ID
38563
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)
- 24-10-19 24-10-19 -
- 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
End of Study
- StudyEvent: ODM
Beschrijving
Date of Visit/Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Beschrijving
Pharmacogenetic (PGx) Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Beschrijving
Pharmacogenetic Test, Informed Consent, Withdraw
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
Beschrijving
Pharmacogenetic Test, Informed Consent, Withdraw, Date in time
Datatype
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
- UMLS CUI [1,4]
- C0011008
Beschrijving
Pharmacogenetic Test, Blood specimen, Destruction, Request
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Beschrijving
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Beschrijving
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
- UMLS CUI [1,5]
- C0566251
Beschrijving
Status of Treatment Blind
Alias
- UMLS CUI-1
- C2347038
- UMLS CUI-2
- C0449438
Beschrijving
Blinded Clinical Study, Subject Unblinding Event Record
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
Beschrijving
Blinded Clinical Study, Subject Unblinding Event Record, Date in time
Datatype
date
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0011008
Beschrijving
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Beschrijving
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Datatype
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Beschrijving
Medical Device Question
Alias
- UMLS CUI-1
- C0025080
- UMLS CUI-2
- C1522634
Beschrijving
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Beschrijving
Study Conclusion
Alias
- UMLS CUI-1
- C0008976
- UMLS CUI-2
- C1707478
Beschrijving
Completion Status, Date in time; Withdraw, Date in time
Datatype
date
Alias
- UMLS CUI [1,1]
- C0805732
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C2349954
- UMLS CUI [2,2]
- C0011008
Beschrijving
Patient withdrawn from trial
Datatype
boolean
Alias
- UMLS CUI [1]
- C0422727
Beschrijving
Patient withdrawn from trial, Reason and justification, Primary
Datatype
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Beschrijving
Patient withdrawn from trial, Reason and justification, Primary
Datatype
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Beschrijving
Clinical study case, Investigator Signature
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C2346576
Similar models
End of Study
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C2985720 (UMLS CUI-2)
C2985720 (UMLS CUI [2])
C0021430 (UMLS CUI-2)
C2349954 (UMLS CUI-3)
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0021430 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0178913 (UMLS CUI [1,2])
C1948029 (UMLS CUI [1,3])
C1272683 (UMLS CUI [1,4])
C0566251 (UMLS CUI [1,5])
C0449438 (UMLS CUI-2)
C3897431 (UMLS CUI [1,2])
C3897431 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,3])
C3897431 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C3897431 (UMLS CUI [1,2])
C0566251 (UMLS CUI [1,3])
C1522634 (UMLS CUI-2)
C1551358 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,2])
C0008976 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C2349954 (UMLS CUI [2,1])
C0011008 (UMLS CUI [2,2])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C0566251 (UMLS CUI [1,2])
C0205225 (UMLS CUI [1,3])
C2346576 (UMLS CUI [1,2])