ID

16785

Description

QUTENZA™ versus Pregabalin in Subjects with Peripheral Neuropathic Pain: an Open-label, Randomized, Multicenter, Non-inferiority Efficacy and Tolerability Study Medicine or Vaccine (generic name) capsaicin Visit: Week 2 - 4 Telephone Contact in Week 6 Sponsor Identification Number QTZ-EC-0004 Trial Registry Identification Number(#'s) NCT01713426 EudraCT Number: 2011-005872-41

Mots-clés

  1. 07/08/2016 07/08/2016 -
Téléchargé le

7 août 2016

DOI

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Licence

Creative Commons BY-NC-ND 3.0

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Visit and Telephone Contact QTZ-EC-0004 ELEVATE NCT01713426

Visit and Telephone Contact QTZ-EC-0004 ELEVATE NCT01713426

Date of Visit
Description

Date of Visit

Alias
UMLS CUI-1
C1320303
Was the visit performed? If No, then all other forms with the Form Not Done field in this visit will be marked not done. If Yes, please provide the Date of Visit:
Description

Visit

Type de données

boolean

Alias
UMLS CUI [1]
C0545082
If Yes, please provide the Date of Visit.
Description

Date of visit

Type de données

date

Unités de mesure
  • dd/MMM/yyyy
dd/MMM/yyyy
Healthcare Resource Use
Description

Healthcare Resource Use

Alias
UMLS CUI-1
C1704738
Form Not Done (Form Not Done should only be marked for subjects that are `RANDOMIZED/REGISTERED BUT NEVER RECEIVED/DISPENSED STUDY DRUG`.)
Description

Healthcare Resource Use

Type de données

text

Alias
UMLS CUI [1]
C1704738
Number of contacts with a healthcare professional related to neuropathic pain, since the last visit.
Description

Number of contacts for Neuropathic Pains

Type de données

float

Alias
UMLS CUI [1,1]
C1444281
UMLS CUI [1,2]
C0449788
UMLS CUI [1,3]
C3714625
Number of contacts with a healthcare professional for other causes, since the last visit
Description

Number of contacts: Specification

Type de données

float

Alias
UMLS CUI [1,1]
C1444281
UMLS CUI [1,2]
C0449788
UMLS CUI [1,3]
C2348235
Tolerability Assessment
Description

Tolerability Assessment

Alias
UMLS CUI-1
C3274448
Form Not Done (Form Not Done should only be marked for subjects that are `RANDOMIZED/ REGISTERED BUT NEVER RECEIVED/ DISPENSED STUDY DRUG`).
Description

Tolerability Assessment

Type de données

text

Alias
UMLS CUI [1]
C3274448
Has diary been reviewed, and any existing Adverse Events recorded in the eCRF?
Description

Adverse Event

Type de données

boolean

Alias
UMLS CUI [1]
C0877248
Telephone Contact: Date
Description

Telephone Contact: Date

Alias
UMLS CUI-1
C0420309
UMLS CUI-2
C0011008
Was this visit performed? (If No, then all other forms with the Form Not Done field in this visit will be marked not done.
Description

Telephone Contact

Type de données

boolean

Alias
UMLS CUI [1]
C0420309
If Yes, please provide the Date of Visit
Description

Telephone Contact: Date

Type de données

date

Alias
UMLS CUI [1,1]
C0420309
UMLS CUI [1,2]
C0011008
Telephone Contact: Tolerability Assessment
Description

Telephone Contact: Tolerability Assessment

Alias
UMLS CUI-1
C0420309
UMLS CUI-2
C3274448
Form Not Done (Form Not Done should only be marekd for subjects that are "RANDOMIZED/ REGISTERED BUT NEVER RECEIVED/DISPRENSED STUDY DRUG").
Description

Telephone Contact: Tolerability Assessment

Type de données

text

Alias
UMLS CUI [1,1]
C0420309
UMLS CUI [1,2]
C3274448
Has diary been reviewed, and any existing Adverse Events recorded in the eCRF?
Description

