ID

22046

Beschreibung

Paclitaxel/Carboplatin Plus Bevacizumab/Erlotinib in the First Line Treatment of Carcinoma of Unknown Primary Site; ODM derived from: https://clinicaltrials.gov/show/NCT00360360

Link

https://clinicaltrials.gov/show/NCT00360360

Stichworte

Versionen (1)
  1. 16.05.17 16.05.17 -
Hochgeladen am

16. Mai 2017

DOI

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Creative Commons BY 4.0
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Eligibility Neoplasm, Unknown Primary NCT00360360

Englisch

Eligibility Neoplasm, Unknown Primary NCT00360360

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
biopsy proven metastatic carcinoma with the following light microscopic histologies: adenocarcinoma, poorly differentiated carcinoma(must have immunoperoxidase stains to rule out lymphoma, neuroendocrine carcinoma),or poorly differentiated squamous carcinoma.
Beschreibung

Metastatic Carcinoma Biopsy | Histology Light microscopy | Adenocarcinoma | Poorly differentiated carcinoma Immunoperoxidase stain | Lymphoma Excluded | Neuroendocrine Carcinoma Excluded | Squamous cell carcinoma Poorly differentiated

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1384494
UMLS CUI [1,2]
C0005558
UMLS CUI [2,1]
C0344441
UMLS CUI [2,2]
C0430389
UMLS CUI [3]
C0001418
UMLS CUI [4,1]
C0741899
UMLS CUI [4,2]
C1441617
UMLS CUI [5,1]
C0024299
UMLS CUI [5,2]
C2828389
UMLS CUI [6,1]
C0206695
UMLS CUI [6,2]
C2828389
UMLS CUI [7,1]
C0007137
UMLS CUI [7,2]
C0205617
ecog performance status 0-1
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
no previous treatment with any systemic therapy
Beschreibung

systemic therapy

Datentyp

boolean

Alias
UMLS CUI [1]
C1515119
adequate kidney, liver and bone marrow function
Beschreibung

Renal function | Liver function | Bone Marrow function

Datentyp

boolean

Alias
UMLS CUI [1]
C0232804
UMLS CUI [2]
C0232741
UMLS CUI [3,1]
C0005953
UMLS CUI [3,2]
C0031843
be able to understand the nature of the study and give written informed consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
the following specific syndromes:
Beschreibung

Syndrome Specific

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0039082
UMLS CUI [1,2]
C0205369
neuroendocrine carcinoma
Beschreibung

Carcinoma, Neuroendocrine

Datentyp

boolean

Alias
UMLS CUI [1]
C0206695
women with adenocarcinoma isolated to axillary lymph nodes
Beschreibung

Gender | Adenocarcinoma Isolated Axillary lymph nodes

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0001418
UMLS CUI [2,2]
C0205409
UMLS CUI [2,3]
C0729594
women with adenocarcinoma isolated to peritoneal involvement
Beschreibung

Gender | Adenocarcinoma Isolated Involvement peritoneal

Datentyp

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2,1]
C0001418
UMLS CUI [2,2]
C0205409
UMLS CUI [2,3]
C1314939
UMLS CUI [2,4]
C0442034
carcinoma involving only one site with resectable tumors at that site
Beschreibung

Carcinoma Involving Site Single | Neoplasms Resectable Site

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007097
UMLS CUI [1,2]
C1314939
UMLS CUI [1,3]
C1515974
UMLS CUI [1,4]
C0205171
UMLS CUI [2,1]
C0027651
UMLS CUI [2,2]
C1514888
UMLS CUI [2,3]
C1515974
squamous carcinoma limited to cervical, supraclavicular, or inguinal lymph nodes
Beschreibung

Squamous cell carcinoma Limited Cervical lymph nodes | Squamous cell carcinoma Limited Supraclavicular lymph nodes | Squamous cell carcinoma Limited Inguinal lymph nodes

