ID

38414

Beschrijving

18F FLT Imaging Studies of Treatment Response for Lung Cancer and Thymoma; ODM derived from: https://clinicaltrials.gov/show/NCT01610544

Link

https://clinicaltrials.gov/show/NCT01610544

Trefwoorden

Versies (1)
  1. 16-10-19 16-10-19 -
Houder van rechten

See clinicaltrials.gov

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16 oktober 2019

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Carcinoma, Non-Small-Cell Lung NCT01610544

Engels

Eligibility Carcinoma, Non-Small-Cell Lung NCT01610544

1 Formulieren  
Criteria
Beschrijving

Criteria

subjects with pathology proven lung cancer or thymic malignancy already enrolled in an nci treatment protocol usingazd6244 in nsclc and imc-a12, in thymoma.
Beschrijving

Carcinoma of lung | Malignant Neoplasm Thymic | Study Subject Participation Status | Treatment Protocols Specified | Non-Small Cell Lung Carcinoma | Thymoma

Datatype

boolean

Alias
UMLS CUI [1]
C0684249
UMLS CUI [2,1]
C0006826
UMLS CUI [2,2]
C0040113
UMLS CUI [3]
C2348568
UMLS CUI [4,1]
C0040808
UMLS CUI [4,2]
C0205369
UMLS CUI [5]
C0007131
UMLS CUI [6]
C0040100
participant must be 18 years or older
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ecog performance score of 0 to 2
Beschrijving

ECOG performance status

Datatype

boolean

Alias
UMLS CUI [1]
C1520224
ability to provide informed consent. all patients must sign a document of informed consent indicating their understanding of the investigational nature and risks of this study before any protocol related studies are performed.
Beschrijving

Informed Consent | Comprehension Study Protocol

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2,1]
C0162340
UMLS CUI [2,2]
C2348563
participants must not be pregnant or intend to become pregnant within 1 week of the last injection of (18)f flt
Beschrijving

Pregnancy Absent | Planned Pregnancy Absent | (18F) fluorothymidine Injection

Datatype

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0332197
UMLS CUI [2,1]
C0032992
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C1432709
UMLS CUI [3,2]
C1533685
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
known allergy to fluorothymidine
Beschrijving

Hypersensitivity (18F) fluorothymidine

Datatype

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C1432709
participants for whom enrollment would significantly delay (> 2 weeks) the scheduled standard of care therapy
Beschrijving

Enrollment Causing Delay Standard of Care

Datatype

boolean

Alias
UMLS CUI [1,1]
C1516879
UMLS CUI [1,2]
C0678227
UMLS CUI [1,3]
C0205421
UMLS CUI [1,4]
C2936643
participants with any coexisting medical or psychiatric condition that is likely to interfere with study procedures and/or results are excluded
Beschrijving

Comorbidity Interferes with Procedure Investigational | Mental condition Interferes with Procedure Investigational | Comorbidity Interferes with Research results | Mental condition Interferes with Research results

Datatype

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0184661
UMLS CUI [1,4]
C1517586
UMLS CUI [2,1]
C3840291
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C0184661
UMLS CUI [2,4]
C1517586
UMLS CUI [3,1]
C0009488
UMLS CUI [3,2]
C0521102
UMLS CUI [3,3]
C0683954
UMLS CUI [4,1]
C3840291
UMLS CUI [4,2]
C0521102
UMLS CUI [4,3]
C0683954
participants with severe claustrophobia not relieved by oral anxiolytic medication or patients weighing > 136 kg (weight limit for scanner table)
Beschrijving

Claustrophobia Severe | Anti-Anxiety Agents Unsuccessful | Body Weight Inappropriate Scanner Device

Datatype

boolean

Alias
UMLS CUI [1,1]
C0008909
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C0040616
UMLS CUI [2,2]
C1272705
UMLS CUI [3,1]
C0005910
UMLS CUI [3,2]
C1548788
UMLS CUI [3,3]
C1710020
other medical conditions deemed by the pi or associates to make the patient ineligible for protocol procedures
Beschrijving

