Fabry Disease Clinical Trials

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Natural History of Cardiac Rhythm and Conduction Disorders in Patients With Fabry Disease Evaluated by Long-Term Implantable Holter ECG

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The main objective is to assess the occurrence of cardiac arrhythmias and conduction disorders during a three-year follow-up using implantable Holter ECG monitoring in 40 patients with Fabry disease. The secondary objectives are to analyze the correlations of these anomalies with changes in cardiac MRI and echocardiographic parameters as biological parameters and overall severity of the disease assessed by MSSI.

Eligibility
Participation Requirements
Sex: Male
Minimum Age: 18
Healthy Volunteers: f
View:

• Male patient

• Age greater than or equal to 18 years on the day of inclusion

• Presence of a morbid mutation for MF

• Signature of the informed consent form

• Absence of significant valve disease, verified on medical file (absence stenosis or regurgitation \<2+ in color Doppler on a scale 1 to 4+ by extension of the jet)

• No history of known or documented myocardial infarction nor CAD

• No pacemaker or ICD

• no history of AF, NSVT, high-degree AV block

• Correct echogenicity

• No treatment by corticosteroid or immunosuppressive drugs

• creatinine clearance \>/= 30 Ml/mn

• LVEF ≥ 50% by ultrasound and / or MRI

• No contraindication to MRI (or claustrophobia) and gadolinium injection

• Affiliation to the French social security insurance

Locations
Other Locations
France
20 Rue Leblanc, HEGP/PARCC, 75015 Paris
RECRUITING
Paris
Contact Information
Primary
Albert HAGEGE, Dr
albert.hagege@inserm.fr
0156093713
Time Frame
Start Date: 2021-05-05
Estimated Completion Date: 2029-04-30
Participants
Target number of participants: 40
Treatments
Other: ONE
One single group of patients
Related Therapeutic Areas
Sponsors
Leads: Institut National de la Santé Et de la Recherche Médicale, France

This content was sourced from clinicaltrials.gov