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Randomized, Single Blind, Controlled Trial of Inhaled Glutathione Versus Placebo in Patients With Cystic Fibrosis
Cystic fibrosis (CF) is the most common inherited disease among the Caucasian population with considerable morbidity and reduced life expectancy. Excessive oxidants released by activated inflammatory cells and persisting infections are considered the main mechanism of damage of respiratory epithelium in CF.Glutathione (GSH) represents the first-line defence of the lung against oxidative stress-induced cell injury; however, a depletion of its levels has been observed in the airways of patients affected by CF. In vitro studies have showed that CFTR protein plays a pivotal role in transmembrane glutathione transport. Therapeutic approaches with inhaled GSH could improve the reduced lung antioxidant capacity in order to counterbalance the oxidant stress linked to the chronic airway inflammation and bacterial infection. Primary objective of the study is to investigate whether a 12 months treatment with inhaled GSH can improve airway obstruction in CF patients. Secondary objectives include the effects of GSH therapy on exercise capacity, body mass index (BMI), respiratory symptoms, quality of life, frequency of pulmonary exacerbations, hospital admissions, and antibiotic administration. Moreover the study will evaluate the effect of GSH therapy on markers of oxidative stress in exhaled breath condensate (EBC) and in serum, and on inflammatory markers on brushed nasal epithelial cells.
Details
| Lead sponsor | Serafino A. Marsico |
|---|---|
| Phase | Phase 3 |
| Status | UNKNOWN |
| Enrolment | 150 |
| Start date | 2010-06 |
| Completion | 2012-12 |
Conditions
- Cystic Fibrosis
Interventions
- Inhaled Reduced Glutathione
- Physiological solution
Primary outcomes
- Forced expiratory volume in one second (FEV1) percent — 12 months
Increase of at least 15% of the percent of forced expiratory volume in one second (FEV1) after GSH therapy compared to placebo
Countries
Italy