Fibromuscular DysplasiaFEIRINCT04804683
European/International FMD Registry and Initiative
A study testing Genetic dissection of Fibromuscular Dysplasia and Search for diagnostic and prognostic biomarkers of Fibromuscular Dysplasia in people with Fibromuscular Dysplasia, run by Cliniques universitaires Saint-Luc- Université Catholique de Louvain at 1 site in Belgium.
Trial summary
The main objectives of FEIRI are: (i) To describe the demographic and arterial characteristics of FMD and related diseases at a global scale and according to countries and/or ethnic origin (ii) To evaluate the incidence and predictors of novel FMD lesions and complications (iii) To explore the commonalities and… Read more about this study
- Who is it for?
- Any age
- Conditions the study is for
- Fibromuscular Dysplasia
- What is being tested?
- Genetic dissection of Fibromuscular Dysplasia and Search for diagnostic and prognostic biomarkers of Fibromuscular Dysplasia
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 5,000 participants
- Where
- 1 siteBelgium
- Study dates
- 11 Mar 2021to 10 Mar 2031
- Phase
- Interventional
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Any age
- All sexes
- No healthy volunteers
- Child, Adult, Older adult
Who may be able to join
- Patients with established FMD, i.e at least one string-of-beads (multifocal FMD) or focal stenosis (focal FMD).
- Patients with Spontaneous Coronary Artery Dissection (SCAD) in whom at least one lesion of multifocal FMD (string-of beads) in extra-coronary arteries has been identified ("SCAD-FMD").
- Patients with so-called "atypical FMD" or "FMD-like presentation", i.e. patients presenting with at least one dissection or 2 aneurysms < 60-year-old, in the absence string-of-beads, focal stenosis or evidence of inherited arteriopathy.
Who cannot join
- Diagnosis based only on ultrasound (need for computed tomographic angiography , magnetic resonance angiography or catheter-based angiography to confirm the diagnosis)
Trial locations and contacts
1 site in 1 country. Contact the study team or a site near you to ask about taking part.
Belgium1 site, 1 recruiting
- Recruiting
Cliniques Universitaires Saint-Luc
Brussels, 1200
Alexandre Persu, MD-PhD, 0032 2 764 63 06, alexandre.persu@uclouvain.be
About this study
Official title: The European/International FMD Registry and Initiative (FEIRI), a Prospective Study
The main objectives of FEIRI are:
(i) To describe the demographic and arterial characteristics of FMD and related diseases at a global scale and according to countries and/or ethnic origin
Read more
(ii) To evaluate the incidence and predictors of novel FMD lesions and complications
(iii) To explore the commonalities and differences between FMD, SCAD and so-called atypical FMD (patients with multiple dissections and/or aneurysms without string-of-beads, focal stenosis or evidence of inherited arteriopathy)
(iv) To contribute to the unravelling of genetic, proteomic and molecular mechanisms underlying FMD and related diseases
Participation to the FEIRI study implies:
(i) Collection of demographic and standard-of-care clinical data, both retrospectively (from the diagnosis of FMD to signature of the informed consent) and prospectively (on the occasion of standard-of-care follow-up).
(ii) Optional participation to a biobank implying collection of blood, urine and, in rare cases of intervention, tissue samples for genomic and proteomic analysis and identification of diagnostic and prognostic biomarkers of FMD.
Participants will be enrolled in centres from over 20 countries in Europe and beyond.
Read the detailed description
Fibromuscular dysplasia (FMD) is an idiopathic, segmental, nonatherosclerotic, and noninflammatory disease of the musculature of arterial walls, leading to stenosis of small- and medium-sized arteries. FMD can be classified in multifocal FMD, characterized by alternation of stenosis and dilations ("string-of-beads") and focal FMD, corresponding to a solitary narrowing. While for long FMD was considered as a rare cause of renovascular disease mostly affecting young women, during the last decades, joint international efforts have led to a thorough reappraisal of the disease. In summary, (i) FMD is no more considered as a truly rare disease; (ii) FMD may be also diagnosed in men (10-20%) and at all ages; (iii) beyond arterial stenosis, FMD is often associated with dissections, aneurysms and arterial tortuosity; (iv) FMD is not restricted to renal arteries and often affects two or more arterial beds; (iv) multifocal FMD lesions are frequent in patients with Spontaneous Coronary Artery Dissection (SCAD).
