ID

17182

Descripción

A Phase II Trial of Calcitriol and Naproxen in Patients With Recurrent Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT00383487

Link

https://clinicaltrials.gov/show/NCT00383487

Palabras clave

  1. 30/8/16 30/8/16 -
Subido en

30 de agosto de 2016

DOI

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Licencia

Creative Commons BY 4.0

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Eligibility Prostatic Neoplasms NCT00383487

Eligibility Prostatic Neoplasms NCT00383487

Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
must give written informed consent
Descripción

informed consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
histologically confirmed adenocarcinoma of the prostate
Descripción

adenocarcinoma of the prostate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007112
biochemical relapse after primary radiation therapy or surgery
Descripción

biochemical relapse

Tipo de datos

boolean

Alias
UMLS CUI [1]
C2985506
normal testosterone levels
Descripción

testosterone level

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0523912
3 rising psa after nadir, with interval between psa determinations > 2 weeks
Descripción

rising psa

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201544
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
local recurrence by ct scan
Descripción

local recurrence

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027643
distant metastases by bone scan
Descripción

distant metastasis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1269798
hypercalcemia
Descripción

hypercalcemia

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0020437
nephrolithiasis
Descripción

nephrolithiasis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0392525
renal insufficiency (serum creatinine > 1.8 mg/dl)
Descripción

serum creatinine

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201976
pancreatitis
Descripción

pancreatitis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0030305
history of ulcer or gastrointestinal bleeding
Descripción

ulcer or gastrointestinal bleeding

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0030920
UMLS CUI [2]
C0017181
more than 6 months of hormone ablation therapy
Descripción

hormone ablation therapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279492
concurrent therapy for prostate cancer
Descripción

concurrent therapy for prostate cancer

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0009429
UMLS CUI [1,2]
C0600139
uncontrolled htn
Descripción

uncontrolled hypertension

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1868885
h/o mi, cva, tia
Descripción

Myocardial Infarction, Cerebrovascular accident, Transient Ischemic Attack

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
UMLS CUI [3]
C0007787
known coronary disease/cerebrovascular disease
Descripción

coronary disease/cerebrovascular disease

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0010068
UMLS CUI [2]
C0007820
platelet counts <50
Descripción

platelet count

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0032181
patients on anticoagulants
Descripción

anticoagulants

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003280
patients on lithium
Descripción

Lithium

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0023870

Similar models

Eligibility Prostatic Neoplasms NCT00383487

Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
informed consent
Item
must give written informed consent
boolean
C0021430 (UMLS CUI [1])
adenocarcinoma of the prostate
Item
histologically confirmed adenocarcinoma of the prostate
boolean
C0007112 (UMLS CUI [1])
biochemical relapse
Item
biochemical relapse after primary radiation therapy or surgery
boolean
C2985506 (UMLS CUI [1])
testosterone level
Item
normal testosterone levels
boolean
C0523912 (UMLS CUI [1])
rising psa
Item
3 rising psa after nadir, with interval between psa determinations > 2 weeks
boolean
C0201544 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
local recurrence
Item
local recurrence by ct scan
boolean
C0027643 (UMLS CUI [1])
distant metastasis
Item
distant metastases by bone scan
boolean
C1269798 (UMLS CUI [1])
hypercalcemia
Item
hypercalcemia
boolean
C0020437 (UMLS CUI [1])
nephrolithiasis
Item
nephrolithiasis
boolean
C0392525 (UMLS CUI [1])
serum creatinine
Item
renal insufficiency (serum creatinine > 1.8 mg/dl)
boolean
C0201976 (UMLS CUI [1])
pancreatitis
Item
pancreatitis
boolean
C0030305 (UMLS CUI [1])
ulcer or gastrointestinal bleeding
Item
history of ulcer or gastrointestinal bleeding
boolean
C0030920 (UMLS CUI [1])
C0017181 (UMLS CUI [2])
hormone ablation therapy
Item
more than 6 months of hormone ablation therapy
boolean
C0279492 (UMLS CUI [1])
concurrent therapy for prostate cancer
Item
concurrent therapy for prostate cancer
boolean
C0009429 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
uncontrolled hypertension
Item
uncontrolled htn
boolean
C1868885 (UMLS CUI [1])
Myocardial Infarction, Cerebrovascular accident, Transient Ischemic Attack
Item
h/o mi, cva, tia
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
coronary disease/cerebrovascular disease
Item
known coronary disease/cerebrovascular disease
boolean
C0010068 (UMLS CUI [1])
C0007820 (UMLS CUI [2])
platelet count
Item
platelet counts <50
boolean
C0032181 (UMLS CUI [1])
anticoagulants
Item
patients on anticoagulants
boolean
C0003280 (UMLS CUI [1])
Lithium
Item
patients on lithium
boolean
C0023870 (UMLS CUI [1])

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