ID
38549
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)
- 10/6/19 10/6/19 -
- 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
Common CRF: Medical Conditions
- StudyEvent: ODM
Description
Cardiac Conditions
Alias
- UMLS CUI-1
- C0018799
Description
Heart Diseases, Sequence Number
Data type
integer
Alias
- UMLS CUI [1,1]
- C0018799
- UMLS CUI [1,2]
- C2348184
Description
Heart Diseases
Data type
text
Alias
- UMLS CUI [1]
- C0018799
Description
Heart Diseases, Reported Term
Data type
text
Alias
- UMLS CUI [1,1]
- C0018799
- UMLS CUI [1,2]
- C2826302
Description
Heart Diseases, Medical Dictionary for Regulatory Activities Terminology (MedDRA)
Data type
text
Alias
- UMLS CUI [1,1]
- C0018799
- UMLS CUI [1,2]
- C1140263
Description
Heart Diseases, MedDRA Low Level Term Code
Data type
text
Alias
- UMLS CUI [1,1]
- C0018799
- UMLS CUI [1,2]
- C3898442
Description
Heart Diseases, Code, Failed
Data type
text
Alias
- UMLS CUI [1,1]
- C0018799
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
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Common CRF: Medical Conditions
- StudyEvent: ODM
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C2826302 (UMLS CUI [1,2])
C1140263 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])