ID
38563
Descripción
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
Palabras clave
Versiones (2)
- 24/10/19 24/10/19 -
- 24/10/19 24/10/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
24 de octubre de 2019
DOI
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Licencia
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
Descripción
Date of Visit/Assessment
Alias
- UMLS CUI-1
- C1320303
- UMLS CUI-2
- C2985720
Descripción
Pharmacogenetic (PGx) Research Withdrawal of Consent
Alias
- UMLS CUI-1
- C2347500
- UMLS CUI-2
- C0021430
- UMLS CUI-3
- C2349954
Descripción
Pharmacogenetic Test, Informed Consent, Withdraw
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
Descripción
Pharmacogenetic Test, Informed Consent, Withdraw, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0021430
- UMLS CUI [1,3]
- C2349954
- UMLS CUI [1,4]
- C0011008
Descripción
Pharmacogenetic Test, Blood specimen, Destruction, Request
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347500
- UMLS CUI [1,2]
- C0178913
- UMLS CUI [1,3]
- C1948029
- UMLS CUI [1,4]
- C1272683
Descripción
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Tipo de datos
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
Descripción
Pharmacogenetic Test, Blood specimen, Destruction, Request, Reason and justification
Tipo de datos
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
Descripción
Status of Treatment Blind
Alias
- UMLS CUI-1
- C2347038
- UMLS CUI-2
- C0449438
Descripción
Blinded Clinical Study, Subject Unblinding Event Record
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
Descripción
Blinded Clinical Study, Subject Unblinding Event Record, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0011008
Descripción
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Descripción
Blinded Clinical Study, Subject Unblinding Event Record, Reason and justification
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C2347038
- UMLS CUI [1,2]
- C3897431
- UMLS CUI [1,3]
- C0566251
Descripción
Medical Device Question
Alias
- UMLS CUI-1
- C0025080
- UMLS CUI-2
- C1522634
Descripción
Pregnancy Information
Alias
- UMLS CUI-1
- C0032961
- UMLS CUI-2
- C1533716
Descripción
Study Conclusion
Alias
- UMLS CUI-1
- C0008976
- UMLS CUI-2
- C1707478
Descripción
Completion Status, Date in time; Withdraw, Date in time
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C0805732
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [2,1]
- C2349954
- UMLS CUI [2,2]
- C0011008
Descripción
Patient withdrawn from trial
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C0422727
Descripción
Patient withdrawn from trial, Reason and justification, Primary
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Descripción
Patient withdrawn from trial, Reason and justification, Primary
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C0422727
- UMLS CUI [1,2]
- C0566251
- UMLS CUI [1,3]
- C0205225
Descripción
Clinical study case, Investigator Signature
Tipo de datos
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])