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Interest of Serum Periostin Dosage in Patients With Bone Fibrous Dysplasia

Interest of Serum Periostin Dosage in Patients With Bone Fibrous Dysplasia

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02868645
Acronym
PERIOSTINE
Enrollment
65
Registered
2016-08-16
Start date
2016-05-25
Completion date
2018-04-10
Last updated
2025-12-19

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

Conditions

Bone Fibrous Dysplasia

Brief summary

Fibrous dysplasia is a rare bone disease which can cause pain and fractures. It has been shown that periostin is over expressed in fibrous component in patients bones ; but periostin has never been measured out in serum of patients, although it is easy to assess. This study aims to show whether serum periostin is elevated in serum of patients with fibrous dysplasia, and if it is more elevated in patients with severe forms of the disease.

Interventions

BIOLOGICALBlood sampling

Patients with bone fibrous dysplasia will have blood sampling to assess periostin rate in serum

Sponsors

Hospices Civils de Lyon
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

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

Inclusion criteria

* patients with fibrous dysplasia of the bone * access to social security * informed consent

Exclusion criteria

* no informed consent * pregnancy * patients with a history of conditions known to increase periostin serum (stade IV cancer, severe asthma, pulmonary fibrosis…)

Design outcomes

Primary

MeasureTime frame
Periostin rate in serumAt inclusion

Secondary

MeasureTime frame
Periostin rate in serum according to the number of fibrotic bonesAt inclusion
Periostin rate in serum in patients with severe phenotype of the diseaseAt inclusion
Periostin rate in serum in patients with Mac Cune Albright syndromeAt inclusion

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026