ID

42013

Beschrijving

This is an open-label (all people know the identity of the intervention), multicenter study in genotype 1 chronic HCV infected liver transplant patients who will be treated for 12 weeks with telaprevir 750 mg every 8 hours given in combination with Peg-IFN-alfa-2a and ribavirin followed by 36 weeks of treatment with Peg-IFN-alfa-2a and ribavirin alone. The total treatment duration will be 48 weeks. Safety will be evaluated throughout the study and will include evaluations of adverse events, clinical laboratory tests, electrocardiogram, vital signs, and physical examination. NCT01571583

Trefwoorden

  1. 21-03-16 21-03-16 -
  2. 15-03-21 15-03-21 - Dr. rer. medic Philipp Neuhaus
Houder van rechten

CC BY-NC 3.0

Geüploaded op

15 maart 2021

DOI

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Licentie

Creative Commons BY-NC 3.0

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VX-950HPC3006 NCT01571583 Administration of TAC/CsA

VX-950HPC3006 NCT01571583 Administration of TAC/CsA

Administration of TAC/CsA
Beschrijving

Administration of TAC/CsA

therapy
Beschrijving

therapy

Datatype

integer

Alias
UMLS CUI [1]
C0087111
UMLS CUI [2]
C0085149
UMLS CUI [3]
C0010592
Dose per intake
Beschrijving

Dose per intake

Datatype

text

Alias
UMLS CUI [1]
C3174092
unit
Beschrijving

Unit

Datatype

integer

Alias
UMLS CUI [1]
C1519795
frequency
Beschrijving

frequency

Datatype

text

Alias
UMLS CUI [1]
C3476109
route of administration
Beschrijving

route of administration

Datatype

integer

Alias
UMLS CUI [1]
C0013153
start of therapy
Beschrijving

start of therapy

Datatype

date

Alias
UMLS CUI [1]
C3173309
end of therapy
Beschrijving

please complete "ongoing" only at the end of the trial

Datatype

integer

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C0444930
reason for change
Beschrijving

reason for change

Datatype

integer

Alias
UMLS CUI [1,1]
C1299575
UMLS CUI [1,2]
C1272707
row number
Beschrijving

row number

Datatype

text

Alias
UMLS CUI [1]
C0237753

Similar models

VX-950HPC3006 NCT01571583 Administration of TAC/CsA

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Administration of TAC/CsA
Item
therapy
integer
C0087111 (UMLS CUI [1])
C0085149 (UMLS CUI [2])
C0010592 (UMLS CUI [3])
Code List
therapy
CL Item
Tacrolimus (1)
CL Item
Cyclosporin A (2)
Dose per intake
Item
Dose per intake
text
C3174092 (UMLS CUI [1])
Item
unit
integer
C1519795 (UMLS CUI [1])
Code List
unit
CL Item
mg (1)
CL Item
other please specify (2)
frequency
Item
frequency
text
C3476109 (UMLS CUI [1])
Item
route of administration
integer
C0013153 (UMLS CUI [1])
Code List
route of administration
CL Item
oral (1)
CL Item
other specify (2)
start of therapy
Item
start of therapy
date
C3173309 (UMLS CUI [1])
Item
end of therapy
integer
C0087111 (UMLS CUI [1,1])
C0444930 (UMLS CUI [1,2])
Code List
end of therapy
CL Item
end date please specify (1)
CL Item
ongoing at end of the trial (2)
Item
reason for change
integer
C1299575 (UMLS CUI [1,1])
C1272707 (UMLS CUI [1,2])
Code List
reason for change
CL Item
PK (1)
CL Item
AE (2)
CL Item
Other please specify (3)
row number
Item
row number
text
C0237753 (UMLS CUI [1])

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