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Basic documentation B2 LeMLAR-Studie Lymphoma NCT01788189 - Basic documentation B2

- 2021-03-15 - 1 Formulär, 3 Item-grupper, 26 Dataelement, 1 Språk
Item-grupper: medical history, Inclusion Criteria, Exclusion Criteria
Study part: Basic documentation B2 LeMLAR-Studie. LeMLAR-Studie. Lenalidomide in conjunction with methotrexate, leucovorin, cytarabine and rituximab for the treatment of relapsed or refractory CD20-positive aggressive lymphomas: an open-label, multicenter phase I/II trial. Publication granted by Prof. Dührsen and provided by Claudia Ose, University clinic Essen, NCT01788189, Version 1.3-28.04.2013.doc.

GSK Study ID 100807 Fluticasone Propionate from SERETIDE™ (500/50) DISKUS™ and Budesonide from Symbicort (200/6) Turbuhaler in patients with severe Chronic Obstructive Pulmonary Disease. Subject Diary Card - Subject Diary Card

- 2017-10-10 - 1 Formulär, 3 Item-grupper, 48 Dataelement, 1 Språk
Item-grupper: Subject Diary Card, Subject Diary Card, Subject Diary Card Treatment Period 2
Randomised, open label, two period, crossover study to compare the steroid systemic exposure of Fluticasone Propionate (FP) from FP/Salmeterol (SALM) (500/50) DISKUS and Budesonide (BUD) from BUD/formoterol (FOR).(200/6) Turbuhaler in patients with severe Chronic Obstructive Pulmonary Disease. Primary objective:To compare the exposure of the inhaled steroid fluticasone propionate (FP) and budesonide following repeat dosing with SERETIDE DISKUS (500/50) one inhalation twice daily (b.i.d.) when compared with Symbicort Turbuhaler (200/6) two inhalations b.i.d. in a severe chronic pulmonary obstructive disease (COPD) population. Secondary objectives:To compare the pharmacokinetics of FP and budesonide following repeat dosing with SERETIDE DISKUS (500/50) one inhalation b.i.d. when compared with Symbicort Turbuhaler (200/6) two inhalations b.i.d. in a severe COPD population and to explore further the pharmacokinetics of FP and budesonide.

daily record card administration salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

- 2017-08-16 - 1 Formulär, 2 Item-grupper, 7 Dataelement, 1 Språk
Item-grupper: administrative data, next clinic visit
Study ID: 100470 Clinical Study ID: SCO100470 Study Title: A multicentre, randomised, double-blind, parallel group, 24 week study to compare the effect of salmeterol/fluticasone propionate combination product 50/250mcg, with salmeterol 50mcg both delivered twice daily via DISKUS®/ACCUHALER® inhaler on lung function and dyspnoea in subjects with Chronic Obstructive Pulmonary Disease (COPD). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor:GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone propionate/salmeterol Trade Name: Serevent Study Indication: Pulmonary Disease, Chronic Obstructive

daily record card documentation salmeterol/fluticasone propionate combination compared to salmeterol on COPD 100470

- 2017-08-16 - 1 Formulär, 4 Item-grupper, 19 Dataelement, 1 Språk
Item-grupper: administrative data, documentation of health status, symptoms of COPD, worksheet
Study ID: 100470 Clinical Study ID: SCO100470 Study Title: A multicentre, randomised, double-blind, parallel group, 24 week study to compare the effect of salmeterol/fluticasone propionate combination product 50/250mcg, with salmeterol 50mcg both delivered twice daily via DISKUS®/ACCUHALER® inhaler on lung function and dyspnoea in subjects with Chronic Obstructive Pulmonary Disease (COPD). Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: N/A Sponsor:GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: fluticasone propionate/salmeterol Trade Name: Serevent Study Indication: Pulmonary Disease, Chronic Obstructive

Baseline RICH study NCT02669589

- 2016-06-12 - 1 Formulär, 21 Item-grupper, 234 Dataelement, 1 Språk
Item-grupper: Patient Information, Patient Data, Kidney Disease: Improving Global Outcomes (KDIGO), Renal function, Neurologic dysfunction, Pulmonary dysfunction, Cardiovascular disorder, Gastrointestinal dysfunction, Other organ dysfunction, Main diagnosis for admission, Pre-existing illness, Premedication, Glasgow Coma Scale, Mechanical ventilation, Catecholamine and inotropic therapy, Vital signs, Concomitant medication, Laboratory Parameters and Blood Gas Analysis, Fluid balance, Transfusion, Microbiology
NCT02669589 EudraCT-Nr. 2014-004854 [Titel anhand dieser ISBN in Citavi-Projekt übernehmen] -33 REGIONAL CITRATE VERSUS SYSTEMIC HEPARIN ANTICOAGULATION FOR CONTINUOUS RENAL REPLACEMENT THERAPY IN CRITICALLY ILL PATIENTS WITH ACUTE KIDNEY INJURY Study Chair: Alexander Zarbock, MD University Hospital Muenster

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