ID
38541
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 (3)
- 22/9/19 22/9/19 -
- 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
Non-Serious Adverse Event
- StudyEvent: ODM
Descripción
Non-Serious Adverse Event
Alias
- UMLS CUI-1
- C1518404
Descripción
Non-serious Adverse Event, Sequence Number
Tipo de datos
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2348184
Descripción
Non-serious Adverse Event
Tipo de datos
text
Alias
- UMLS CUI [1]
- C1518404
Descripción
Non-serious Adverse Event, Adverse Event Modified Reported Term
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2826798
Descripción
Non-serious Adverse Event, Medical Dictionary for Regulatory Activities Terminology (MedDRA)
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1140263
Descripción
Non-serious Adverse Event, MedDRA Low Level Term Code
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C3898442
Descripción
Non-serious Adverse Event, Code, Failed
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Descripción
Non-serious Adverse Event, Start Date, Start time
Tipo de datos
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Descripción
Non-serious Adverse Event, Adverse Event Outcome
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Descripción
Non-serious Adverse Event, End Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Descripción
Non-serious Adverse Event, Frequencies
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Descripción
Non-serious Adverse Event, Severity of Adverse Event
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710066
Descripción
Non-serious Adverse Event, Symptom intensity, Date of onset
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0574845
Descripción
Non-serious Adverse Event, Grade, Maximum
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Descripción
Non-serious Adverse Event, Grade, Date of onset
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0574845
Descripción
Non-serious Adverse Event, Grade, Symptom intensity, Maximum
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0518690
- UMLS CUI [1,4]
- C0806909
Descripción
Non-serious Adverse Event, Grade, Symptom intensity, Date of onset
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0518690
- UMLS CUI [1,4]
- C0574845
Descripción
Non-serious Adverse Event, Action Taken with Study Treatment
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1704758
Descripción
Non-serious Adverse Event, Withdraw
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2349954
Descripción
Non-serious Adverse Event, Relationships, Experimental drug
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0304229
Descripción
Non-serious Adverse Event, Duration
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2926735
Descripción
Non-serious Adverse Event, Time Last Dose
Tipo de datos
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0946444
Descripción
Intensity Changes
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C0392747
Descripción
Non-serious Adverse Event, Part, Start Date, Start time
Tipo de datos
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0808070
- UMLS CUI [1,4]
- C1301880
Descripción
Non-serious Adverse Event, Part, Symptom intensity
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0518690
Descripción
Non-serious Adverse Event, Part, Grade
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0441800
Descripción
Non-serious Adverse Event, Part, Symptom intensity, Grade
Tipo de datos
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0518690
- UMLS CUI [1,4]
- C0441800
Similar models
Non-Serious Adverse Event
- StudyEvent: ODM
C1300638 (UMLS CUI [1,2])
C2348184 (UMLS CUI [1,2])
C2826798 (UMLS CUI [1,2])
C1140263 (UMLS CUI [1,2])
C3898442 (UMLS CUI [1,2])
C0805701 (UMLS CUI [1,2])
C0231175 (UMLS CUI [1,3])
C0808070 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,3])
C1705586 (UMLS CUI [1,2])
C0806020 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,2])
C1710066 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,2])
C0574845 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0806909 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0574845 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,3])
C0806909 (UMLS CUI [1,4])
C0441800 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,3])
C0574845 (UMLS CUI [1,4])
C1704758 (UMLS CUI [1,2])
C2349954 (UMLS CUI [1,2])
C0439849 (UMLS CUI [1,2])
C0304229 (UMLS CUI [1,3])
C2926735 (UMLS CUI [1,2])
C0946444 (UMLS CUI [1,2])
C0518690 (UMLS CUI-2)
C0392747 (UMLS CUI-3)
C0449719 (UMLS CUI [1,2])
C0808070 (UMLS CUI [1,3])
C1301880 (UMLS CUI [1,4])
C0449719 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,3])
C0449719 (UMLS CUI [1,2])
C0441800 (UMLS CUI [1,3])
C0449719 (UMLS CUI [1,2])
C0518690 (UMLS CUI [1,3])
C0441800 (UMLS CUI [1,4])