ID

25064

Descripción

Radiation Therapy Followed by Surgery in High-Risk, Localized Carcinoma of the Prostate; ODM derived from: https://clinicaltrials.gov/show/NCT00691977

Link

https://clinicaltrials.gov/show/NCT00691977

Palabras clave

Versiones (1)
  1. 25/8/17 25/8/17 -
Subido en

25 de agosto de 2017

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Prostate Cancer NCT00691977

Inglés

Eligibility Prostate Cancer NCT00691977

1 formularios  
Inclusion Criteria
Descripción

Inclusion Criteria

Alias
UMLS CUI
C1512693
subjects must have biopsy-confirmed adenocarcinoma of the prostate.
Descripción

Adenocarcinoma of prostate

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0007112
subjects must have a negative bone scan.
Descripción

Bone scan Negative

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0203668
UMLS CUI [1,2]
C1513916
subjects must have "high-risk" prostate cancer, defined as:
Descripción

High risk of Prostate carcinoma

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332167
UMLS CUI [1,2]
C0600139
a. psa >/= 20, and/or b. gleason score (gs) >/= 8, and/or c. clinical stage t3 disease per ajcc staging manual, 6th edition; or d. at least two out of three of the following: psa 10-19.9, gs = 7, or clinical stage = t2b / t2c.
Descripción

PSA measurement | Gleason score | TNM clinical staging

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0201544
UMLS CUI [2]
C3203027
UMLS CUI [3]
C3258246
subjects must be medically fit to undergo surgery as determined by treating urologist.
Descripción

Fit Receive Operative Surgical Procedure

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0424576
UMLS CUI [1,2]
C1514756
UMLS CUI [1,3]
C0543467
subjects must be under 70 years of age.
Descripción

Age

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0001779
kps must be >/= 80.
Descripción

Karnofsky Performance Status

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0206065
subjects must not have a synchronous primary tumor, or a previous cancer unless disease free for >/= 5 years.
Descripción

Primary tumor Absent | Malignant Neoplasm Free of

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0677930
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0332296
subjects must not have had prior pelvic radiation therapy, chemotherapy, or androgen deprivation.
Descripción

Radiotherapy to pelvis Absent | Chemotherapy Absent | Antiandrogen therapy Absent

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C1536155
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0392920
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0279492
UMLS CUI [3,2]
C0332197
subjects must freely sign informed consent to enroll in the study.
Descripción

Informed Consent

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Descripción

Exclusion Criteria

Alias
UMLS CUI
C0680251
metastatic disease as demonstrated by bone scan, ct scan or mri of the pelvis, or chest x-ray.
Descripción

Neoplasm Metastasis Bone scan | Neoplasm Metastasis CT of Pelvis | Neoplasm Metastasis MRI of Pelvis | Neoplasm Metastasis Chest X-ray

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0027627
UMLS CUI [1,2]
C0203668
UMLS CUI [2,1]
C0027627
UMLS CUI [2,2]
C0412628
UMLS CUI [3,1]
C0027627
UMLS CUI [3,2]
C0203201
UMLS CUI [4,1]
C0027627
UMLS CUI [4,2]
C0039985
pathologically documented positive pelvic lymph nodes. if pre-operative ct scan or mri (ordered at the discretion of the treating physicians) demonstrates lymph nodes which are suspicious for involvement, then biopsy must be undertaken and nodes proven negative before patient can enroll on this trial.
Descripción

Pelvic lymph nodes Positive | CT scan Preoperative Pelvic lymph nodes | MRI Preoperative Pelvic lymph nodes | Biopsy Pelvic lymph nodes

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0729595
UMLS CUI [1,2]
C1514241
UMLS CUI [2,1]
C0040405
UMLS CUI [2,2]
C0445204
UMLS CUI [2,3]
C0729595
UMLS CUI [3,1]
C0024485
UMLS CUI [3,2]
C0445204
UMLS CUI [3,3]
C0729595
UMLS CUI [4,1]
C0005558
UMLS CUI [4,2]
C0729595
declared high-risk for anesthesia by attending anesthesiologist, cardiologist, or other physician.
Descripción

High risk Anesthesia

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0332167
UMLS CUI [1,2]
C0002903
history of prior pelvic radiation therapy.
Descripción

Radiotherapy to pelvis

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1536155
history of androgen deprivation therapy or chemotherapy.
Descripción