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0007137
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0588054
UMLS CUI [2,1]
C0007137
UMLS CUI [2,2]
C0439801
UMLS CUI [2,3]
C0229730
UMLS CUI [3,1]
C0007137
UMLS CUI [3,2]
C0439801
UMLS CUI [3,3]
C0729596
uncontrolled brain metastases and all patients with meningeal involvement
Beschreibung

Metastatic malignant neoplasm to brain Uncontrolled | Involvement meningeal

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0220650
UMLS CUI [1,2]
C0205318
UMLS CUI [2,1]
C1314939
UMLS CUI [2,2]
C0521400
women pregnant or lactating
Beschreibung

Pregnancy | Breast Feeding

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
clinically significant cardiovascular disease
Beschreibung

Cardiovascular Disease

Datentyp

boolean

Alias
UMLS CUI [1]
C0007222
history of myocardial infarction or stroke within 6 months
Beschreibung

Myocardial Infarction | Cerebrovascular accident

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
UMLS CUI [2]
C0038454
clinical history of hemoptysis or hematemesis
Beschreibung

Hemoptysis | Hematemesis

Datentyp

boolean

Alias
UMLS CUI [1]
C0019079
UMLS CUI [2]
C0018926
patients with peg tubes or g-tubes
Beschreibung

Percutaneous endoscopic tube | Gastrostomy tube

Datentyp

boolean

Alias
UMLS CUI [1]
C2985542
UMLS CUI [2]
C0150595
proteinuria
Beschreibung

Proteinuria

Datentyp

boolean

Alias
UMLS CUI [1]
C0033687
history of bleeding diathesis or coagulopathy
Beschreibung

Bleeding tendency | Blood Coagulation Disorders

Datentyp

boolean

Alias
UMLS CUI [1]
C1458140
UMLS CUI [2]
C0005779
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have. you can then decide if you wish to participate.
Beschreibung

Clinical Trial Eligibility Criteria Additional | Study Subject Participation Status

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1516637
UMLS CUI [1,2]
C1524062
UMLS CUI [2]
C2348568
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility Neoplasm, Unknown Primary NCT00360360

