Information:
Fel:
ID
33395
Beskrivning
The Role of the Novel 99mTc-NC100692 Tracer in Patients at High Risk or Known Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT01503697
Länk
https://clinicaltrials.gov/show/NCT01503697
Nyckelord
Versioner (1)
- 2018-12-07 2018-12-07 -
Rättsinnehavare
See clinicaltrials.gov
Uppladdad den
7 december 2018
DOI
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Licens
Creative Commons BY 4.0
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Eligibility Breast Cancer NCT01503697
Eligibility Breast Cancer NCT01503697
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01503697
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datatyp
Alias
Age
Item
age ≥ 18 years.
boolean
C0001779 (UMLS CUI [1])
Breast Carcinoma Unknown | Lesion of breast Unclear | At high risk for breast cancer | BRCA Rearrangement | Protocol Treatment Arm Number
Item
patients with unknown breast cancer but unclear lesions in the breast on other modalities or patients at high risk for breast cancer (brca, familial)- arm 1
boolean
C0678222 (UMLS CUI [1,1])
C0439673 (UMLS CUI [1,2])
C0567489 (UMLS CUI [2,1])
C3845108 (UMLS CUI [2,2])
C4047809 (UMLS CUI [3])
C4055395 (UMLS CUI [4])
C1522541 (UMLS CUI [5,1])
C0237753 (UMLS CUI [5,2])
C0439673 (UMLS CUI [1,2])
C0567489 (UMLS CUI [2,1])
C3845108 (UMLS CUI [2,2])
C4047809 (UMLS CUI [3])
C4055395 (UMLS CUI [4])
C1522541 (UMLS CUI [5,1])
C0237753 (UMLS CUI [5,2])
Breast Carcinoma | Referral for FDG PET/CT TNM clinical staging | Referral for FDG PET/CT Restaging | Protocol Treatment Arm Number
Item
patients with breast cancer referred for 18-fdg pet-ct for staging or re-staging- arm 2
boolean
C0678222 (UMLS CUI [1])
C2585524 (UMLS CUI [2,1])
C4521453 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C2585524 (UMLS CUI [3,1])
C4521453 (UMLS CUI [3,2])
C4331246 (UMLS CUI [3,3])
C1522541 (UMLS CUI [4,1])
C0237753 (UMLS CUI [4,2])
C2585524 (UMLS CUI [2,1])
C4521453 (UMLS CUI [2,2])
C3258246 (UMLS CUI [2,3])
C2585524 (UMLS CUI [3,1])
C4521453 (UMLS CUI [3,2])
C4331246 (UMLS CUI [3,3])
C1522541 (UMLS CUI [4,1])
C0237753 (UMLS CUI [4,2])
Locally advanced breast cancer | Imaging | Protocol Treatment Arm Number
Item
study cohort will include 15 patients with locally advanced breast cancer. patients will undergo imaging prior to treatment and at its end- arm 3
boolean
C3495949 (UMLS CUI [1])
C0079595 (UMLS CUI [2])
C1522541 (UMLS CUI [3,1])
C0237753 (UMLS CUI [3,2])
C0079595 (UMLS CUI [2])
C1522541 (UMLS CUI [3,1])
C0237753 (UMLS CUI [3,2])
Informed Consent
Item
written signed informed consent to participate in the study.
boolean
C0021430 (UMLS CUI [1])
Pregnancy Absent | Breast Feeding Absent
Item
patients not pregnant or lactating.
boolean
C0032961 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0332197 (UMLS CUI [1,2])
C0006147 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
Breast Carcinoma Inconsistent Protocol Treatment Arm
Item
patients with breast cancer who do not fall into one of the three study arms.
boolean
C0678222 (UMLS CUI [1,1])
C0442809 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
C0442809 (UMLS CUI [1,2])
C1522541 (UMLS CUI [1,3])
Pregnancy | Breast Feeding
Item
pregnant or lactating females.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
participation in another investigational study.
boolean
C2348568 (UMLS CUI [1])