ID
35197
Beschrijving
Study ID: 111364 Clinical Study ID: 111364 Study Title: A 28-Day, Polysomnographic and subjective assessment of Vestipitant (15mg/day) for the treatment of Primary Insomnia in adult Outpatients Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00992160 Clinicaltrials.gov Links: https://clinicaltrials.gov/ct2/show/NCT00992160 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 2 Study Recruitment Status: Completed Generic Name: Vestipitant, Placebo Trade Name: N/A Study Indication: Primary Insomnia, Sleep Disorders The purpouse of this form is to record the results of the subjects ECG and should be filled out at Visit 1, 6, 7, EW, Day 7 Follow Up and Day 14 Follow Up.
Link
https://clinicaltrials.gov/ct2/show/NCT00992160
Trefwoorden
Versies (3)
- 24-02-19 24-02-19 -
- 01-03-19 01-03-19 -
- 10-11-19 10-11-19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
24 februari 2019
DOI
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Licentie
Creative Commons BY-NC 3.0
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Polysomnographic Assessment of Vestipitant for the Treatment of Primary Insomnia NCT00992160
12-Lead-ECG
- StudyEvent: ODM
Beschrijving
12-Lead-ECG
Alias
- UMLS CUI-1
- C0430456
Beschrijving
This item applies for all visit except visit 1
Datatype
date
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0011008
Beschrijving
This item applies for all visit except visit 1
Datatype
time
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0040223
Beschrijving
Date of ECG
Datatype
date
Alias
- UMLS CUI [1]
- C2826640
Beschrijving
Time of ECG
Datatype
time
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C1301880
Beschrijving
Result of the ECG
Datatype
text
Alias
- UMLS CUI [1]
- C0438154
Similar models
12-Lead-ECG
- StudyEvent: ODM
C2985720 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0040223 (UMLS CUI [1,2])
C1301880 (UMLS CUI [1,2])