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Metastatic Carcinoma Biopsy | Histology Light microscopy | Adenocarcinoma | Poorly differentiated carcinoma Immunoperoxidase stain | Lymphoma Excluded | Neuroendocrine Carcinoma Excluded | Squamous cell carcinoma Poorly differentiated
Item
biopsy proven metastatic carcinoma with the following light microscopic histologies: adenocarcinoma, poorly differentiated carcinoma(must have immunoperoxidase stains to rule out lymphoma, neuroendocrine carcinoma),or poorly differentiated squamous carcinoma.
boolean
C1384494 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])
C0344441 (UMLS CUI [2,1])
C0430389 (UMLS CUI [2,2])
C0001418 (UMLS CUI [3])
C0741899 (UMLS CUI [4,1])
C1441617 (UMLS CUI [4,2])
C0024299 (UMLS CUI [5,1])
C2828389 (UMLS CUI [5,2])
C0206695 (UMLS CUI [6,1])
C2828389 (UMLS CUI [6,2])
C0007137 (UMLS CUI [7,1])
C0205617 (UMLS CUI [7,2])
ECOG performance status
Item
ecog performance status 0-1
boolean
C1520224 (UMLS CUI [1])
systemic therapy
Item
no previous treatment with any systemic therapy
boolean
C1515119 (UMLS CUI [1])
Renal function | Liver function | Bone Marrow function
Item
adequate kidney, liver and bone marrow function
boolean
C0232804 (UMLS CUI [1])
C0232741 (UMLS CUI [2])
C0005953 (UMLS CUI [3,1])
C0031843 (UMLS CUI [3,2])
Informed Consent
Item
be able to understand the nature of the study and give written informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Syndrome Specific
Item
the following specific syndromes:
boolean
C0039082 (UMLS CUI [1,1])
C0205369 (UMLS CUI [1,2])
Carcinoma, Neuroendocrine
Item
neuroendocrine carcinoma
boolean
C0206695 (UMLS CUI [1])
Gender | Adenocarcinoma Isolated Axillary lymph nodes
Item
women with adenocarcinoma isolated to axillary lymph nodes
boolean
C0079399 (UMLS CUI [1])
C0001418 (UMLS CUI [2,1])
C0205409 (UMLS CUI [2,2])
C0729594 (UMLS CUI [2,3])
Gender | Adenocarcinoma Isolated Involvement peritoneal
Item
women with adenocarcinoma isolated to peritoneal involvement
boolean
C0079399 (UMLS CUI [1])
C0001418 (UMLS CUI [2,1])
C0205409 (UMLS CUI [2,2])
C1314939 (UMLS CUI [2,3])
C0442034 (UMLS CUI [2,4])
Carcinoma Involving Site Single | Neoplasms Resectable Site
Item
carcinoma involving only one site with resectable tumors at that site
boolean
C0007097 (UMLS CUI [1,1])
C1314939 (UMLS CUI [1,2])
C1515974 (UMLS CUI [1,3])
C0205171 (UMLS CUI [1,4])
C0027651 (UMLS CUI [2,1])
C1514888 (UMLS CUI [2,2])
C1515974 (UMLS CUI [2,3])
Squamous cell carcinoma Limited Cervical lymph nodes | Squamous cell carcinoma Limited Supraclavicular lymph nodes | Squamous cell carcinoma Limited Inguinal lymph nodes
Item
squamous carcinoma limited to cervical, supraclavicular, or inguinal lymph nodes
boolean
C0007137 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0588054 (UMLS CUI [1,3])
C0007137 (UMLS CUI [2,1])
C0439801 (UMLS CUI [2,2])
C0229730 (UMLS CUI [2,3])
C0007137 (UMLS CUI [3,1])
C0439801 (UMLS CUI [3,2])
C0729596 (UMLS CUI [3,3])
Metastatic malignant neoplasm to brain Uncontrolled | Involvement meningeal
Item
uncontrolled brain metastases and all patients with meningeal involvement
boolean
C0220650 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C1314939 (UMLS CUI [2,1])
C0521400 (UMLS CUI [2,2])
Pregnancy | Breast Feeding
Item
women pregnant or lactating
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Cardiovascular Disease
Item
clinically significant cardiovascular disease
boolean
C0007222 (UMLS CUI [1])
Myocardial Infarction | Cerebrovascular accident
Item
history of myocardial infarction or stroke within 6 months
boolean
C0027051 (UMLS CUI [1])
C0038454 (UMLS CUI [2])
Hemoptysis | Hematemesis
Item
clinical history of hemoptysis or hematemesis
boolean
C0019079 (UMLS CUI [1])
C0018926 (UMLS CUI [2])
Percutaneous endoscopic tube | Gastrostomy tube
Item
patients with peg tubes or g-tubes
boolean
C2985542 (UMLS CUI [1])
C0150595 (UMLS CUI [2])
Proteinuria
Item
proteinuria
boolean
C0033687 (UMLS CUI [1])
Bleeding tendency | Blood Coagulation Disorders
Item
history of bleeding diathesis or coagulopathy
boolean
C1458140 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
Clinical Trial Eligibility Criteria Additional | Study Subject Participation Status
Item
please note: there are additional inclusion/exclusion criteria. the study center will determine if you meet all of the criteria. if you do not qualify for the trial, study personnel will explain the reasons. if you do qualify, study personnel will explain the trial in detail and answer any questions you may have. you can then decide if you wish to participate.
boolean
C1516637 (UMLS CUI [1,1])
C1524062 (UMLS CUI [1,2])
C2348568 (UMLS CUI [2])
Zum Seitenanfang zurückkehren 

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