ID

17494

Beschrijving

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

Trefwoorden

  1. 18-09-16 18-09-16 -
Geüploaded op

18 september 2016

DOI

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Licentie

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
Beschrijving

Patient administration

Patient Initials
Beschrijving

Patient Initials

Datatype

text

Alias
UMLS CUI [1]
C2986440
Patient ID Number
Beschrijving

Patient ID Number

Datatype

integer

Alias
UMLS CUI [1]
C2348585
Concomitant Medications
Beschrijving

Concomitant Medications

Alias
UMLS CUI-1
C2347852
Medication
Beschrijving

Medication

Datatype

text

Alias
UMLS CUI [1]
C0013227
Medication Dose
Beschrijving

Medication Dose

Datatype

float

Alias
UMLS CUI [1]
C3174092
Unit
Beschrijving

Medication Dose Unit

Datatype

text

Alias
UMLS CUI [1]
C1519795
Route
Beschrijving

Medication Route

Datatype

integer

Alias
UMLS CUI [1]
C0013153
Medication Regimen
Beschrijving

Medication Regimen

Datatype

text

Alias
UMLS CUI [1]
C0237125
Start date
Beschrijving

Medication Start date

Datatype

date

Alias
UMLS CUI [1]
C0808070
Stop Date
Beschrijving

Medication Stop Date

Datatype

date

Alias
UMLS CUI [1]
C2598418
Indication
Beschrijving

Medication Indication

Datatype

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)
Datatype
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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