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

  1. 10/6/19 10/6/19 -
  2. 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

Administrative Data
Description

Administrative Data

Alias
UMLS CUI-1
C1320722
Site
Description

Study Site

Data type

text

Alias
UMLS CUI [1]
C2825164
Patient
Description

Patient name

Data type

text

Alias
UMLS CUI [1]
C1299487
Patient No
Description

Patients, Identification number

Data type

integer

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C1300638
Cardiac Conditions
Description

Cardiac Conditions

Alias
UMLS CUI-1
C0018799
Sequence Number
Description

Heart Diseases, Sequence Number

Data type

integer

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C2348184
Specific Condition
Description

Heart Diseases

Data type

text

Alias
UMLS CUI [1]
C0018799
Modified Term
Description

Heart Diseases, Reported Term

Data type

text

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C2826302
MedDRA Synonym
Description

Heart Diseases, Medical Dictionary for Regulatory Activities Terminology (MedDRA)

Data type

text

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C1140263
MedDRA lower level term code
Description

Heart Diseases, MedDRA Low Level Term Code

Data type

text

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C3898442
Failed coding
Description

Heart Diseases, Code, Failed

Data type

text

Alias
UMLS CUI [1,1]
C0018799
UMLS CUI [1,2]
C0805701
UMLS CUI [1,3]
C0231175

Similar models

Common CRF: Medical Conditions

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Administrative Data
C1320722 (UMLS CUI-1)
Study Site
Item
Site
text
C2825164 (UMLS CUI [1])
Patient name
Item
Patient
text
C1299487 (UMLS CUI [1])
Patients, Identification number
Item
Patient No
integer
C0030705 (UMLS CUI [1,1])
C1300638 (UMLS CUI [1,2])
Item Group
Cardiac Conditions
C0018799 (UMLS CUI-1)
Heart Diseases, Sequence Number
Item
Sequence Number
integer
C0018799 (UMLS CUI [1,1])
C2348184 (UMLS CUI [1,2])
Heart Diseases
Item
Specific Condition
text
C0018799 (UMLS CUI [1])
Heart Diseases, Reported Term
Item
Modified Term
text
C0018799 (UMLS CUI [1,1])
C2826302 (UMLS CUI [1,2])
Heart Diseases, Medical Dictionary for Regulatory Activities Terminology (MedDRA)
Item
MedDRA Synonym
text
C0018799 (UMLS CUI [1,1])
C1140263 (UMLS CUI [1,2])
Heart Diseases, MedDRA Low Level Term Code
Item
MedDRA lower level term code
text
C0018799 (UMLS CUI [1,1])
C3898442 (UMLS CUI [1,2])
Heart Diseases, Code, Failed
Item
Failed coding
text
C0018799 (UMLS CUI [1,1])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])

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