ID

18922

Description

Using Fiducial Markers to Aid in Prostate Cancer Radiation Treatment; ODM derived from: https://clinicaltrials.gov/show/NCT00061347

Link

https://clinicaltrials.gov/show/NCT00061347

Keywords

Versions (1)
  1. 11/24/16 11/24/16 -
Uploaded on

November 24, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT00061347

English

Eligibility Prostate Cancer NCT00061347

1 forms  
Criteria
Description

Criteria

pathologically confirmed adenocarcinoma of the prostate gland.
Description

Adenocarcinoma of prostate

Data type

boolean

Alias
UMLS CUI [1]
C0007112
age greater than or equal to 18 years.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
ecog performance status of 0 or 1.
Description

ECOG performance status

Data type

boolean

Alias
UMLS CUI [1]
C1520224
informed consent: all patients must sign a document of informed consent indicating their understanding of the investigational nature and risks of the study before any protocol related studies are performed (this does not include routine laboratory tests or imaging studies required to establish eligibility).
Description

Informed Consent | Laboratory Procedures | imaging studies

Data type

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0022885
UMLS CUI [3]
C1881134
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients with contraindication to transrectal needle placement:
Description

Medical contraindication Needle Placement Transrectal

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0027551
UMLS CUI [1,3]
C0441587
UMLS CUI [1,4]
C0205518
bleeding disorder;
Description

Blood Coagulation Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0005779
pt/ptt greater than 1.5.times the upper limit of normal;
Description

Prothrombin time assay | Partial Thromboplastin Time measurement

Data type

boolean

Alias
UMLS CUI [1]
C0033707
UMLS CUI [2]
C0030605
platelets less than 50k;
Description

Platelet Count measurement

Data type

boolean

Alias
UMLS CUI [1]
C0032181
artificial heart valve.
Description

artificial heart valve

Data type

boolean

Alias
UMLS CUI [1]
C1399223
patients with contraindications to mri:
Description

Medical contraindication Magnetic Resonance Imaging

Data type

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C0024485
patients weighing greater than 136 kg (weight limit for scanner table);
Description

Body Weight

Data type

boolean

Alias
UMLS CUI [1]
C0005910
patients with pacemakers, cerebral aneurysm clips, shrapnel injury, or implanted electronic devices.
Description

Artificial cardiac pacemaker | Cerebral aneurysm clip | Shrapnel injury | electronic cardiac device Implanted

Data type

boolean

Alias
UMLS CUI [1]
C0030163
UMLS CUI [2]
C3266151
UMLS CUI [3,1]
C0522670
UMLS CUI [3,2]
C3263723
UMLS CUI [4,1]
C2216239
UMLS CUI [4,2]
C0021102
patients with chronic inflammatory bowel disease.
Description

Chronic inflammatory bowel disease

Data type

boolean

Alias
UMLS CUI [1]
C1856359
patients with distant metastatic disease.
Description

Distant metastasis present

Data type

boolean

Alias
UMLS CUI [1]
C1275402
patients with a prior history of pelvic or prostate radiotherapy.
Description

Radiotherapy to pelvis | Radiotherapy to prostate

Data type

boolean

Alias
UMLS CUI [1]
C1536155
UMLS CUI [2]
C0948317
cognitively impaired patients who cannot give informed consent.
Description

Impaired cognition | Informed Consent Unable

Data type

boolean

Alias
UMLS CUI [1]
C0338656
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1299582
other medical conditions deemed by the pi or associates to make the patient ineligible for protocol investigations, procedures, and high-dose external beam radiotherapy.
Description

Medical condition Protocol Compliance Unable | Medical condition External Beam Radiation Therapy High dose Unable

Data type

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0525058
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C3843040
UMLS CUI [2,2]
C1517033
UMLS CUI [2,3]
C0444956
UMLS CUI [2,4]
C1299582
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Similar models

Eligibility Prostate Cancer NCT00061347

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Adenocarcinoma of prostate
Item
pathologically confirmed adenocarcinoma of the prostate gland.
boolean
C0007112 (UMLS CUI [1])
Age
Item
age greater than or equal to 18 years.
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ecog performance status of 0 or 1.
boolean
C1520224 (UMLS CUI [1])
Informed Consent | Laboratory Procedures | imaging studies
Item
informed consent: all patients must sign a document of informed consent indicating their understanding of the investigational nature and risks of the study before any protocol related studies are performed (this does not include routine laboratory tests or imaging studies required to establish eligibility).
boolean
C0021430 (UMLS CUI [1])
C0022885 (UMLS CUI [2])
C1881134 (UMLS CUI [3])
Item Group
C0680251 (UMLS CUI)
Medical contraindication Needle Placement Transrectal
Item
patients with contraindication to transrectal needle placement:
boolean
C1301624 (UMLS CUI [1,1])
C0027551 (UMLS CUI [1,2])
C0441587 (UMLS CUI [1,3])
C0205518 (UMLS CUI [1,4])
Blood Coagulation Disorders
Item
bleeding disorder;
boolean
C0005779 (UMLS CUI [1])
Prothrombin time assay | Partial Thromboplastin Time measurement
Item
pt/ptt greater than 1.5.times the upper limit of normal;
boolean
C0033707 (UMLS CUI [1])
C0030605 (UMLS CUI [2])
Platelet Count measurement
Item
platelets less than 50k;
boolean
C0032181 (UMLS CUI [1])
artificial heart valve
Item
artificial heart valve.
boolean
C1399223 (UMLS CUI [1])
Medical contraindication Magnetic Resonance Imaging
Item
patients with contraindications to mri:
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
Body Weight
Item
patients weighing greater than 136 kg (weight limit for scanner table);
boolean
C0005910 (UMLS CUI [1])
Artificial cardiac pacemaker | Cerebral aneurysm clip | Shrapnel injury | electronic cardiac device Implanted
Item
patients with pacemakers, cerebral aneurysm clips, shrapnel injury, or implanted electronic devices.
boolean
C0030163 (UMLS CUI [1])
C3266151 (UMLS CUI [2])
C0522670 (UMLS CUI [3,1])
C3263723 (UMLS CUI [3,2])
C2216239 (UMLS CUI [4,1])
C0021102 (UMLS CUI [4,2])
Chronic inflammatory bowel disease
Item
patients with chronic inflammatory bowel disease.
boolean
C1856359 (UMLS CUI [1])
Distant metastasis present
Item
patients with distant metastatic disease.
boolean
C1275402 (UMLS CUI [1])
Radiotherapy to pelvis | Radiotherapy to prostate
Item
patients with a prior history of pelvic or prostate radiotherapy.
boolean
C1536155 (UMLS CUI [1])
C0948317 (UMLS CUI [2])
Impaired cognition | Informed Consent Unable
Item
cognitively impaired patients who cannot give informed consent.
boolean
C0338656 (UMLS CUI [1])
C0021430 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Medical condition Protocol Compliance Unable | Medical condition External Beam Radiation Therapy High dose Unable
Item
other medical conditions deemed by the pi or associates to make the patient ineligible for protocol investigations, procedures, and high-dose external beam radiotherapy.
boolean
C3843040 (UMLS CUI [1,1])
C0525058 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C3843040 (UMLS CUI [2,1])
C1517033 (UMLS CUI [2,2])
C0444956 (UMLS CUI [2,3])
C1299582 (UMLS CUI [2,4])
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