ID

17494

Description

An open label, dose titration study of sevelamer carbonate tablets dosed three times a day in hyperphosphatemic chronic kidney disease patients not on dialysis Name of Sponsor: Genzyme Europe BV Country: Netherlands https://www.clinicaltrialsregister.eu/ctr-search/trial/2005-003233-41/DE#A

Link

https://www.clinicaltrialsregister.eu/ctr-search/trial/2005-003233-41/DE#A

Keywords

  1. 9/18/16 9/18/16 -
Uploaded on

September 18, 2016

DOI

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License

Creative Commons BY-NC 3.0

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Concomitant Medications Genzyme Chronic Kidney Disease EudraCT 2005-003233-41

Concomitant Medications Genzyme Chronic Kidney Disease EudraCT 2005-003233-41

Patient administration
Description

Patient administration

Patient Initials
Description

Patient Initials

Data type

text

Alias
UMLS CUI [1]
C2986440
Patient ID Number
Description

Patient ID Number

Data type

integer

Alias
UMLS CUI [1]
C2348585
Concomitant Medications
Description

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Medication
Description

Medication

Data type

text

Alias
UMLS CUI [1]
C0013227
Medication Dose
Description

Medication Dose

Data type

float

Alias
UMLS CUI [1]
C3174092
Unit
Description

Medication Dose Unit

Data type

text

Alias
UMLS CUI [1]
C1519795
Route
Description

Medication Route

Data type

integer

Alias
UMLS CUI [1]
C0013153
Medication Regimen
Description

Medication Regimen

Data type

text

Alias
UMLS CUI [1]
C0237125
Start date
Description

Medication Start date

Data type

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Description

Medication Stop Date

Data type

date

Alias
UMLS CUI [1]
C2598418
Indication
Description

Medication Indication

Data type

text

Alias
UMLS CUI [1]
C3146298

Similar models

Concomitant Medications Genzyme Chronic Kidney Disease EudraCT 2005-003233-41

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Patient administration
Patient Initials
Item
Patient Initials
text
C2986440 (UMLS CUI [1])
Patient ID Number
Item
Patient ID Number
integer
C2348585 (UMLS CUI [1])
Item Group
Concomitant Medications
C2347852 (UMLS CUI-1)
Medication
Item
Medication
text
C0013227 (UMLS CUI [1])
Medication Dose
Item
Medication Dose
float
C3174092 (UMLS CUI [1])
Medication Dose Unit
Item
Unit
text
C1519795 (UMLS CUI [1])
Item
Route
integer
C0013153 (UMLS CUI [1])
Code List
Route
CL Item
Epidural (1)
CL Item
Intramuscular (2)
CL Item
Intravenous (3)
CL Item
Oral (4)
CL Item
Vaginal (5)
CL Item
Intradermal (6)
CL Item
Inhalant (7)
CL Item
Nasogastric (8)
CL Item
Rectal (9)
CL Item
Sublingual (10)
CL Item
Other (11)
Medication Regimen
Item
Medication Regimen
text
C0237125 (UMLS CUI [1])
Medication Start date
Item
Start date
date
C0808070 (UMLS CUI [1])
Medication Stop Date
Item
Stop Date
date
C2598418 (UMLS CUI [1])
Medication Indication
Item
Indication
text
C3146298 (UMLS CUI [1])

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