ID
35341
Descripción
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
Palabras clave
Versiones (2)
- 1/3/19 1/3/19 -
- 10/11/19 10/11/19 -
Titular de derechos de autor
GlaxoSmithKline
Subido en
1 de marzo de 2019
DOI
Para solicitar uno, por favor iniciar sesión.
Licencia
Creative Commons BY-NC 3.0
Comentarios del modelo :
Puede comentar sobre el modelo de datos aquí. A través de las burbujas de diálogo en los grupos de elementos y elementos, puede agregar comentarios específicos.
Comentarios de grupo de elementos para :
Comentarios del elemento para :
Para descargar modelos de datos, debe haber iniciado sesión. Por favor iniciar sesión o Registrate gratis.
Polysomnographic Assessment of Vestipitant for the Treatment of Primary Insomnia NCT00992160
Study Continuation
- StudyEvent: ODM
Descripción
Study Continuation
Alias
- UMLS CUI-1
- C0805733
- UMLS CUI-2
- C0008976
Descripción
Study Continuation
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C2348568
Descripción
Screen Failure
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1710476
Descripción
Screen Failure Date
Tipo de datos
date
Alias
- UMLS CUI [1,1]
- C1710476
- UMLS CUI [1,2]
- C0011008
Descripción
Reason for Failure: Inclusion/Exclusion Criteria
Tipo de datos
boolean
Alias
- UMLS CUI [1]
- C1512693
- UMLS CUI [2]
- C0680251
- UMLS CUI [3,1]
- C0566251
- UMLS CUI [3,2]
- C1710476
Descripción
Reason for Failure: Investigator Discretion
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C1710476
- UMLS CUI [2,1]
- C0008961
- UMLS CUI [2,2]
- C0022423
Descripción
Reason for Failure:Failed PSG inclusion criteria on Central PSG judgement
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C0566251
- UMLS CUI [1,2]
- C1710476
- UMLS CUI [2,1]
- C0162701
- UMLS CUI [2,2]
- C1512693
Descripción
Reason for Failure: Failed PSG inclusion criteria on Investigator judgement
Tipo de datos
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
Descripción
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.
Tipo de datos
boolean
Alias
- UMLS CUI [1,1]
- C1706256
- UMLS CUI [1,2]
- C2346576
Descripción
lf not, click on the RETURN button below
Tipo de datos
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])