Informations:
Erreur:
ID
38171
Description
Diffusion Weighted MR Imaging of the Breasts in Women at High Risk of Breast Cancer: A Pilot Study; ODM derived from: https://clinicaltrials.gov/show/NCT01938157
Lien
https://clinicaltrials.gov/show/NCT01938157
Mots-clés
Versions (1)
- 24/09/2019 24/09/2019 -
Détendeur de droits
See clinicaltrials.gov
Téléchargé le
24 septembre 2019
DOI
Pour une demande vous connecter.
Licence
Creative Commons BY 4.0
Modèle Commentaires :
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Eligibility Breast Cancer NCT01938157
Eligibility Breast Cancer NCT01938157
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT01938157
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Gender | High risk of Breast Carcinoma | MRI of breast Scheduled
Item
1. women at high-risk of breast cancer with an order for a clinical screening breast mri.
boolean
C0079399 (UMLS CUI [1])
C0332167 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C0344104 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
C0332167 (UMLS CUI [2,1])
C0678222 (UMLS CUI [2,2])
C0344104 (UMLS CUI [3,1])
C0205539 (UMLS CUI [3,2])
Gender Asymptomatic
Item
2. asymptomatic women.
boolean
C0079399 (UMLS CUI [1,1])
C0231221 (UMLS CUI [1,2])
C0231221 (UMLS CUI [1,2])
Informed Consent
Item
3. able to provide informed consent.
boolean
C0021430 (UMLS CUI [1])
Age
Item
4. at least 21 years of age.
boolean
C0001779 (UMLS CUI [1])
Symptoms | Palpable mass | Nipple discharge
Item
1. women with symptom such as palpable mass or nipple discharge.
boolean
C1457887 (UMLS CUI [1])
C0746412 (UMLS CUI [2])
C0149741 (UMLS CUI [3])
C0746412 (UMLS CUI [2])
C0149741 (UMLS CUI [3])
Medical contraindication MRI | Medical contraindication MRA | Artificial cardiac pacemaker | Aneurysm clip | Cochlear Implants | Metal foreign body in eye region
Item
2. women with mri/mra contraindications such as a cardiac pacemaker, and aneurysm clip, cochlear implants, and metal in the eyes.
boolean
C1301624 (UMLS CUI [1,1])
C0024485 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0243032 (UMLS CUI [2,2])
C0030163 (UMLS CUI [3])
C0179977 (UMLS CUI [4])
C0009199 (UMLS CUI [5])
C0562528 (UMLS CUI [6])
C0024485 (UMLS CUI [1,2])
C1301624 (UMLS CUI [2,1])
C0243032 (UMLS CUI [2,2])
C0030163 (UMLS CUI [3])
C0179977 (UMLS CUI [4])
C0009199 (UMLS CUI [5])
C0562528 (UMLS CUI [6])
Contrast media reaction Moderate Gadolinium DTPA Intravenous | Contrast media reaction Severe Gadolinium DTPA Intravenous
Item
3. women who have had a moderate or severe contrast reaction to intravenous gadolinium-dtpa.
boolean
C0853800 (UMLS CUI [1,1])
C0205081 (UMLS CUI [1,2])
C0060933 (UMLS CUI [1,3])
C1522726 (UMLS CUI [1,4])
C0853800 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0060933 (UMLS CUI [2,3])
C1522726 (UMLS CUI [2,4])
C0205081 (UMLS CUI [1,2])
C0060933 (UMLS CUI [1,3])
C1522726 (UMLS CUI [1,4])
C0853800 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0060933 (UMLS CUI [2,3])
C1522726 (UMLS CUI [2,4])
Informed Consent Unable
Item
4. women who are not able to give consent.
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,2])
Breast Carcinoma Newly Diagnosed
Item
5. women diagnosed with breast cancer within the last 6 months.
boolean
C0678222 (UMLS CUI [1,1])
C1518321 (UMLS CUI [1,2])
C1518321 (UMLS CUI [1,2])
Pregnancy
Item
6. women who are pregnant.
boolean
C0032961 (UMLS CUI [1])
Gender
Item
7. male patients.
boolean
C0079399 (UMLS CUI [1])