ID
38541
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 (3)
- 22-09-19 22-09-19 -
- 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
Non-Serious Adverse Event
- StudyEvent: ODM
Beschrijving
Non-Serious Adverse Event
Alias
- UMLS CUI-1
- C1518404
Beschrijving
Non-serious Adverse Event, Sequence Number
Datatype
integer
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2348184
Beschrijving
Non-serious Adverse Event
Datatype
text
Alias
- UMLS CUI [1]
- C1518404
Beschrijving
Non-serious Adverse Event, Adverse Event Modified Reported Term
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2826798
Beschrijving
Non-serious Adverse Event, Medical Dictionary for Regulatory Activities Terminology (MedDRA)
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1140263
Beschrijving
Non-serious Adverse Event, MedDRA Low Level Term Code
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C3898442
Beschrijving
Non-serious Adverse Event, Code, Failed
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0805701
- UMLS CUI [1,3]
- C0231175
Beschrijving
Non-serious Adverse Event, Start Date, Start time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0808070
- UMLS CUI [1,3]
- C1301880
Beschrijving
Non-serious Adverse Event, Adverse Event Outcome
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1705586
Beschrijving
Non-serious Adverse Event, End Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0806020
Beschrijving
Non-serious Adverse Event, Frequencies
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439603
Beschrijving
Non-serious Adverse Event, Severity of Adverse Event
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1710066
Beschrijving
Non-serious Adverse Event, Symptom intensity, Date of onset
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0518690
- UMLS CUI [1,3]
- C0574845
Beschrijving
Non-serious Adverse Event, Grade, Maximum
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0806909
Beschrijving
Non-serious Adverse Event, Grade, Date of onset
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0574845
Beschrijving
Non-serious Adverse Event, Grade, Symptom intensity, Maximum
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0518690
- UMLS CUI [1,4]
- C0806909
Beschrijving
Non-serious Adverse Event, Grade, Symptom intensity, Date of onset
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0441800
- UMLS CUI [1,3]
- C0518690
- UMLS CUI [1,4]
- C0574845
Beschrijving
Non-serious Adverse Event, Action Taken with Study Treatment
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C1704758
Beschrijving
Non-serious Adverse Event, Withdraw
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2349954
Beschrijving
Non-serious Adverse Event, Relationships, Experimental drug
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0439849
- UMLS CUI [1,3]
- C0304229
Beschrijving
Non-serious Adverse Event, Duration
Datatype
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C2926735
Beschrijving
Non-serious Adverse Event, Time Last Dose
Datatype
time
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0946444
Beschrijving
Intensity Changes
Alias
- UMLS CUI-1
- C1519255
- UMLS CUI-2
- C0518690
- UMLS CUI-3
- C0392747
Beschrijving
Non-serious Adverse Event, Part, Start Date, Start time
Datatype
datetime
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0808070
- UMLS CUI [1,4]
- C1301880
Beschrijving
Non-serious Adverse Event, Part, Symptom intensity
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0518690
Beschrijving
Non-serious Adverse Event, Part, Grade
Datatype
text
Alias
- UMLS CUI [1,1]
- C1518404
- UMLS CUI [1,2]
- C0449719
- UMLS CUI [1,3]
- C0441800
Beschrijving
Non-serious Adverse Event, Part, Symptom intensity, Grade
Datatype
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])