Myotonic Dystrophy Clinical Trial
— STAROfficial title:
Sleep Breathing Disorders, a Main Trigger for Cardiac ARythmias in Type I Myotonic Dystrophy ?
NCT number | NCT02375087 |
Other study ID # | "STAR" |
Secondary ID | |
Status | Completed |
Phase | |
First received | |
Last updated | |
Start date | May 20, 2014 |
Est. completion date | July 1, 2017 |
Verified date | January 2020 |
Source | University Hospital, Grenoble |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
Up to one-third of patients with myotonic dystrophy type 1 die suddenly mainly from arrhythmias. Sleep apnea is prevalent in myotonic dystrophy (DM1) patients. Among the serious complications from sleep apnea, the most alarming are arrhythmias and sudden cardiac death (SCD). Diagnosis of sleep apnea using simple tools in ambulatory cardiology practice may improve therapy of cardiac arrhythmias in patients with DM1
Status | Completed |
Enrollment | 73 |
Est. completion date | July 1, 2017 |
Est. primary completion date | July 1, 2017 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients suffering from myotonic dystrophy (DM1) - DM1 patients participating in the clinical cohorts of Grenoble, Saint-Etienne and Montpellier. - Patients implanted or not with pacing devices or cardioverter-defibrillator (ICD). - Patients treated or not by non invasive ventilation (NIV) at home. As a majority, of the patients with DM1 are poorly adherent with NIV they continue to exhibit significant desaturation during night. Truly compliant patients (mean daily duration>6/h night) will be studied as a predefined subgroup to assess the protective effect of NIV for suppressing oxygen desaturations and avoiding occurrence of nocturnal arrhythmias. Exclusion Criteria: - Patients who have had an acute episode of respiratory failure in the previous month - Incapacitated patients in accordance with article L 1121-6 of the public health code |
Country | Name | City | State |
---|---|---|---|
France | CHU | Grenoble |
Lead Sponsor | Collaborator |
---|---|
University Hospital, Grenoble |
France,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Cardiac arythmia related to hypoxia and respiratory events | Ambulatory at home concurrent assessment of arrhythmias and sleep breathing disorders by a multi-modal ECG Holter (Vista O2; Novacor, Rueil Malmaison, FranceTM). We will record seven consecutive nights at home to increase the sensitivity and the number of abnormal rhythmic events available for analysis. One night full polysomnography followed by Multiple sleep latency tests | 7days | |
Secondary | A temporal link between Sleep desordered breathing events and the developpement of arrythmias | More specifically the occurrence of arrhythmias will be correlated with the severity of oxygen desaturation | 7 days | |
Secondary | To assess during the entire night the increase in sympathetic activity (LF/HF ratio) in response to abnormal respiratory events during sleep and the relationship between sympathetic activity and prevalence of arrhythmias | 7 days | ||
Secondary | To compare arrhythmias prevalence in REM and non REM sleep | 7 days | ||
Secondary | To see whether a high adherence to non invasive ventilation (>6hours/night) and the suppression of oxygen desaturation is associated with a lower prevalence of arrhythmias | 7 days |
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