ID

36662

Description

Effectiveness of Conversion to Sirolimus Versus Calcineurin Inhibitor (CNI) Reduction in Renal Transplant Patients With Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00922129

Link

https://clinicaltrials.gov/show/NCT00922129

Keywords

Versions (3)
  1. 1/17/19 1/17/19 -
  2. 5/27/19 5/27/19 -
  3. 5/29/19 5/29/19 -
Copyright Holder

St. Joseph's Healthcare Hamilton

Uploaded on

May 29, 2019

DOI

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License

Creative Commons BY-NC 3.0
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Sirolimus in Renal Transplant Patients with Prostate Cancer NCT00922129

English

Eligibility Criteria

1 forms  
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
male patients ≤ 50 years in their post renal transplant follow-up
Description

Gender and age and in post renal transplant follow-up

Data type

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C0001779
UMLS CUI [3,1]
C0022671
UMLS CUI [3,2]
C1522577
biopsy confirmed prostate cancer
Description

biopsy confirmed prostate cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0194804
UMLS CUI [1,3]
C0750484
stable renal function with GFR ≥ 40 ml/min
Description

stable renal function (by GFR)

Data type

boolean

Alias
UMLS CUI [1,1]
C0232804
UMLS CUI [1,2]
C0205360
UMLS CUI [2]
C0017654
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with metastatic disease
Description

metastatic disease

Data type

boolean

Alias
UMLS CUI [1]
C0027627
uncontrolled hyperlipidemia
Description

uncontrolled hyperlipidemia

Data type

boolean

Alias
UMLS CUI [1,1]
C0020473
UMLS CUI [1,2]
C0205318
proteinuria > 500 mg/day
Description

proteinuria

Data type

boolean

Alias
UMLS CUI [1]
C0033687
biopsy evidence of acute rejection within the past 3 months
Description

recent biopsy evidence of acute rejection

Data type

boolean

Alias
UMLS CUI [1,1]
C0332185
UMLS CUI [1,2]
C0403588
UMLS CUI [1,3]
C0005558
existence of any surgical or medical condition, other than the current transplant, which in the opinion of the investigator might significantly alter the absorption, distribution, metabolism or excretion of study medication
Description

surgical or medical condition, other than the current transplant, which might significantly alter the absorption, distribution, metabolism or excretion of study medication

Data type

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C0392760
UMLS CUI [1,3]
C0750502
UMLS CUI [1,4]
C0237442
UMLS CUI [1,5]
C0304229
UMLS CUI [2,1]
C0543467
UMLS CUI [2,2]
C0392760
UMLS CUI [2,3]
C0750502
UMLS CUI [2,4]
C1378698
UMLS CUI [2,5]
C0304229
UMLS CUI [3,1]
C0543467
UMLS CUI [3,2]
C0392760
UMLS CUI [3,3]
C0750502
UMLS CUI [3,4]
C0025519
UMLS CUI [3,5]
C0304229
UMLS CUI [4,1]
C0543467
UMLS CUI [4,2]
C0392760
UMLS CUI [4,3]
C0750502
UMLS CUI [4,4]
C0683141
UMLS CUI [4,5]
C0304229
UMLS CUI [5,1]
C0012634
UMLS CUI [5,2]
C0392760
UMLS CUI [5,3]
C0750502
UMLS CUI [5,4]
C0237442
UMLS CUI [5,5]
C0304229
UMLS CUI [6,1]
C0012634
UMLS CUI [6,2]
C0392760
UMLS CUI [6,3]
C0750502
UMLS CUI [6,4]
C1378698
UMLS CUI [6,5]
C0304229
UMLS CUI [7,1]
C0012634
UMLS CUI [7,2]
C0392760
UMLS CUI [7,3]
C0750502
UMLS CUI [7,4]
C0025519
UMLS CUI [7,5]
C0304229
UMLS CUI [8,1]
C0012634
UMLS CUI [8,2]
C0392760
UMLS CUI [8,3]
C0750502
UMLS CUI [8,4]
C0683141
UMLS CUI [8,5]
C0304229
UMLS CUI [9,1]
C1705847
UMLS CUI [9,2]
C0521116
UMLS CUI [9,3]
C0029216
patients with mental illness
Description

mental illness

Data type

boolean

Alias
UMLS CUI [1]
C0004936
inability to cooperate or communicate with the investigator or unable to complete self administered questionnaires
Description

inability to cooperate or communicate with the investigator or unable to complete self administered questionnaires

