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Pruritus Visual Analogue Scale (VAS) Week 38 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Week 38

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Week 38.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Day 1 Week 8 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Day 1 Week 8

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Day 1 Pre-Infusion.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Week 4 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Week 4

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Week 4.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Week 12 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Week 12

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Week 12.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Week 28 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Week 28

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Week 28.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Week 16 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Week 16

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Week 16.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Week 24 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Week 24

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Week 24.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Week 20 Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Week 20

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Week 20.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Pruritus Visual Analogue Scale (VAS) Day 1 Pre-Infusion Mepolizumab HES NCT00086658 - Pruritus Visual Analogue Scale (VAS) Day 1 Pre-Infusion

- 5/6/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Assessment using visual analog scale Pruritus
Study part: Pruritus Visual Analogue Scale (VAS) Day 1 Pre-Infusion.A Phase 2 Multicenter, Double-blind, Placebo-controlled, Study to to Evaluate the Corticosteroid- sparing effects of Mepolizumab in Subjects with Hypereosinophilic Syndromes (HES) and Evaluate Efficacy and Safety of Mepolizumab in Controlling the Clinical Signs and Symptoms of subjects with HES Patient Level Data: Study Listed on ClinicalStudyDataRequest.com. Sponsor: GlaxoSmithKline. Study ID: 100185, Clinical Study ID:MHE100185.

Visual analogue scale CRFs Multiple Sclerosis Tysabri NCT00027300

- 30/1/17 - 1 formulario, 1 itemgroup, 2 items, 1 idioma
Itemgroup: Visual analogue scale
The purpose of this study is to determine the safety and efficacy of natalizumab in the treatment of individuals who have been diagnosed with relapsing remitting multiple sclerosis (MS). It is hoped that natalizumab will prevent certain types of white blood cells from moving out of the bloodstream into organs, including the brain, that are being damaged by autoimmune disease (a disease in which the body's own immune system attacks certain organs). These white blood cells are thought to cause inflammation that can result in lesions (small areas of damage) in the brain. These lesions are thought to be the cause of relapses and disability in MS. Documentation process: This form is to be obtained in Baseline Week 0, week 24, week 52, week 76, week 104, week 120, week 128 and Premature Study Withdrawl.

DWG-Register VAS Rückenschmerzen - Fragen zur Beeinträchtigungen durch Rückenschmerzen (VAS)

- 3/6/16 - 1 formulario, 1 itemgroup, 18 items, 1 idioma
Itemgroup: Visual analog Scale for back pain
Deutsche Wirbelsäulen Gesellschaft DWG-Register, http://www.dwg.org

Riliva_CRF_EudraCT - Nr. 2012-000108-13-Study termination DRKS00004652 - Riliva_CRF_EudraCT - Nr. 2012-000108-13-Study termination

- 11/11/15 - 1 formulario, 1 itemgroup, 4 items, 2 idiomas
Itemgroup: Study termination
Study description: Study documentation part- Study termination. This is a phase II multicenter trial with Rivaroxaban in the treatment of livedoid vasculopathy assessing the pain on a visual analog scale (VAS). Principal Investigator PD Dr. Tobias Grge, University Hospital of Mnster. EudraCT - Nr. 2012-000108-13.

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