD1996-2019

The main objective was to compare time elapsed between first symptomes or discovery of bone lesions and the diagnosis of FD, over 2 periods of time: 1996-2006 (before certification) and 2007-2019 (after certification).

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

rheumatology department, hopital Edouard Herriot

🇫🇷

Lyon, France

rheumatology department, hopital Edouard Herriot
🇫🇷Lyon, France

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