Telephone Contact: Adverse Event

Type de données

boolean

Alias
UMLS CUI [1,1]
C0420309
UMLS CUI [1,2]
C0877248

Similar models

Visit and Telephone Contact QTZ-EC-0004 ELEVATE NCT01713426

Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Date of Visit
C1320303 (UMLS CUI-1)
Visit
Item
Was the visit performed? If No, then all other forms with the Form Not Done field in this visit will be marked not done. If Yes, please provide the Date of Visit:
boolean
C0545082 (UMLS CUI [1])
Date of visit
Item
If Yes, please provide the Date of Visit.
date
Item Group
Healthcare Resource Use
C1704738 (UMLS CUI-1)
Item
Form Not Done (Form Not Done should only be marked for subjects that are `RANDOMIZED/REGISTERED BUT NEVER RECEIVED/DISPENSED STUDY DRUG`.)
text
C1704738 (UMLS CUI [1])
Code List
Form Not Done (Form Not Done should only be marked for subjects that are `RANDOMIZED/REGISTERED BUT NEVER RECEIVED/DISPENSED STUDY DRUG`.)
CL Item
Done (Done)
CL Item
Not Done (Not Done)
Number of contacts for Neuropathic Pains
Item
Number of contacts with a healthcare professional related to neuropathic pain, since the last visit.
float
C1444281 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
C3714625 (UMLS CUI [1,3])
Number of contacts: Specification
Item
Number of contacts with a healthcare professional for other causes, since the last visit
float
C1444281 (UMLS CUI [1,1])
C0449788 (UMLS CUI [1,2])
C2348235 (UMLS CUI [1,3])
Item Group
Tolerability Assessment
C3274448 (UMLS CUI-1)
Item
Form Not Done (Form Not Done should only be marked for subjects that are `RANDOMIZED/ REGISTERED BUT NEVER RECEIVED/ DISPENSED STUDY DRUG`).
text
C3274448 (UMLS CUI [1])
Code List
Form Not Done (Form Not Done should only be marked for subjects that are `RANDOMIZED/ REGISTERED BUT NEVER RECEIVED/ DISPENSED STUDY DRUG`).
CL Item
Done (Done)
CL Item
Not Done (Not Done)
Adverse Event
Item
Has diary been reviewed, and any existing Adverse Events recorded in the eCRF?
boolean
C0877248 (UMLS CUI [1])
Item Group
Telephone Contact: Date
C0420309 (UMLS CUI-1)
C0011008 (UMLS CUI-2)
Telephone Contact
Item
Was this visit performed? (If No, then all other forms with the Form Not Done field in this visit will be marked not done.
boolean
C0420309 (UMLS CUI [1])
Telephone Contact: Date
Item
If Yes, please provide the Date of Visit
date
C0420309 (UMLS CUI [1,1])
C0011008 (UMLS CUI [1,2])
Item Group
Telephone Contact: Tolerability Assessment
C0420309 (UMLS CUI-1)
C3274448 (UMLS CUI-2)
Item
Form Not Done (Form Not Done should only be marekd for subjects that are "RANDOMIZED/ REGISTERED BUT NEVER RECEIVED/DISPRENSED STUDY DRUG").
text
C0420309 (UMLS CUI [1,1])
C3274448 (UMLS CUI [1,2])
Code List
Form Not Done (Form Not Done should only be marekd for subjects that are "RANDOMIZED/ REGISTERED BUT NEVER RECEIVED/DISPRENSED STUDY DRUG").
CL Item
Done (Done)
CL Item
Not Done (Not Done)
Telephone Contact: Adverse Event
Item
Has diary been reviewed, and any existing Adverse Events recorded in the eCRF?
boolean
C0420309 (UMLS CUI [1,1])
C0877248 (UMLS CUI [1,2])

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