ID

41990

Beschreibung

Hypofractionated Proton Radiation Therapy for Low and Intermediate Risk Prostate Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01368055

Link

https://clinicaltrials.gov/show/NCT01368055

Stichworte

Versionen (3)
  1. 17.01.19 17.01.19 -
  2. 27.05.19 27.05.19 -
  3. 15.03.21 15.03.21 - Dr. rer. medic Philipp Neuhaus
Rechteinhaber

University of Florida

Hochgeladen am

15. März 2021

DOI

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Lizenz

Creative Commons BY-NC 3.0
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Hypofractionated Radiotherapy in Prostate Cancer NCT01368055

Englisch

Eligibility Criteria

1 Formulare  
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
prostate cancer
Beschreibung

Prostate cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C0600139
gleason score 2-6 or 7
Beschreibung

Gleason score

Datentyp

boolean

Alias
UMLS CUI [1]
C3203027
psa ≤ 20 ng/ml.
Beschreibung

PSA level

Datentyp

boolean

Alias
UMLS CUI [1]
C0201544
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
previous prostate cancer surgery or pelvic radiation
Beschreibung

previous prostate cancer surgery or pelvic radiation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C0543467
UMLS CUI [1,3]
C0600139
UMLS CUI [2,1]
C0205156
UMLS CUI [2,2]
C0747411
prior/concurrent systemic chemotherapy for prostate cancer
Beschreibung

prior/concurrent systemic chemotherapy for prostate cancer

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C1883256
UMLS CUI [1,3]
C0600139
UMLS CUI [2,1]
C0521116
UMLS CUI [2,2]
C1883256
UMLS CUI [2,3]
C0600139
active inflammatory bowel disease (crohn's disease, diverticulitis or ulcerative colitis) affecting the rectum
Beschreibung

active inflammatory bowel disease (crohn's disease, diverticulitis or ulcerative colitis) affecting the rectum

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205177
UMLS CUI [1,2]
C0021390
UMLS CUI [1,3]
C0392760
UMLS CUI [1,4]
C0034896
UMLS CUI [2,1]
C0205177
UMLS CUI [2,2]
C0010346
UMLS CUI [2,3]
C0392760
UMLS CUI [2,4]
C0034896
UMLS CUI [3,1]
C0205177
UMLS CUI [3,2]
C0012813
UMLS CUI [3,3]
C0392760
UMLS CUI [3,4]
C0034896
UMLS CUI [4,1]
C0205177
UMLS CUI [4,2]
C0009324
UMLS CUI [4,3]
C0392760
UMLS CUI [4,4]
C0034896
history of hip replacement
Beschreibung

history of hip replacement

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0205156
UMLS CUI [1,2]
C0392806
prior intrapelvic surgery
Beschreibung

prior intrapelvic surgery

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0744961
UMLS CUI [1,2]
C4048192
taking Saw Palmetto or methotrexate and unable or unwilling to discontinue its uses during radiation
Beschreibung

taking Saw Palmetto or methotrexate and unable or unwilling to discontinue its uses during radiation

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0771607
UMLS CUI [1,2]
C1548265
UMLS CUI [1,3]
C0347984
UMLS CUI [1,4]
C1522449
UMLS CUI [2,1]
C0771607
UMLS CUI [2,2]
C0558080
UMLS CUI [2,3]
C1444662
UMLS CUI [2,4]
C0347984
UMLS CUI [2,5]
C1522449
UMLS CUI [3,1]
C0025677
UMLS CUI [3,2]
C1548265
UMLS CUI [3,3]
C0347984
UMLS CUI [3,4]
C1522449
UMLS CUI [4,1]
C0025677
UMLS CUI [4,2]
C0558080
UMLS CUI [4,3]
C1444662
UMLS CUI [4,4]
C0347984
UMLS CUI [4,5]
C1522449
receiving continuous and current anticoagulation with warfarin sodium (coumadin), clopidogrel bisulfate (plavix), dabigatran etexilate mesylate (pradaxa),enoxaparin sodium (lovenox), or aspirin/er dipyridamole (aggrenox)
Beschreibung

continuous and current anticoagulation with warfarin, clopidogrel, dabigatran, enoxaparin or aspirin/dipyridamole

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0003280
UMLS CUI [1,2]
C0549178
UMLS CUI [1,3]
C0521116
UMLS CUI [2,1]
C0376218
UMLS CUI [2,2]
C0549178
UMLS CUI [2,3]
C0521116
UMLS CUI [3,1]
C0772326
UMLS CUI [3,2]
C0549178
UMLS CUI [3,3]
C0521116
UMLS CUI [4,1]
C1571583
UMLS CUI [4,2]
C0549178
UMLS CUI [4,3]
C0521116
UMLS CUI [5,1]
C0206460
UMLS CUI [5,2]
C0549178
UMLS CUI [5,3]
C0521116
UMLS CUI [6,1]
C0732279
UMLS CUI [6,2]
C0549178
UMLS CUI [6,3]
C0521116
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Ähnliche Modelle

