ID

36999

Beschreibung

Diffusion-weighted MRI for Individualized Radiation Therapy Planning of Lung Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02059889

Link

https://clinicaltrials.gov/show/NCT02059889

Stichworte

  1. 27.06.19 27.06.19 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

27. Juni 2019

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Recurrent Non-small Cell Lung Cancer NCT02059889

Eligibility Recurrent Non-small Cell Lung Cancer NCT02059889

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients must be able to undergo mri imaging; contrast application will be determined according to institutional guidelines; patients with lung cancer (stage ii - iiib) or locally recurrent lung cancer (following surgery) who are scheduled to receive external beam radiation therapy for at least 6 weeks
Beschreibung

Magnetic Resonance Imaging | MRI with contrast | Carcinoma of lung TNM clinical staging | Recurrent lung cancer Locally | Status post Operative Surgical Procedures | External Beam Radiation Therapy Scheduled

Datentyp

boolean

Alias
UMLS CUI [1]
C0024485
UMLS CUI [2]
C0202671
UMLS CUI [3,1]
C0684249
UMLS CUI [3,2]
C3258246
UMLS CUI [4,1]
C0862802
UMLS CUI [4,2]
C1517927
UMLS CUI [5,1]
C0231290
UMLS CUI [5,2]
C0543467
UMLS CUI [6,1]
C1517033
UMLS CUI [6,2]
C0205539
tumor visible on planning ct scan
Beschreibung

Tumor Visible CT scan

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0027651
UMLS CUI [1,2]
C0205379
UMLS CUI [1,3]
C0040405
negative pregnancy test for women of childbearing potential prior to study entry
Beschreibung

Childbearing Potential Pregnancy test negative

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0427780
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients requiring continuous supplemental oxygen
Beschreibung

Patient need for Supplemental oxygen Continuous

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0686904
UMLS CUI [1,2]
C4534306
UMLS CUI [1,3]
C0549178
patients with metal implants including pace makers and defibrillators
Beschreibung

Metallic implant | Artificial cardiac pacemaker | Defibrillators

Datentyp

boolean

Alias
UMLS CUI [1]
C3693688
UMLS CUI [2]
C0030163
UMLS CUI [3]
C0180307
patients with cerebral aneurysm clips or middle ear implant
Beschreibung

Aneurysm clip cerebral | Implant, Middle Ear

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0179977
UMLS CUI [1,2]
C0006104
UMLS CUI [2]
C0086454
patients with pain pump, a programmable shunt, or non-surgical metal (i.e. a foreign body)
Beschreibung

Pain pump | Shunt | Metallic foreign body

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0030193
UMLS CUI [1,2]
C0182537
UMLS CUI [2]
C0542331
UMLS CUI [3]
C1720389
claustrophobic patients
Beschreibung

Claustrophobia

Datentyp

boolean

Alias
UMLS CUI [1]
C0008909
prior radiotherapy to body area under investigation
Beschreibung

Prior radiation therapy Anatomic Site Investigational

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0279134
UMLS CUI [1,2]
C1515974
UMLS CUI [1,3]
C1517586
no vulnerable populations will be enrolled (prisoners, children, pregnant females, or institutionalized individuals)
Beschreibung

Vulnerable Populations | Prisoners | Children | Pregnant Women | Institutionalized Persons

Datentyp

boolean

Alias
UMLS CUI [1]
C0949366
UMLS CUI [2]
C0033167
UMLS CUI [3]
C0008059
UMLS CUI [4]
C0033011
UMLS CUI [5]
C0376326

Ähnliche Modelle

Eligibility Recurrent Non-small Cell Lung Cancer NCT02059889

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Magnetic Resonance Imaging | MRI with contrast | Carcinoma of lung TNM clinical staging | Recurrent lung cancer Locally | Status post Operative Surgical Procedures | External Beam Radiation Therapy Scheduled
Item
patients must be able to undergo mri imaging; contrast application will be determined according to institutional guidelines; patients with lung cancer (stage ii - iiib) or locally recurrent lung cancer (following surgery) who are scheduled to receive external beam radiation therapy for at least 6 weeks
boolean
C0024485 (UMLS CUI [1])
C0202671 (UMLS CUI [2])
C0684249 (UMLS CUI [3,1])
C3258246 (UMLS CUI [3,2])
C0862802 (UMLS CUI [4,1])
C1517927 (UMLS CUI [4,2])
C0231290 (UMLS CUI [5,1])
C0543467 (UMLS CUI [5,2])
C1517033 (UMLS CUI [6,1])
C0205539 (UMLS CUI [6,2])
Tumor Visible CT scan
Item
tumor visible on planning ct scan
boolean
C0027651 (UMLS CUI [1,1])
C0205379 (UMLS CUI [1,2])
C0040405 (UMLS CUI [1,3])
Childbearing Potential Pregnancy test negative
Item
negative pregnancy test for women of childbearing potential prior to study entry
boolean
C3831118 (UMLS CUI [1,1])
C0427780 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
Patient need for Supplemental oxygen Continuous
Item
patients requiring continuous supplemental oxygen
boolean
C0686904 (UMLS CUI [1,1])
C4534306 (UMLS CUI [1,2])
C0549178 (UMLS CUI [1,3])
Metallic implant | Artificial cardiac pacemaker | Defibrillators
Item
patients with metal implants including pace makers and defibrillators
boolean
C3693688 (UMLS CUI [1])
C0030163 (UMLS CUI [2])
C0180307 (UMLS CUI [3])
Aneurysm clip cerebral | Implant, Middle Ear
Item
patients with cerebral aneurysm clips or middle ear implant
boolean
C0179977 (UMLS CUI [1,1])
C0006104 (UMLS CUI [1,2])
C0086454 (UMLS CUI [2])
Pain pump | Shunt | Metallic foreign body
Item
patients with pain pump, a programmable shunt, or non-surgical metal (i.e. a foreign body)
boolean
C0030193 (UMLS CUI [1,1])
C0182537 (UMLS CUI [1,2])
C0542331 (UMLS CUI [2])
C1720389 (UMLS CUI [3])
Claustrophobia
Item
claustrophobic patients
boolean
C0008909 (UMLS CUI [1])
Prior radiation therapy Anatomic Site Investigational
Item
prior radiotherapy to body area under investigation
boolean
C0279134 (UMLS CUI [1,1])
C1515974 (UMLS CUI [1,2])
C1517586 (UMLS CUI [1,3])
Vulnerable Populations | Prisoners | Children | Pregnant Women | Institutionalized Persons
Item
no vulnerable populations will be enrolled (prisoners, children, pregnant females, or institutionalized individuals)
boolean
C0949366 (UMLS CUI [1])
C0033167 (UMLS CUI [2])
C0008059 (UMLS CUI [3])
C0033011 (UMLS CUI [4])
C0376326 (UMLS CUI [5])

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