Other medical condition Ineligibility Protocol procedure

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C1512714
UMLS CUI [1,3]
C2348563
UMLS CUI [1,4]
C0184661
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Similar models

Eligibility Carcinoma, Non-Small-Cell Lung NCT01610544

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
Carcinoma of lung | Malignant Neoplasm Thymic | Study Subject Participation Status | Treatment Protocols Specified | Non-Small Cell Lung Carcinoma | Thymoma
Item
subjects with pathology proven lung cancer or thymic malignancy already enrolled in an nci treatment protocol usingazd6244 in nsclc and imc-a12, in thymoma.
boolean
C0684249 (UMLS CUI [1])
C0006826 (UMLS CUI [2,1])
C0040113 (UMLS CUI [2,2])
C2348568 (UMLS CUI [3])
C0040808 (UMLS CUI [4,1])
C0205369 (UMLS CUI [4,2])
C0007131 (UMLS CUI [5])
C0040100 (UMLS CUI [6])
Age
Item
participant must be 18 years or older
boolean
C0001779 (UMLS CUI [1])
ECOG performance status
Item
ecog performance score of 0 to 2
boolean
C1520224 (UMLS CUI [1])
Informed Consent | Comprehension Study Protocol
Item
ability to provide informed consent. all patients must sign a document of informed consent indicating their understanding of the investigational nature and risks of this study before any protocol related studies are performed.
boolean
C0021430 (UMLS CUI [1])
C0162340 (UMLS CUI [2,1])
C2348563 (UMLS CUI [2,2])
Pregnancy Absent | Planned Pregnancy Absent | (18F) fluorothymidine Injection
Item
participants must not be pregnant or intend to become pregnant within 1 week of the last injection of (18)f flt
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0032992 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C1432709 (UMLS CUI [3,1])
C1533685 (UMLS CUI [3,2])
Item Group
C0680251 (UMLS CUI)
Hypersensitivity (18F) fluorothymidine
Item
known allergy to fluorothymidine
boolean
C0020517 (UMLS CUI [1,1])
C1432709 (UMLS CUI [1,2])
Enrollment Causing Delay Standard of Care
Item
participants for whom enrollment would significantly delay (> 2 weeks) the scheduled standard of care therapy
boolean
C1516879 (UMLS CUI [1,1])
C0678227 (UMLS CUI [1,2])
C0205421 (UMLS CUI [1,3])
C2936643 (UMLS CUI [1,4])
Comorbidity Interferes with Procedure Investigational | Mental condition Interferes with Procedure Investigational | Comorbidity Interferes with Research results | Mental condition Interferes with Research results
Item
participants with any coexisting medical or psychiatric condition that is likely to interfere with study procedures and/or results are excluded
boolean
C0009488 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0184661 (UMLS CUI [1,3])
C1517586 (UMLS CUI [1,4])
C3840291 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C0184661 (UMLS CUI [2,3])
C1517586 (UMLS CUI [2,4])
C0009488 (UMLS CUI [3,1])
C0521102 (UMLS CUI [3,2])
C0683954 (UMLS CUI [3,3])
C3840291 (UMLS CUI [4,1])
C0521102 (UMLS CUI [4,2])
C0683954 (UMLS CUI [4,3])
Claustrophobia Severe | Anti-Anxiety Agents Unsuccessful | Body Weight Inappropriate Scanner Device
Item
participants with severe claustrophobia not relieved by oral anxiolytic medication or patients weighing > 136 kg (weight limit for scanner table)
boolean
C0008909 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0040616 (UMLS CUI [2,1])
C1272705 (UMLS CUI [2,2])
C0005910 (UMLS CUI [3,1])
C1548788 (UMLS CUI [3,2])
C1710020 (UMLS CUI [3,3])
Other medical condition Ineligibility Protocol procedure
Item
other medical conditions deemed by the pi or associates to make the patient ineligible for protocol procedures
boolean
C3843040 (UMLS CUI [1,1])
C1512714 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
C0184661 (UMLS CUI [1,4])
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