ID

22708

Descrizione

Magnetic Resonance Spectroscopic Imaging of the Prostate at 3 Tesla; ODM derived from: https://clinicaltrials.gov/show/NCT00588679

collegamento

https://clinicaltrials.gov/show/NCT00588679

Keywords

versioni (1)
  1. 10/06/17 10/06/17 -
Caricato su

10 giugno 2017

DOI

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Licenza

Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT00588679

Inglese

Eligibility Prostate Cancer NCT00588679

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient must have clinically suspected or biopsy proven prostate cancer. if a patient has been diagnosed with prostate cancer an official report of biopsy from mskcc or outside site is required. all outside pathology reports will be confirmed at mskcc.
Descrizione

prostate cancer, biopsy of prostate

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0194804
for those patients who have undergone prostate biopsy it is recommended that the interval between biopsy and protocol mri/mrsi should be at least 8 weeks.
Descrizione

interval between biopsy and protocol mri/mrsi

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1272706
UMLS CUI [1,2]
C0194804
UMLS CUI [1,3]
C1522706
UMLS CUI [1,4]
C0024485
patient is a potential surgical candidate for treatment of prostate cancer
Descrizione

prostate cancer, cancer surgery

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0600139
UMLS CUI [1,2]
C0920424
patient is willing to undergo an endorectal mri/mrsi exam on the 3.0t mr scanner
Descrizione

endorectal mri/mrsi

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3857139
UMLS CUI [1,2]
C1635662
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who because of general medical or psychiatric condition, or physiologic status unrelated to the presence of prostate cancer cannot give valid informed consent.
Descrizione

informed consent, comorbidity

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0009488
patients who are unwilling or unable to undergo mri/mrsi (including patients with contra-indications to mri such as the presence of cardiac pacemakers or non-compatible intracranial vascular clips.
Descrizione

unwilling/unable mri/mrsi, contraindication mri/mrsi

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0558080
UMLS CUI [1,2]
C1299582
UMLS CUI [1,3]
C1522706
UMLS CUI [1,4]
C0024485
UMLS CUI [2,1]
C1301624
UMLS CUI [2,2]
C1522706
UMLS CUI [2,3]
C0024485
UMLS CUI [2,4]
C0030163
UMLS CUI [2,5]
C1740525
patients who cannot tolerate or have contra-indications to endorectal coil insertion; for example, patients who have had a prior abdominoperineal resection of the rectum or have crohn's disease, patients with severe hemorrhoids, patients who have had prior radiation to the pelvis to treat a malignancy, or patients who have had minor rectal surgery within the previous 8 weeks.
Descrizione

toleration or contraindication to endorectal coil insertion, prior abdominoperineal resection of the rectum, crohn's disease, severe hemorrhoids, prior radiation to the pelvis, minor rectal surgery

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3857139
UMLS CUI [1,2]
C0680282
UMLS CUI [1,3]
C1301624
UMLS CUI [2]
C2349525
UMLS CUI [3]
C0010346
UMLS CUI [4]
C0019112
UMLS CUI [5,1]
C0279134
UMLS CUI [5,2]
C0030797
UMLS CUI [6]
C2066000
patients with an allergic reaction to latex.
Descrizione

hypersensitivity

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0023115
patients with a metallic hip implant or any other metallic implant or device in the pelvis that might distort local magnetic field and compromise quality of mri/mrsi.
Descrizione

metallic implant, mri

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C3693688
UMLS CUI [1,2]
C0024485
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Similar models

Eligibility Prostate Cancer NCT00588679

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
prostate cancer, biopsy of prostate
Item
patient must have clinically suspected or biopsy proven prostate cancer. if a patient has been diagnosed with prostate cancer an official report of biopsy from mskcc or outside site is required. all outside pathology reports will be confirmed at mskcc.
boolean
C0600139 (UMLS CUI [1,1])
C0194804 (UMLS CUI [1,2])
interval between biopsy and protocol mri/mrsi
Item
for those patients who have undergone prostate biopsy it is recommended that the interval between biopsy and protocol mri/mrsi should be at least 8 weeks.
boolean
C1272706 (UMLS CUI [1,1])
C0194804 (UMLS CUI [1,2])
C1522706 (UMLS CUI [1,3])
C0024485 (UMLS CUI [1,4])
prostate cancer, cancer surgery
Item
patient is a potential surgical candidate for treatment of prostate cancer
boolean
C0600139 (UMLS CUI [1,1])
C0920424 (UMLS CUI [1,2])
endorectal mri/mrsi
Item
patient is willing to undergo an endorectal mri/mrsi exam on the 3.0t mr scanner
boolean
C3857139 (UMLS CUI [1,1])
C1635662 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
informed consent, comorbidity
Item
patients who because of general medical or psychiatric condition, or physiologic status unrelated to the presence of prostate cancer cannot give valid informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0009488 (UMLS CUI [1,2])
unwilling/unable mri/mrsi, contraindication mri/mrsi
Item
patients who are unwilling or unable to undergo mri/mrsi (including patients with contra-indications to mri such as the presence of cardiac pacemakers or non-compatible intracranial vascular clips.
boolean
C0558080 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1522706 (UMLS CUI [1,3])
C0024485 (UMLS CUI [1,4])
C1301624 (UMLS CUI [2,1])
C1522706 (UMLS CUI [2,2])
C0024485 (UMLS CUI [2,3])
C0030163 (UMLS CUI [2,4])
C1740525 (UMLS CUI [2,5])
toleration or contraindication to endorectal coil insertion, prior abdominoperineal resection of the rectum, crohn's disease, severe hemorrhoids, prior radiation to the pelvis, minor rectal surgery
Item
patients who cannot tolerate or have contra-indications to endorectal coil insertion; for example, patients who have had a prior abdominoperineal resection of the rectum or have crohn's disease, patients with severe hemorrhoids, patients who have had prior radiation to the pelvis to treat a malignancy, or patients who have had minor rectal surgery within the previous 8 weeks.
boolean
C3857139 (UMLS CUI [1,1])
C0680282 (UMLS CUI [1,2])
C1301624 (UMLS CUI [1,3])
C2349525 (UMLS CUI [2])
C0010346 (UMLS CUI [3])
C0019112 (UMLS CUI [4])
C0279134 (UMLS CUI [5,1])
C0030797 (UMLS CUI [5,2])
C2066000 (UMLS CUI [6])
hypersensitivity
Item
patients with an allergic reaction to latex.
boolean
C0020517 (UMLS CUI [1,1])
C0023115 (UMLS CUI [1,2])
metallic implant, mri
Item
patients with a metallic hip implant or any other metallic implant or device in the pelvis that might distort local magnetic field and compromise quality of mri/mrsi.
boolean
C3693688 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
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