TY - JOUR ID - 240881 TI - Efficacy of Low-Dose Ciclesonide and Fluticasone Propionate for Mild to Moderate Persistent Asthma JO - TANAFFOS (Respiration) JA - RSPR LA - en SN - 1735-0344 AU - Jamaati, Hamidreza AU - Malekmohammad, Majid AU - Fahimi, Fanak AU - Najafi, Arvin AU - Hashemian, Seyed Mohammadreza AD - Tobacco Prevention and Control Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences,Tehran, Iran, AD - Tracheal Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran, AD - Chronic Respiratory Diseases Research Center, National Research Institute of Tuberculosis and Lung Diseases (NRITLD), Shahid Beheshti University of Medical Sciences, Tehran, Iran. Y1 - 2015 PY - 2015 VL - 14 IS - 1 SP - 1 EP - 9 KW - Asthma KW - Ciclesonide KW - Efficacy KW - Fluticasone Propionate DO - N2 - Background: The aim of this study was to compare the efficacy of ciclesonide (80 mg/day) and fluticasone propionate (200 mg/day) for mild to moderate persistent asthma. Materials and Methods: Female and male patients older than 12 years with a history of persistent bronchial asthma for at least 6 months were enrolled. Patients were eligible to enter into a 2-week run-in period before randomization (baseline) if they had received inhaled corticosteroids (fluticasone propionate 250 µg/day or equivalent) at a constant dose during the last 4 weeks before the run-in period. In order to enter into the double blind 18-week treatment period, patients had to have a forced expiratory volume in 1s (FEV1) of 61-90% of predicted and a decrease in FEV1 throughout the run-in period of more than 10%. Patients (n =230) were assigned to ciclesonide 80 mg once daily or fluticasone propionate 100 mg twice daily group. The primary outcome variable was change in FEV1 compared to its baseline value. Secondary outcome variables were asthma-specific quality of life and asthma control. Results: Both drugs significantly increased FEV1 and other lung function parameters compared to baseline (p < 0.0001, both groups, all variables). Progress in the percentage of days with no asthma symptoms and no use of rescue medication and asthma-specific quality of life were similar in the two treatment groups. Conclusion: Ciclesonide at a dose of 80 µg once daily can provide efficient maintenance therapy for mild to moderate persistent asthma. UR - https://www.tanaffosjournal.ir/article_240881.html L1 - https://www.tanaffosjournal.ir/article_240881_b3492f7fadcc12e65a903b36b54abf6f.pdf ER -