ID
38857
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 subject's laboratory tests and should be filled out at Visit 1, 6 (liver tests only) , 8, EW, Day 7 Follow Up (unless Day 7 FU follows Early Withdrawal Visit) and Day 14 Follow Up (only if abnormal at previous Visit). Additionally, this form is used to record unscheduled (repeat) measurements.
Link
https://clinicaltrials.gov/ct2/show/NCT00992160
Keywords
Versions (2)
- 2/24/19 2/24/19 -
- 11/10/19 11/10/19 -
Copyright Holder
GlaxoSmithKline
Uploaded on
November 10, 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
Laboratory Tests
- StudyEvent: ODM
Description
Lab
Alias
- UMLS CUI-1
- C0022885
Description
If done, fill in date/time below. Not applicable to Visit 6.
Data type
text
Alias
- UMLS CUI [1,1]
- C0018941
- UMLS CUI [1,2]
- C0200345
Description
If done. Not applicable to Visit 6.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0018941
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C1264639
Description
If done and other day than haematology, fill in date/time below At Visit 6, record Clinical Chemistry/Liver Function tests only. Hence, option "Same as the Haematology sample" is not available at this visit.
Data type
text
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0200345
Description
If done and other day than haematology
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0008000
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C1264639
Description
If done, fill in date/time below. Not applicable to Visit 6.
Data type
text
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0200345
Description
If done. Not applicable to Visit 6.
Data type
datetime
Alias
- UMLS CUI [1,1]
- C0042014
- UMLS CUI [1,2]
- C0200345
- UMLS CUI [1,3]
- C1264639
Description
Electronically Transferred Lab Data
Alias
- UMLS CUI-1
- C0022885
- UMLS CUI-2
- C0205341
Similar models
Laboratory Tests
- StudyEvent: ODM
C2985720 (UMLS CUI [2])
C0200345 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0200345 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0200345 (UMLS CUI [1,2])
C0200345 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,3])
C0205341 (UMLS CUI-2)
C0332307 (UMLS CUI [1,2])
C1264639 (UMLS CUI [1,2])