ID

38555

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. 10/9/19 10/9/19 -
  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 : Other Previous Treatment for Migraine

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
Other Previous Treatment for Migraine
Description

Other Previous Treatment for Migraine

Alias
UMLS CUI-1
C0149931
UMLS CUI-2
C1514463
UMLS CUI-3
C0205394
Other medication, specify
Description

Migraine Disorders, Prior Therapy, Other

Data type

text

Alias
UMLS CUI [1,1]
C0149931
UMLS CUI [1,2]
C1514463
UMLS CUI [1,3]
C0205394
Previous use of medication(s) for the acute treatment of migraine
Description

Migraine Disorders, Prior Therapy

Data type

text

Alias
UMLS CUI [1,1]
C0149931
UMLS CUI [1,2]
C1514463

Similar models

Common CRF : Other Previous Treatment for Migraine

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
Other Previous Treatment for Migraine
C0149931 (UMLS CUI-1)
C1514463 (UMLS CUI-2)
C0205394 (UMLS CUI-3)
Migraine Disorders, Prior Therapy, Other
Item
Other medication, specify
text
C0149931 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
C0205394 (UMLS CUI [1,3])
Item
Previous use of medication(s) for the acute treatment of migraine
text
C0149931 (UMLS CUI [1,1])
C1514463 (UMLS CUI [1,2])
Code List
Previous use of medication(s) for the acute treatment of migraine
CL Item
Currently using (during the past 3 months) (1)
CL Item
Used at any time in past (but not within the past 3 months) (2)

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