ID
34427
Descripción
Study ID: 101998 Clinical Study ID: 101998 Study Title: A randomized, double-blind, parallel group, placebo-controlled, single-attack evaluation of the efficacy and tolerability of TREXIMA™ (sumatriptan 85mg/naproxen sodium 500mg)* tablets vs placebo when administered during the mild pain phase of a migraine Patient Level Data Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier Sponsor GlaxoSmithKline Collaborators N/A Phase Phase 3 Study Recruitment Status Completed Generic Name sumatriptan Trade Name Imitrex ,Imiject ,Imigran Study Indication Migraine Disorders The purpose of this form is to record any previous treatment for migraine, the subject has taken. It should be filled out at the screening visit.
Palabras clave
Versiones (2)
- 13/1/19 13/1/19 -
- 17/1/19 17/1/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
17 de enero de 2019
DOI
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Licencia
Creative Commons BY-NC 3.0
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Efficacy and Tolerability of TREXIMA Tablets vs. Placebo During Mild Migraine Study ID 101998
Previous Migraine Treatment
- StudyEvent: ODM
Descripción
Previous Migraine Treatment
Alias
- UMLS CUI-1
- C0149931
- UMLS CUI-2
- C1514463
Descripción
NSAIDs are not containing naproxen (aspirin, ibuprofen, Advil, Motrin, etc.) Other Prescription NSAIDs are not containing naproxen or COX-2 inhibitors (Relafen, Feldene, Indocinx, Orudis, Voltaren, Daypro, Toradol, etc.
Tipo de datos
integer
Alias
- UMLS CUI [1]
- C2347852
- UMLS CUI [2]
- C2826808
Descripción
Tick one for each medication/medication category Currently using: during the past 3 months Used at any time in the past: but not within the past 3 months
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C0149931
- UMLS CUI [1,2]
- C1514463
- UMLS CUI [1,3]
- C0013227
Descripción
For any medication used
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1274040
- UMLS CUI [1,2]
- C0013227
- UMLS CUI [1,3]
- C0242428
Descripción
Best Medication Response
Alias
- UMLS CUI-1
- C2986560
- UMLS CUI-2
- C0013227
Similar models
Previous Migraine Treatment
- StudyEvent: ODM
C1514463 (UMLS CUI-2)
C2826808 (UMLS CUI [2])
C1514463 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0013227 (UMLS CUI [1,2])
C0242428 (UMLS CUI [1,3])
C0013227 (UMLS CUI-2)
C0013227 (UMLS CUI [1,2])
Sin comentarios