Eligibility Criteria

1 Formulare
  1. StudyEvent: Eligibility
    1. Eligibility Criteria
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Prostate cancer
Item
prostate cancer
boolean
C0600139 (UMLS CUI [1])
Gleason score
Item
gleason score 2-6 or 7
boolean
C3203027 (UMLS CUI [1])
PSA level
Item
psa ≤ 20 ng/ml.
boolean
C0201544 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
previous prostate cancer surgery or pelvic radiation
Item
previous prostate cancer surgery or pelvic radiation
boolean
C0205156 (UMLS CUI [1,1])
C0543467 (UMLS CUI [1,2])
C0600139 (UMLS CUI [1,3])
C0205156 (UMLS CUI [2,1])
C0747411 (UMLS CUI [2,2])
prior/concurrent systemic chemotherapy for prostate cancer
Item
prior/concurrent systemic chemotherapy for prostate cancer
boolean
C0205156 (UMLS CUI [1,1])
C1883256 (UMLS CUI [1,2])
C0600139 (UMLS CUI [1,3])
C0521116 (UMLS CUI [2,1])
C1883256 (UMLS CUI [2,2])
C0600139 (UMLS CUI [2,3])
active inflammatory bowel disease (crohn's disease, diverticulitis or ulcerative colitis) affecting the rectum
Item
active inflammatory bowel disease (crohn's disease, diverticulitis or ulcerative colitis) affecting the rectum
boolean
C0205177 (UMLS CUI [1,1])
C0021390 (UMLS CUI [1,2])
C0392760 (UMLS CUI [1,3])
C0034896 (UMLS CUI [1,4])
C0205177 (UMLS CUI [2,1])
C0010346 (UMLS CUI [2,2])
C0392760 (UMLS CUI [2,3])
C0034896 (UMLS CUI [2,4])
C0205177 (UMLS CUI [3,1])
C0012813 (UMLS CUI [3,2])
C0392760 (UMLS CUI [3,3])
C0034896 (UMLS CUI [3,4])
C0205177 (UMLS CUI [4,1])
C0009324 (UMLS CUI [4,2])
C0392760 (UMLS CUI [4,3])
C0034896 (UMLS CUI [4,4])
history of hip replacement
Item
history of hip replacement
boolean
C0205156 (UMLS CUI [1,1])
C0392806 (UMLS CUI [1,2])
prior intrapelvic surgery
Item
prior intrapelvic surgery
boolean
C0744961 (UMLS CUI [1,1])
C4048192 (UMLS CUI [1,2])
taking Saw Palmetto or methotrexate and unable or unwilling to discontinue its uses during radiation
Item
taking Saw Palmetto or methotrexate and unable or unwilling to discontinue its uses during radiation
boolean
C0771607 (UMLS CUI [1,1])
C1548265 (UMLS CUI [1,2])
C0347984 (UMLS CUI [1,3])
C1522449 (UMLS CUI [1,4])
C0771607 (UMLS CUI [2,1])
C0558080 (UMLS CUI [2,2])
C1444662 (UMLS CUI [2,3])
C0347984 (UMLS CUI [2,4])
C1522449 (UMLS CUI [2,5])
C0025677 (UMLS CUI [3,1])
C1548265 (UMLS CUI [3,2])
C0347984 (UMLS CUI [3,3])
C1522449 (UMLS CUI [3,4])
C0025677 (UMLS CUI [4,1])
C0558080 (UMLS CUI [4,2])
C1444662 (UMLS CUI [4,3])
C0347984 (UMLS CUI [4,4])
C1522449 (UMLS CUI [4,5])
continuous and current anticoagulation with warfarin, clopidogrel, dabigatran, enoxaparin or aspirin/dipyridamole
Item
receiving continuous and current anticoagulation with warfarin sodium (coumadin), clopidogrel bisulfate (plavix), dabigatran etexilate mesylate (pradaxa),enoxaparin sodium (lovenox), or aspirin/er dipyridamole (aggrenox)
boolean
C0003280 (UMLS CUI [1,1])
C0549178 (UMLS CUI [1,2])
C0521116 (UMLS CUI [1,3])
C0376218 (UMLS CUI [2,1])
C0549178 (UMLS CUI [2,2])
C0521116 (UMLS CUI [2,3])
C0772326 (UMLS CUI [3,1])
C0549178 (UMLS CUI [3,2])
C0521116 (UMLS CUI [3,3])
C1571583 (UMLS CUI [4,1])
C0549178 (UMLS CUI [4,2])
C0521116 (UMLS CUI [4,3])
C0206460 (UMLS CUI [5,1])
C0549178 (UMLS CUI [5,2])
C0521116 (UMLS CUI [5,3])
C0732279 (UMLS CUI [6,1])
C0549178 (UMLS CUI [6,2])
C0521116 (UMLS CUI [6,3])
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