Despite traditional views on the role of female hormones, mechanical factors and smoking, the pathophysiology of FMD remains largely unknown. In the last decade, research has been focused on genetic dissection of the disease and identification of biomarkers. Recent advances include: (i) identification of an association between FMD and an intronic variant of the Phosphatase and actin regulator 1 (PHACTR1) gene; (ii) identification of rare mutations in several genes such as Prostaglandin I2 Receptor (PTGIR) and Collagen type V alpha 1 chain (COL5A1) genes; (iii) documentation of mild Connective-Tissue Disease-like features and increased levels of Transforming Growth Factor-beta in patients with FMD; (iv) identification of a tentative proteo-genomic signature of the disease. All elements are thus in place to further dissect the pathophysiology of FMD and related diseases, refine clinical characterization, identify predictors of complications and improve screening, management and follow-up.
Unravelling the clinical characteristics, genetic and molecular basis of FMD nevertheless requires large numbers of well characterized patients. In order to address these challenges and generate new evidence pertaining to FMD and associated diseases, we aimed to create an overarching resource and study named "the European/International FMD Registry and Initiative" (acronym: FEIRI).
The objectives of FEIRI are:
To describe the demographic and arterial characteristics of FMD and related diseases at a global scale and according to countries and/or ethnic origin
To identify environmental/ hormonal factors and exposures associated with the onset and progression of FMD
To evaluate the incidence and predictors of novel FMD lesions and complications
To provide evidence-based algorithms for the diagnosis and optimal management and follow-up of patients with FMD
To explore the commonalities and differences between FMD, SCAD and so-called atypical FMD (patients with multiple dissections and/or aneurysms without string-of-beads, focal stenosis or evidence of inherited arteriopathy)
To contribute to the unravelling of genetic, proteomic and molecular mechanisms underlying FMD and related diseases
Participation to the FEIRI study implies:
Collection of demographic and standard-of-care clinical data, both retrospectively (from the diagnosis of FMD to signature of the informed consent) and prospectively (on the occasion of standard-of-care follow-up).
Optional participation (both for centres and patients) to a biobank implying collection of blood, urine and, in rare cases of intervention, tissue samples for genomic and proteomic analysis and identification of diagnostic and prognostic biomarkers of FMD.
Participants will be enrolled in centres from over 20 countries in Europe and beyond.
- Conditions
- Fibromuscular Dysplasia
- Being tested
- Genetic dissection of Fibromuscular Dysplasia, Search for diagnostic and prognostic biomarkers of Fibromuscular Dysplasia
- Medical subject headings
- Fibromuscular Dysplasia
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
Genetic dissection of Fibromuscular DysplasiaGenetic
Blood sampling for genetic analysis aiming at unraveling the genetic basis of Fibromuscular Dysplasia
Search for diagnostic and prognostic biomarkers of Fibromuscular DysplasiaOther
Blood/urine and in rare cases tissue sampling aiming at identifying biomarkers of Fibromuscular Dysplasia
| Study group | Role | What they receive |
|---|---|---|
| Cohort of patients with Fibromuscular Dysplasia | Other | Intervention consists in blood/urine sampling Receives: Genetic: Genetic dissection of Fibromuscular Dysplasia; Other: Search for diagnostic and prognostic biomarkers of Fibromuscular Dysplasia |
What is being measured
The primary outcome is the main question the study is designed to answer.
Wide-scale analysis of characteristics and progression of Fibromuscular Dysplasia
Wide-scale analysis of baseline clinical characteristics and predictors of evolution/complications of Fibromuscular Dysplasia
Measured: 10 years
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted18 Mar 2021
- Study start11 Mar 2021
- Primary completion31 Dec 2022 (estimated)
- Study completion10 Mar 2031 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Fibromuscular DysplasiaStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase N/A
- Primary purpose
- Diagnosis
- Allocation
- Not applicable
- Intervention model
- Single group
- Model description
- The study is interventional because it requires blood/urine sampling.
- Masking
- None (open label)
- Enrolment
- 5,000 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Cliniques universitaires Saint-Luc- Université Catholique de Louvain
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, PERSU Alexandre, Cliniques universitaires Saint-Luc- Université Catholique de Louvain
- Investigators
- Alexandre Persu, MD-PhD, Principal investigator, Cliniques universitaires Saint-Luc- Université Catholique de Louvain
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT04804683
- Sponsor's protocol ID
- 2015/28AOU/464
- Acronym
- FEIRI
- Status last verified
- May 2022
- First submitted
- 15 Mar 2021
- Last updated
- 5 May 2022
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No