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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06177327
Other study ID # 23-5288
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 19, 2024
Est. completion date December 12, 2025

Study information

Verified date February 2024
Source Hospices Civils de Lyon
Contact Roland Chapurlat, MD, PhD
Phone + 33 (0)4 72 11 74 82
Email roland.chapurlat@chu-lyon.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Fibrous dysplasia of bone /McCune Albright syndrome (FD/MAS) is a rare bone disease caused by somatic mutations in GNAS gene. This GNAS mutation predisposes to cancers, including breast cancer, thyroid cancer, chondrosarcoma and osteosarcoma, as well as biliary tract anomalies, liver-tumors or pancreatic tumors - IPMNs. Intraductal papillary and mucinous neoplasms of the pancreas (IPMN) are cystic intraepithelial ductal lesions developed at the expense of pancreatic ducts. They are pre-cancerous lesions, requiring monitoring and, in case of progression or malignant degeneration, surgical resection. Pancreatic MRI screening of patients with polyostotic FD and MAS is recommended. The aim of this study is to investigate the epidemiology and characteristics of these hepato-pancreato-biliary abnormalities (prevalence, age of onset, degeneration), based on magnetic resonance imaging (MRI) realized during the follow-up of patients with FD/MAS treated in a French FD expert center. A better understanding of these IPMNs and other digestive abnormalities will enable clinicians to improve the management and monitoring in this high-risk population.


Recruitment information / eligibility

Status Recruiting
Enrollment 545
Est. completion date December 12, 2025
Est. primary completion date November 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria: - Adults =18 years with polyostotic FD/MAS - Followed up in the national FD reference center (Lyon) or in a FD French expert center: Angers, Bordeaux, Brest, Caen, Clermont-Ferrand, Lille, Marseille, Montpellier, Nice, Paris, Poitiers, Rennes, Saint-Etienne, Strasbourg. - who had an hepato-bilio-pancreatic MRI during their follow-up, since January 2002 - No objection to data collection Exclusion Criteria: -Opposition to data collection

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Screening for hepato-bilio-pancreatic abnormalities in Fibrous dysplasia of bone /McCune Albright syndrome , description and characterization of the lesions.
Data collection from hepato-bilio-pancreatic Magnetic Resonance Imaging realized during the follow up of patients with Fibrous dysplasia of bone /McCune Albright syndrome

Locations

Country Name City State
France CHU Angers Angers
France Groupe Hospitalier Pellegrin - Chu Bordeaux
France CHU de Brest - Hôpital de la Cavale Blanche Brest
France Chu de Caen Normandie Caen
France Chu de Clermont-Ferrand Clermont-Ferrand
France Chu de Lille Lille
France Service Rhumatologie, pavillon F Hopital E. Herriot Lyon
France Assistance Publique - Hopitaux de Marseille (Ap-Hm Marseille
France Chu de Montpellier Montpellier
France CHU de Nice Nice
France Assistance Publique - Hopitaux de Paris (Ap-Hp) Paris
France CHU de Poitiers Poitiers
France Chu de Rennes Rennes
France Chu de Saint-Etienne Saint-Étienne
France Hopitaux Universitaires de Strasbourg Strasbourg
France Chu de Toulouse Toulouse

Sponsors (1)

Lead Sponsor Collaborator
Hospices Civils de Lyon

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Describe hepato-bilio-pancreatic abnormalities in FD/MAS and estimate the prevalence of IPMN. Hepato-bilio-pancreatic abnormalities (size, number, complications) will be described based on hepato-bilio-pancreatic MRI. hepato-bilio-pancreatic MRI performed from January 2002 until December 2024.
See also
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Completed NCT05422833 - Effectiveness of Medical Management of Fibrous Dysplasia of Bone.
Recruiting NCT03838991 - Epigenetic Regulation in Fibrous Dysplasia of Bone: mirDYS Study. N/A
Active, not recruiting NCT05509595 - Burosumab for Fibroblast Growth Factor-23 Mediated Hypophosphatemia in Fibrous Dysplasia Phase 2