ID
44091
Description
Study ID: 107979 Clinical Study ID: TXA107979 Study Title: TXA107979: A Randomized, Multicenter, Placebo-Controlled, Parallel Group Study to Evaluate the Efficacy and Safety of a Combination Product Containing Sumatriptan and Naproxen Sodium for the Acute Treatment of Migraine in Adolescents Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00843024 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 3 Study Recruitment Status: Completed Generic Name: sumatriptan/naproxen Trade Name: Treximet Study Indication: Migraine Disorders CRF Seiten: 879-993
Mots-clés
Versions (3)
- 21/06/2018 21/06/2018 -
- 21/06/2018 21/06/2018 -
- 20/09/2021 20/09/2021 -
Détendeur de droits
GlaxoSmithKline
Téléchargé le
20 septembre 2021
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY-NC 3.0
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TXA107979: Sumatriptan and Naproxen Sodium for the Acute Treatment of Migraine NCT00843024
Attack 1 Diary
- StudyEvent: ODM
Description
Migraine attack 1 symptoms
Alias
- UMLS CUI-1
- C0149931
- UMLS CUI-2
- C1457887
Description
start date migraine attack
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0149931
- UMLS CUI [1,2]
- C0808070
Description
woke up with migraine headache pain
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0442696
- UMLS CUI [1,2]
- C0149931
- UMLS CUI [1,3]
- C0018681
Description
migraine with aura
Type de données
boolean
Alias
- UMLS CUI [1]
- C0154723
Description
pain worsened by physical activity
Type de données
boolean
Alias
- UMLS CUI [1,1]
- C0018681
- UMLS CUI [1,2]
- C4054844
Description
migraine headache pain quality
Type de données
text
Alias
- UMLS CUI [1,1]
- C0149931
- UMLS CUI [1,2]
- C0018681
- UMLS CUI [1,3]
- C1148406
Description
migraine headache pain location
Type de données
text
Alias
- UMLS CUI [1,1]
- C0149931
- UMLS CUI [1,2]
- C0018681
- UMLS CUI [1,3]
- C0030193
- UMLS CUI [1,4]
- C0450429
Description
Investigational Product
Description
Start date
Type de données
date
Unités de mesure
- DDMONYYYY
Alias
- UMLS CUI [1]
- C0808070
Description
Start time
Type de données
time
Unités de mesure
- hh:mm
Alias
- UMLS CUI [1]
- C1301880
Description
Stop Date
Type de données
date
Unités de mesure
- DDMONYYYY
Alias
- UMLS CUI [1]
- C0806020
Description
Migraine attack 1 headache pain and symptoms
Alias
- UMLS CUI-1
- C0149931
- UMLS CUI-2
- C0018681
- UMLS CUI-3
- C0030193
- UMLS CUI-4
- C1457887
Description
time since drug intake
Type de données
text
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C1512806
Description
migraine headache pain with scale
Type de données
text
Alias
- UMLS CUI [1,1]
- C0149931
- UMLS CUI [1,2]
- C0018681
- UMLS CUI [1,3]
- C1504479
Description
Nausea
Type de données
boolean
Alias
- UMLS CUI [1]
- C0027497
Description
Vomiting
Type de données
integer
Alias
- UMLS CUI [1]
- C0042963
Description
Light sensitivity
Type de données
boolean
Alias
- UMLS CUI [1]
- C0085636
Description
Sound sensitivity
Type de données
boolean
Alias
- UMLS CUI [1]
- C2938899
Description
Medications taken
Alias
- UMLS CUI-1
- C2347852
Description
Sequence Number
Type de données
text
Alias
- UMLS CUI [1]
- C2348184
Description
Drug name
Type de données
text
Alias
- UMLS CUI [1]
- C0013227
Description
Modified reported term
Type de données
text
Alias
- UMLS CUI [1]
- C2826819
Description
Date and time medication taken
Type de données
datetime
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0011008
- UMLS CUI [1,3]
- C0040223
Description
Primary Reason Medication Taken
Type de données
text
Description
Specify other reason
Type de données
text
Alias
- UMLS CUI [1]
- C2826696
Description
Ability to function
Alias
- UMLS CUI-1
- C0441655
- UMLS CUI-2
- C0085732
Description
time since drug intake
Type de données
text
Alias
- UMLS CUI [1,1]
- C0011008
- UMLS CUI [1,2]
- C0304229
- UMLS CUI [1,3]
- C1512806
Description
ability to perform usual activities
Type de données
text
Alias
- UMLS CUI [1,1]
- C0441655
- UMLS CUI [1,2]
- C0085732
Description
Investigational product accountability
Alias
- UMLS CUI-1
- C0304229
- UMLS CUI-2
- C0078889
Description
investigational product container number
Type de données
integer
Alias
- UMLS CUI [1,1]
- C3898691
- UMLS CUI [1,2]
- C0449788
Description
total number of tablets dispensed
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0805077
- UMLS CUI [1,2]
- C0039225
Description
total number of tablets taken
Type de données
integer
Alias
- UMLS CUI [1,1]
- C0039225
- UMLS CUI [1,2]
- C0237753
- UMLS CUI [1,3]
- C1883727
Description
Returned Date
Type de données
date
Alias
- UMLS CUI [1,1]
- C0013227
- UMLS CUI [1,2]
- C0180098
- UMLS CUI [1,3]
- C0332156
- UMLS CUI [1,4]
- C0011008
Description
Sequence Number
Type de données
text
Alias
- UMLS CUI [1,1]
- C1519255
- UMLS CUI [1,2]
- C2348184
Description
total number of tablets returned
Type de données
integer
Alias
- UMLS CUI [1,1]
- C2699071
- UMLS CUI [1,2]
- C0039225
Description
Investigational Product
Alias
- UMLS CUI-1
- C0304229
Description
Language used in diary assessment
Alias
- UMLS CUI-1
- C3890583
- UMLS CUI-2
- C0023008
Similar models
Attack 1 Diary
- StudyEvent: ODM
C1457887 (UMLS CUI-2)
C0808070 (UMLS CUI [1,2])
C0149931 (UMLS CUI [1,2])
C0018681 (UMLS CUI [1,3])
C4054844 (UMLS CUI [1,2])
C0018681 (UMLS CUI [1,2])
C1148406 (UMLS CUI [1,3])
C0018681 (UMLS CUI [1,2])
C0030193 (UMLS CUI [1,3])
C0450429 (UMLS CUI [1,4])
C0018681 (UMLS CUI-2)
C0030193 (UMLS CUI-3)
C1457887 (UMLS CUI-4)
C0304229 (UMLS CUI [1,2])
C1512806 (UMLS CUI [1,3])
C0018681 (UMLS CUI [1,2])
C1504479 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,3])
C0304229 (UMLS CUI [1,2])
C1512806 (UMLS CUI [1,3])
C0085732 (UMLS CUI [1,2])
C0078889 (UMLS CUI-2)
C0449788 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C0237753 (UMLS CUI [1,2])
C1883727 (UMLS CUI [1,3])
C0180098 (UMLS CUI [1,2])
C0332156 (UMLS CUI [1,3])
C0011008 (UMLS CUI [1,4])
C2348184 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,2])
C0023008 (UMLS CUI-2)
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