ID
38541
Beskrivning
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
Nyckelord
Versioner (3)
- 2019-09-22 2019-09-22 -
- 2019-10-24 2019-10-24 -
- 2019-10-24 2019-10-24 -
Rättsinnehavare
GlaxoSmithKline
Uppladdad den
24 oktober 2019
DOI
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Licens
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
Beskrivning
Non-Serious Adverse Event
Alias
- UMLS CUI-1
- C1518404
Beskrivning
Non-serious Adverse Event, Sequence Number
Datatyp
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2348184
Beskrivning
Non-serious Adverse Event
Datatyp
text
Alias
- UMLS CUI [1]
- C1518404
Beskrivning
Non-serious Adverse Event, Adverse Event Modified Reported Term
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2826798
Beskrivning
Non-serious Adverse Event, Medical Dictionary for Regulatory Activities Terminology (MedDRA)
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1140263
Beskrivning
Non-serious Adverse Event, MedDRA Low Level Term Code
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C3898442
Beskrivning
Non-serious Adverse Event, Code, Failed
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Beskrivning
Non-serious Adverse Event, Start Date, Start time
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Beskrivning
Non-serious Adverse Event, Adverse Event Outcome
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Beskrivning
Non-serious Adverse Event, End Date
Datatyp
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Beskrivning
Non-serious Adverse Event, Frequencies
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Beskrivning
Non-serious Adverse Event, Severity of Adverse Event
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710066
Beskrivning
Non-serious Adverse Event, Symptom intensity, Date of onset
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0574845
Beskrivning
Non-serious Adverse Event, Grade, Maximum
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Beskrivning
Non-serious Adverse Event, Grade, Date of onset
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0574845
Beskrivning
Non-serious Adverse Event, Grade, Symptom intensity, Maximum
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0518690
- UMLS CUI [1,4]
- C0806909
Beskrivning
Non-serious Adverse Event, Grade, Symptom intensity, Date of onset
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0518690
- UMLS CUI [1,4]
- C0574845
Beskrivning
Non-serious Adverse Event, Action Taken with Study Treatment
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1704758
Beskrivning
Non-serious Adverse Event, Withdraw
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2349954
Beskrivning
Non-serious Adverse Event, Relationships, Experimental drug
Datatyp
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0304229
Beskrivning
Non-serious Adverse Event, Duration
Datatyp
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2926735
Beskrivning
Non-serious Adverse Event, Time Last Dose
Datatyp
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0946444
Beskrivning
Intensity Changes
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C0392747
Beskrivning
Non-serious Adverse Event, Part, Start Date, Start time
Datatyp
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0808070
- UMLS CUI [1,4]
- C1301880
Beskrivning
Non-serious Adverse Event, Part, Symptom intensity
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0518690
Beskrivning
Non-serious Adverse Event, Part, Grade
Datatyp
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0441800
Beskrivning
Non-serious Adverse Event, Part, Symptom intensity, Grade
Datatyp
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])