ID
35348
Description
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 purpose 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 (10h) Follow Up and Day 14 Follow Up and can be repeatet in "logs/repeats".
Link
https://clinicaltrials.gov/ct2/show/NCT00992160
Keywords
Versions (3)
- 2/24/19 2/24/19 -
- 3/1/19 3/1/19 -
- 11/10/19 11/10/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
March 1, 2019
DOI
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License
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
Description
12-Lead-ECG
Alias
- UMLS CUI-1
- C0430456
Description
This item applies for visits 6 and 7
Data type
date
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0011008
Description
This item applies for visits 6 and 7
Data type
time
Alias
- UMLS CUI [1,1]
- C0178602
- UMLS CUI [1,2]
- C0040223
Description
Date of ECG
Data type
date
Alias
- UMLS CUI [1]
- C2826640
Description
Time of ECG
Data type
time
Alias
- UMLS CUI [1,1]
- C0430456
- UMLS CUI [1,2]
- C1301880
Description
Result of the ECG
Data type
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])