ID
35341
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 purpose of this form is to check if the subject will return for the next visit and should be filled out at visit 1.
Link
https://clinicaltrials.gov/ct2/show/NCT00992160
Trefwoorden
Versies (2)
- 01/03/19 01/03/19 -
- 10/11/19 10/11/19 -
Houder van rechten
GlaxoSmithKline
Geüploaded op
1 marzo 2019
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY-NC 3.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Polysomnographic Assessment of Vestipitant for the Treatment of Primary Insomnia NCT00992160
Study Continuation
- StudyEvent: ODM
Beschrijving
Study Continuation
Alias
- UMLS CUI-1
- C0805733
- UMLS CUI-2
- C0008976
Beschrijving
Study Continuation
Datatype
boolean
Alias
- UMLS CUI [1]
- C2348568
Beschrijving
Screen Failure
Datatype
boolean
Alias
- UMLS CUI [1]
- C1710476
Beschrijving
Screen Failure Date
Datatype
date
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0011008
Beschrijving
Reason for Failure: Inclusion/Exclusion Criteria
Datatype
boolean
Alias
- UMLS CUI [1]
- C1512693
- UMLS CUI [2]
- C0680251
- UMLS CUI [3,1]
- C0566251
- UMLS CUI [3,2]
- C1710476
Beschrijving
Reason for Failure: Investigator Discretion
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C1710476
- UMLS CUI [2,1]
- C0008961
- UMLS CUI [2,2]
- C0022423
Beschrijving
Reason for Failure:Failed PSG inclusion criteria on Central PSG judgement
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C1710476
- UMLS CUI [2,1]
- C0162701
- UMLS CUI [2,2]
- C1512693
Beschrijving
Reason for Failure: Failed PSG inclusion criteria on Investigator judgement
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C1710476
- UMLS CUI [2,1]
- C0162701
- UMLS CUI [2,2]
- C1512693
- UMLS CUI [3,1]
- C0008961
- UMLS CUI [3,2]
- C0022423
Beschrijving
By ticking or unticking this box you are evoking a change to this form that will invalidate the original signature and will revert the form back to an unsigned state. This should be done when significant changes (e.g. those that require medical opinion or other significant situations) occur after the original signature. If the box is already ticked upon arrival on this form, unticking and submitting it accomplishes the same task as licking and submitting if; that is, the signature will be invalidated in both instances.
Datatype
boolean
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C2346576
Beschrijving
lf not, click on the RETURN button below
Datatype
text
Alias
- UMLS CUI [1]
- C2346576
Similar models
Study Continuation
- StudyEvent: ODM
C2985720 (UMLS CUI [1,2])
C0011008 (UMLS CUI [1,2])
C0680251 (UMLS CUI [2])
C0566251 (UMLS CUI [3,1])
C1710476 (UMLS CUI [3,2])
C1710476 (UMLS CUI [1,2])
C0008961 (UMLS CUI [2,1])
C0022423 (UMLS CUI [2,2])
C1710476 (UMLS CUI [1,2])
C0162701 (UMLS CUI [2,1])
C1512693 (UMLS CUI [2,2])
C1710476 (UMLS CUI [1,2])
C0162701 (UMLS CUI [2,1])
C1512693 (UMLS CUI [2,2])
C0008961 (UMLS CUI [3,1])
C0022423 (UMLS CUI [3,2])
C2346576 (UMLS CUI [1,2])