Effects of Sodium Nitrate on Blood Flow in Becker Muscular Dystrophy
Becker Muscular Dystrophy
About this trial
This is an interventional other trial for Becker Muscular Dystrophy
Eligibility Criteria
Inclusion Criteria:
- Men 15-55 years of age with a pre-existing diagnosis of Becker Muscular Dystrophy by a clinical neurologist (based on clinical criteria plus previous muscle biopsy analysis and/or DNA analysis).
Exclusion Criteria:
- Any evidence of cardiopulmonary disease by history or by physical examination
- History of hypertension or blood pressure averaging ≥140/90 mmHg
- Diabetes mellitus or other systemic illness
- Heart failure by clinical exam, elevated BNP, or heart failure medication
- Serum creatinine ≥ 1.5 mg/dL
- Any history of substance abuse (including alcohol)
- Any history of psychiatric illness
Sites / Locations
- Cedars-Sinai Heart Institute
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Experimental
No Intervention
Experimental
Placebo Comparator
Experimental
Sodium Nitrate
Baseline
Dose-escalation trial
Placebo-control trial
Increased exercise intensity
Patients will ingest a single oral dose of sodium nitrate (~8.4 mmol)
This is a baseline study visit, which will serve to assess inclusion and exclusion criteria, as well as provide untreated measurments of skeletal muscle blood flow and perfusion.
This is an optional study visit, where subjects will ingest twice the dose of sodium nitrate (~16.8 mmol).
This is an optional study visit, where patients will ingest a placebo.
This is an optional study visit, where patients will be asked to repeat all of the blood flow assessments, but the exercise intensity will be increased.