Antiandrogen therapy | Chemotherapy

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0279492
UMLS CUI [2]
C0392920
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Similar models

Eligibility Prostate Cancer NCT00691977

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
C1512693 (UMLS CUI)
Adenocarcinoma of prostate
Item
subjects must have biopsy-confirmed adenocarcinoma of the prostate.
boolean
C0007112 (UMLS CUI [1])
Bone scan Negative
Item
subjects must have a negative bone scan.
boolean
C0203668 (UMLS CUI [1,1])
C1513916 (UMLS CUI [1,2])
High risk of Prostate carcinoma
Item
subjects must have "high-risk" prostate cancer, defined as:
boolean
C0332167 (UMLS CUI [1,1])
C0600139 (UMLS CUI [1,2])
PSA measurement | Gleason score | TNM clinical staging
Item
a. psa >/= 20, and/or b. gleason score (gs) >/= 8, and/or c. clinical stage t3 disease per ajcc staging manual, 6th edition; or d. at least two out of three of the following: psa 10-19.9, gs = 7, or clinical stage = t2b / t2c.
boolean
C0201544 (UMLS CUI [1])
C3203027 (UMLS CUI [2])
C3258246 (UMLS CUI [3])
Fit Receive Operative Surgical Procedure
Item
subjects must be medically fit to undergo surgery as determined by treating urologist.
boolean
C0424576 (UMLS CUI [1,1])
C1514756 (UMLS CUI [1,2])
C0543467 (UMLS CUI [1,3])
Age
Item
subjects must be under 70 years of age.
boolean
C0001779 (UMLS CUI [1])
Karnofsky Performance Status
Item
kps must be >/= 80.
boolean
C0206065 (UMLS CUI [1])
Primary tumor Absent | Malignant Neoplasm Free of
Item
subjects must not have a synchronous primary tumor, or a previous cancer unless disease free for >/= 5 years.
boolean
C0677930 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006826 (UMLS CUI [2,1])
C0332296 (UMLS CUI [2,2])
Radiotherapy to pelvis Absent | Chemotherapy Absent | Antiandrogen therapy Absent
Item
subjects must not have had prior pelvic radiation therapy, chemotherapy, or androgen deprivation.
boolean
C1536155 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0392920 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0279492 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Informed Consent
Item
subjects must freely sign informed consent to enroll in the study.
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Neoplasm Metastasis Bone scan | Neoplasm Metastasis CT of Pelvis | Neoplasm Metastasis MRI of Pelvis | Neoplasm Metastasis Chest X-ray
Item
metastatic disease as demonstrated by bone scan, ct scan or mri of the pelvis, or chest x-ray.
boolean
C0027627 (UMLS CUI [1,1])
C0203668 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2,1])
C0412628 (UMLS CUI [2,2])
C0027627 (UMLS CUI [3,1])
C0203201 (UMLS CUI [3,2])
C0027627 (UMLS CUI [4,1])
C0039985 (UMLS CUI [4,2])
Pelvic lymph nodes Positive | CT scan Preoperative Pelvic lymph nodes | MRI Preoperative Pelvic lymph nodes | Biopsy Pelvic lymph nodes
Item
pathologically documented positive pelvic lymph nodes. if pre-operative ct scan or mri (ordered at the discretion of the treating physicians) demonstrates lymph nodes which are suspicious for involvement, then biopsy must be undertaken and nodes proven negative before patient can enroll on this trial.
boolean
C0729595 (UMLS CUI [1,1])
C1514241 (UMLS CUI [1,2])
C0040405 (UMLS CUI [2,1])
C0445204 (UMLS CUI [2,2])
C0729595 (UMLS CUI [2,3])
C0024485 (UMLS CUI [3,1])
C0445204 (UMLS CUI [3,2])
C0729595 (UMLS CUI [3,3])
C0005558 (UMLS CUI [4,1])
C0729595 (UMLS CUI [4,2])
High risk Anesthesia
Item
declared high-risk for anesthesia by attending anesthesiologist, cardiologist, or other physician.
boolean
C0332167 (UMLS CUI [1,1])
C0002903 (UMLS CUI [1,2])
Radiotherapy to pelvis
Item
history of prior pelvic radiation therapy.
boolean
C1536155 (UMLS CUI [1])
Antiandrogen therapy | Chemotherapy
Item
history of androgen deprivation therapy or chemotherapy.
boolean
C0279492 (UMLS CUI [1])
C0392920 (UMLS CUI [2])
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