Intestinal Microbiota and Vitamin K Levels in PXE Patients (IMPROVE Study)
NCT ID: NCT03813550
Last Updated: 2019-02-04
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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UNKNOWN
NA
20 participants
INTERVENTIONAL
2019-01-21
2020-01-30
Brief Summary
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Detailed Description
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This study will be performed as Research surrounding bio collection "Clinical and biological exploration of PXE patients" kept at the Center of Biological Resources of Angers University Hospital (bio collection n° DC 20116-14-67, authorization to transfer n° 2016-27-99). Fecal samples, plasma samples and clinical data will be collected from patients diagnosed with PXE who will be monitored at the Angers University Hospital Referral Center (France) in 2019-2020. Clinical severity of PXE will be assessed using modified Phenodex score. Gut microbiota will be analyzed using metagenomic sequencing. Plasma Vitamin K species and fecal excretion of menaquinones will be assessed using HPLC. Plasma dp-ucMGP (circulating biomarker of vitamin K status) and serum PIVKA-II (protein induced by vitamin K absence-II) will be assessed using immunoassay. Results will be compared to healthy age- and gender-matched controls from the pre-existing Biofortis database.
Conditions
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Study Design
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NA
SINGLE_GROUP
BASIC_SCIENCE
NONE
Study Groups
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PXE cohort 2019-2020
PXE patient cohort monitored at referral centre from 2019 to 2020: fecal and blood samples
Fecal and blood samples
Fecal samples for intestinal microbiota analysis; Blood and fecal samples for assessment of various forms of vitamin K
Interventions
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Fecal and blood samples
Fecal samples for intestinal microbiota analysis; Blood and fecal samples for assessment of various forms of vitamin K
Eligibility Criteria
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Inclusion Criteria
* Aged over 18 years
* Written consent obtained for Angers University Hospital (France) PXE bio-collection
Exclusion Criteria
* Patients unwilling to participate in the study, or unable to sign the bio-collection consent form
18 Years
ALL
No
Sponsors
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Maastricht University
OTHER
Biofortis Mérieux NutriSciences
OTHER
University Hospital, Angers
OTHER_GOV
Responsible Party
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Principal Investigators
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Ludovic MARTIN, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
Department of Dermatology, University Hospital of Angers
Locations
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Biofortis Mérieux NutriSciences
Saint-Herblain, Pays de la Loire Region, France
Department of Dermatology, University Hospital of Angers
Angers, Pays de Loire, France
Department of Biochemistry, University Maastricht
Maastricht, , Netherlands
Countries
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Central Contacts
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Facility Contacts
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References
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Other Identifiers
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2018/79
Identifier Type: -
Identifier Source: org_study_id
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