ID
38543
Description
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
Keywords
Versions (2)
- 9/29/19 9/29/19 -
- 10/24/19 10/24/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
October 24, 2019
DOI
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License
Creative Commons BY-NC 3.0
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Sumatriptan and Naproxen Sodium for Acute Treatment of Migraine Attacks; NCT00792636
Drug Dispensing / Return Information
- StudyEvent: ODM
Description
Drug Dispensing
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0947323
Description
Experimental drug, Dispensing medication
Data type
text
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0947323
Description
Experimental drug, Dispensing medication, Date in time
Data type
date
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0947323
- UMLS CUI [1,3]
- C0011008
Description
Experimental drug, Containers, Numbers
Data type
integer
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0237753
Similar models
Drug Dispensing / Return Information
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C0947323 (UMLS CUI-2)
C0947323 (UMLS CUI [1,2])
C0947323 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C0180098 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,3])