ID
38553
Beschrijving
Study ID: 110948 Clinical Study ID: 110948 Study Title: Assessment of the effect of sumatriptan and naproxen sodium combination tablet, sumatriptan tablet, and naproxen sodium tablet treatment on blood pressure when administered intermittently for six months for the acute treatment of migraine attacks, with or without aura, in adults Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00792636 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 4 Study Recruitment Status: Completed Generic Name: sumatriptan and naproxen sodium combination tablet Trade Name: sumatriptan tablet, naproxen sodium tablet Study Indication: Migraine Disorders
Trefwoorden
Versies (2)
- 09-10-19 09-10-19 -
- 24-10-19 24-10-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
24 oktober 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Sumatriptan and Naproxen Sodium for Acute Treatment of Migraine Attacks; NCT00792636
Common CRF : Drug Dispensing/Return Information
- StudyEvent: ODM
Beschrijving
Drug Dispensing/Return Information
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0947323
- UMLS CUI-3
- C0332156
Beschrijving
Experimental drug, Dispensing medication, Containers
Datatype
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0947323
- UMLS CUI [1,3]
- C0180098
Beschrijving
Experimental drug, Dispensing medication, Date in time
Datatype
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0947323
- UMLS CUI [1,3]
- C0011008
Beschrijving
Experimental drug, Containers, Numbers
Datatype
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0237753
Similar models
Common CRF : Drug Dispensing/Return Information
- StudyEvent: ODM
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C0947323 (UMLS CUI-2)
C0332156 (UMLS CUI-3)
C0947323 (UMLS CUI [1,2])
C0180098 (UMLS CUI [1,3])
C0947323 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0180098 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])