All clinical trials on the European Union Clinical Trials Register (EUCTR) must report their results in the registry within a year of completion. This site tracks who's doing this and who isn't. Learn more »
These trials completed more than 12 months ago and should have reported results. Some have, some have not.
These trials are not yet due to report results: some are ongoing, some completed within the past 12 months.
These trials have problematic data on the registry. Details why »
Status | Trial ID | Title | Completion date | Category |
---|---|---|---|---|
Reported results | 2004-000288-89 | A 24 week, double blind, randomized study to investigate the effect of 500 µg Roflumilast tablets once daily versus placebo on parameters indicative of hyperinflation in patients with chronic obstruct... | 2005-11-08 | due-trials |
Completed, but no date, and reported results | 2004-000492-33 | Healing of patients suffering from gastroesophageal reflux esophagitis grade C-D according to Los Angeles classification after treatment with pantoprazole-magnesium dihydrate 80 mg o.d. in comparison ... | bad-data | |
Reported results | 2004-000493-32 | Healing of patients suffering from gastroesophageal reflux esophagitis grade A-D according to Los Angeles classification after treatment with pantoprazole-magnesium dihydrate 80 mg o.d. in comparison ... | 2005-02-01 | due-trials |
Completed, but no date, and reported results | 2004-000825-31 | Comparison of ciclesonide (80 µg or 160 µg once daily in the evening) and fluticasone propionate (100 µg twice daily in the morning and evening) in pediatric asthma patients | bad-data | |
Reported results | 2004-001065-18 | Morning versus evening administration of 500µg Roflumilast once dailyfor 6 weeks in patients with asthma. | 2005-07-07 | due-trials |
Reported results | 2004-001072-39 | Comparison of Ciclesonide (80 µg Once Daily in the Evening) and Fluticasone propionate (100 µg Twice Daily) in Patients with Mild to Moderate Asthma | 2006-01-09 | due-trials |
Reported results | 2004-001681-40 | Comparison of inhaled ciclesonide (640 g/day) and fluticasone propionate (1000 g/day) in patients with moderate and severe persistent asthma. | 2005-11-30 | due-trials |
Reported results | 2004-001838-16 | Efficacy and safety of a fixed combination of ciclesonide and formoterol once or twice daily in the treatment of persistent asthma A randomized, double-blind, placebo-controlled, parallel-group, multi... | 2005-06-28 | due-trials |
Reported results | 2004-002983-80 | Comparison of the Efficacy of a Fixed Combination of Ciclesonide and Formoterol versus a Fixed Combination of Fluticasone and Salmeterol | 2005-08-02 | due-trials |
Not reported | 2004-004442-40 | 500µg roflumilast once daily in combination with 50µg salmeterol twice daily versus 50µg salmeterol twice daily alone over 52 weeks in patients with COPD. | 2005-06-15 | due-trials |
Reported results | 2004-004708-19 | A dose range finding study of formoterol administered once daily in the evening in combination with ciclesonide using the UltrahalerTM versus monotherapy of each drug in asthmatic patients | 2006-01-26 | due-trials |
Reported results | 2004-004806-25 | Evaluation of the complete remission rates in patients with symptomatic non-erosive reflux disease (NERD) or erosive gastroesophageal reflux disease (GERD) treated with pantoprazole 40 mg o.d. over 4... | 2007-04-13 | due-trials |
Reported results | 2005-000711-10 | Determination of the performance characteristics of ReQuestTM in Practice in the stepped down management of GORD | 2006-03-31 | due-trials |
Reported results | 2005-001242-17 | Efficacy and Safety – Study by ALTANA on Ciclesonide in Pre-school Asthma Patients | 2007-05-31 | due-trials |
Reported results | 2005-001386-34 | Effect of Ciclesonide (320 µg/day) vs. Fluticasone Propionate (375 µg/day) vs. Placebo on Short-term Linear Growth Rate and HPA-axis Function in Prepubertal Children with Mild Asthma A double-blind... | 2006-06-21 | due-trials |
Reported results | 2005-001497-27 | Effect of pantoprazole on sleep-related breathing disorders | 2007-01-24 | due-trials |
Not reported | 2005-001740-24 | A Dose Range Finding Study of Formoterol Fumarate administered twice daily using the Ultrahaler™ in Patients with Asthma | 2006-02-03 | due-trials |
Reported results | 2005-002163-84 | Comparison of the Efficacy and Safety of 160 mcg Ciclesonide Administered Once Daily in the Evening with ot without Different Spacer Types in Patients with Asthma | 2006-05-10 | due-trials |
Reported results | 2005-003485-42 | Treatment response in patients with symptoms due to gastroesophageal reflux disease either with or without esophagitis treated with pantoprazole sodium 40 mg o.d. over 8 weeks | 2007-08-14 | due-trials |
Reported results | 2005-003937-42 | Effect of roflumilast on exacerbation rate in patients with COPD A 52 weeks, double-blind study with 500 mcg roflumilast once daily versus placebo | 2008-09-25 | due-trials |
Reported results | 2005-003938-18 | Effect of roflumilast on exacerbation rate in patients with COPD. A 52 weeks, double-blind study with 500 mcg roflumilast once daily versus placebo | 2008-08-14 | due-trials |
Reported results Terminated | 2005-004856-11 | Symptom reduction in hospitalized patients suffering from symptomatic non-erosive or erosive gastroesophageal reflux disease treated with pantoprazole 20 or 40 mg o.d. for 7 days | 2007-06-29 | due-trials |
Reported results | 2005-005080-28 | Effect of roflumilast in COPD patients treated with salmeterol. A 24 week, double blind study with 500 mcg roflumilast once daily versus placebo | 2008-02-12 | due-trials |
Reported results | 2006-000803-40 | A comparative study of inhaled ciclesonide versus placebo in children with asthma (RAINBOW) | 2007-11-29 | due-trials |
Reported results | 2006-000926-30 | Investigation of clinical endpoints for treatment-induced gastroesophageal reflux disease (GERD) symptom changes | 2007-03-29 | due-trials |
Reported results | 2006-002214-35 | Free, not protein-bound concentrations of budesonide in subcutaneous adipose tissue, muscle tissue, and serum after oral inhalation via Turbohaler® | 2006-08-16 | due-trials |
Not reported Terminated | 2006-002777-42 | Endoscopic healing and tolerability of Soraprazan 20 mg qd compared to Soraprazan 10 mg qd and to Esomeprazole 40 mg qd in patients suffering from GERD Grade A-D (LA classification) | 2007-01-31 | due-trials |
Not reported Terminated | 2006-002779-42 | Symptom relief and tolerability of Soraprazan 20 mg qd and Soraprazan 10 mg qd compared to Esomeprazole 20 mg qd in patients with non-erosive gastroesophageal reflux disease (NERD) | 2007-01-31 | due-trials |
Reported results | 2006-004508-37 | Effect of roflumilast in COPD patients treated with tiotropium. A 24-week, double-blind study with 500 g roflumilast once daily versus placebo. | 2008-07-07 | due-trials |
Reported results | 2006-004882-32 | Evaluation of clinical endpoints for treatment-induced changes in GERD-related symptoms | 2009-03-13 | due-trials |