Data type

boolean

Alias
UMLS CUI [1,1]
C1299582
UMLS CUI [1,2]
C1321605
UMLS CUI [2,1]
C0332268
UMLS CUI [2,2]
C2364293
UMLS CUI [2,3]
C0035173
UMLS CUI [3,1]
C1299582
UMLS CUI [3,2]
C0205197
UMLS CUI [3,3]
C1519231
UMLS CUI [3,4]
C0034394
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Similar models

Eligibility Criteria

1 forms
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Gender and age and in post renal transplant follow-up
Item
male patients ≤ 50 years in their post renal transplant follow-up
boolean
C0079399 (UMLS CUI [1])
C0001779 (UMLS CUI [2])
C0022671 (UMLS CUI [3,1])
C1522577 (UMLS CUI [3,2])
biopsy confirmed prostate cancer
Item
biopsy confirmed prostate cancer
boolean
C0600139 (UMLS CUI [1,1])
C0194804 (UMLS CUI [1,2])
C0750484 (UMLS CUI [1,3])
stable renal function (by GFR)
Item
stable renal function with GFR ≥ 40 ml/min
boolean
C0232804 (UMLS CUI [1,1])
C0205360 (UMLS CUI [1,2])
C0017654 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
metastatic disease
Item
patients with metastatic disease
boolean
C0027627 (UMLS CUI [1])
uncontrolled hyperlipidemia
Item
uncontrolled hyperlipidemia
boolean
C0020473 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
proteinuria
Item
proteinuria > 500 mg/day
boolean
C0033687 (UMLS CUI [1])
recent biopsy evidence of acute rejection
Item
biopsy evidence of acute rejection within the past 3 months
boolean
C0332185 (UMLS CUI [1,1])
C0403588 (UMLS CUI [1,2])
C0005558 (UMLS CUI [1,3])
surgical or medical condition, other than the current transplant, which might significantly alter the absorption, distribution, metabolism or excretion of study medication
Item
existence of any surgical or medical condition, other than the current transplant, which in the opinion of the investigator might significantly alter the absorption, distribution, metabolism or excretion of study medication
boolean
C0543467 (UMLS CUI [1,1])
C0392760 (UMLS CUI [1,2])
C0750502 (UMLS CUI [1,3])
C0237442 (UMLS CUI [1,4])
C0304229 (UMLS CUI [1,5])
C0543467 (UMLS CUI [2,1])
C0392760 (UMLS CUI [2,2])
C0750502 (UMLS CUI [2,3])
C1378698 (UMLS CUI [2,4])
C0304229 (UMLS CUI [2,5])
C0543467 (UMLS CUI [3,1])
C0392760 (UMLS CUI [3,2])
C0750502 (UMLS CUI [3,3])
C0025519 (UMLS CUI [3,4])
C0304229 (UMLS CUI [3,5])
C0543467 (UMLS CUI [4,1])
C0392760 (UMLS CUI [4,2])
C0750502 (UMLS CUI [4,3])
C0683141 (UMLS CUI [4,4])
C0304229 (UMLS CUI [4,5])
C0012634 (UMLS CUI [5,1])
C0392760 (UMLS CUI [5,2])
C0750502 (UMLS CUI [5,3])
C0237442 (UMLS CUI [5,4])
C0304229 (UMLS CUI [5,5])
C0012634 (UMLS CUI [6,1])
C0392760 (UMLS CUI [6,2])
C0750502 (UMLS CUI [6,3])
C1378698 (UMLS CUI [6,4])
C0304229 (UMLS CUI [6,5])
C0012634 (UMLS CUI [7,1])
C0392760 (UMLS CUI [7,2])
C0750502 (UMLS CUI [7,3])
C0025519 (UMLS CUI [7,4])
C0304229 (UMLS CUI [7,5])
C0012634 (UMLS CUI [8,1])
C0392760 (UMLS CUI [8,2])
C0750502 (UMLS CUI [8,3])
C0683141 (UMLS CUI [8,4])
C0304229 (UMLS CUI [8,5])
C1705847 (UMLS CUI [9,1])
C0521116 (UMLS CUI [9,2])
C0029216 (UMLS CUI [9,3])
mental illness
Item
patients with mental illness
boolean
C0004936 (UMLS CUI [1])
inability to cooperate or communicate with the investigator or unable to complete self administered questionnaires
Item
inability to cooperate or communicate with the investigator or unable to complete self administered questionnaires
boolean
C1299582 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0332268 (UMLS CUI [2,1])
C2364293 (UMLS CUI [2,2])
C0035173 (UMLS CUI [2,3])
C1299582 (UMLS CUI [3,1])
C0205197 (UMLS CUI [3,2])
C1519231 (UMLS CUI [3,3])
C0034394 (UMLS CUI [3,4])
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