NCT04217538

Observational Study of a Cohort of Patients With Hereditary Epidermolysis Bullosa

Observational Study of a Cohort of Patients With Hereditary Epidermolysis Bullosa That Come for Their Annual/Biannual Check up at This Medical Rare Disease Reference Centers (MRDRC) of This Disease in France and Belgium

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 41 (actual)
• Sponsor: Centre Hospitalier Universitaire de Nice · Academic / Other
• Sex: All
• Age: 7 Months – 78 Years
• Healthy volunteers: —

Summary

Hereditary Epidermolysis Bullosa (EBH) are rare dermatologic diseases characterized by cutaneous and mucosa fragility. Oral manifestations of few small cohort have been published. The main objective of this multicentric cohort study first in Europe was to report the oral status of these patients that were consulted in the MRDRC of this disease in Nice (France), Toulouse (France) and Louvain (Belgium). Then a correlation between the oral characteristics and the EBH type will be made, in order to facilitate the management of patient care and the prevention program that can be established to improve their oral health.

Conditions

• Epidermolysis Bullosa

Interventions

Type	Name	Description
OTHER	clinical exam	clinical oral examination

Timeline

• Start date: 2017-01-04
• Primary completion: 2019-12-11
• Completion: 2019-12-11
• First posted: 2020-01-03
• Last updated: 2020-01-03

Locations

2 sites across 1 country: France