Spironolactone Versus Prednisolone in DMD
Raktažodžiai
Santrauka
apibūdinimas
Until recently, the only treatment shown to improve strength and preserve ambulation in DMD patients was the use of glucocorticoids, which are accompanied by significant side effects including obesity, cushingoid features, osteoporosis, and behavioral disturbances. Spironolactone is an aldosterone antagonist primarily used as a potassium sparing diuretic that is widely used in the pediatric population, with limited side-effects including gynecomastia and hyperkalemia. Recent studies by Dr. Rafael-Fortney have evaluated the effect of spironolactone treatment in several different mouse models of DMD. Her results show that treatment of these mice demonstrates increased muscle membrane stabilization while reducing the negative side-effects typically associated with standard of care glucocorticoids. This pilot study is designed to determine whether this commonly used medication, spironolactone, may have similar beneficial effects with a lower side effect profile and be applicable to a wider population of DMD patients.
The hypothesis for this controlled pilot trial is that spironolactone and prednisolone are of equal efficacy in improving skeletal muscle function over a 6-month period, and that spironolactone will be well tolerated in this patient population.
One outcome is that both drugs demonstrate equal efficacy in motor function. This would then serve as pilot data for a longer term study.
Datos
| Paskutinį kartą patikrinta: | 01/31/2020 |
| Pirmasis pateikimas: | 12/09/2018 |
| Numatytas registravimas pateiktas: | 12/12/2018 |
| Pirmas paskelbtas: | 12/16/2018 |
| Paskutinis atnaujinimas pateiktas: | 02/17/2020 |
| Paskutinis atnaujinimas paskelbtas: | 02/19/2020 |
| Faktinė studijų pradžios data: | 12/04/2018 |
| Numatoma pirminio užbaigimo data: | 11/30/2021 |
| Numatoma studijų užbaigimo data: | 11/30/2021 |
Būklė ar liga
Intervencija / gydymas
Drug: Spironolactone
Drug: Prednisolone
Fazė
Rankų grupės
| Ranka | Intervencija / gydymas |
|---|---|
| Experimental: Spironolactone Twelve subjects will be prescribed a standard clinical dose of spironolactone of 1 mg/kg/day. The spironolactone will be provided as suspension. | Drug: Spironolactone Spironolactone will be prescribed for 6 months, after which the family and primary care physician will determine to either remain on spironolactone or transfer to prednisolone. |
| Active Comparator: Prednisolone Twelve subjects will be prescribed a standard clinical dose of prednisolone of 0.75 mg/kg/day or weekend dosing of 5 mg/kg/day as per sites standard of care. The prednisolone will be provided will be provided as suspension. | Drug: Prednisolone Prednisolone will be prescribed for 6 months as the clinical standard of care. |
Tinkamumo kriterijai
| Amžius, tinkami studijuoti | 4 Years Į 4 Years |
| Tinkamos studijoms lytys | Male |
| Priima sveikus savanorius | Taip |
| Kriterijai | Inclusion Criteria: - Duchenne muscular dystrophy (DMD) patients ≥4 to ≤7 years of age - Clinical features of DMD that include proximal predominant weakness and/or gait disturbance - Presence of a truncating mutation of the DMD gene OR a muscle biopsy that demonstrates <5% dystrophin in the patient or an affected relative - Normal left ventricular ejection fraction by screening echocardiogram - Ability to cooperate for testing - No prior glucocorticoid treatment - No concomitant experimental therapies Exclusion Criteria: - Subject amenable to or currently being treated with eteplirsen - Hyperkalemia at screening - History of or ongoing renal failure (elevated creatinine, oliguria, anuria) - Hypersensitivity to spironolactone (rash, respiratory distress, arrhythmia, numbness or tingling of extremities) - Current treatment with an ACEi - Severe peptic ulcer disease or recent gastrointestinal perforations |
Rezultatas
Pirminės rezultatų priemonės
1. Efficacy: Change in time to complete a 100 meter timed test. [6 months]
2. Safety will be monitored through regular review of electrolytes. [6 months]
Antrinės rezultatų priemonės
1. Efficacy: Dynamometry score [6 months]
