ID

38201

Description

Intraoperative Radiation Therapy in Early Stage Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02266602

Link

https://clinicaltrials.gov/show/NCT02266602

Keywords

  1. 9/26/19 9/26/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 26, 2019

DOI

To request one please log in.

License

Creative Commons BY 4.0

Model comments :

You can comment on the data model here. Via the speech bubbles at the itemgroups and items you can add comments to those specificially.

Itemgroup comments for :

Item comments for :

In order to download data models you must be logged in. Please log in or register for free.

Eligibility Breast Cancer NCT02266602

Eligibility Breast Cancer NCT02266602

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
general inclusion criteria
Description

Inclusion criteria General

Data type

boolean

Alias
UMLS CUI [1,1]
C1512693
UMLS CUI [1,2]
C0205246
1. age ≥ 45 years.
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
2. clinical stage tis, t1, t2 (≤ 3cm), n0, m0 (ajcc classification).
Description

TNM Breast tumor staging

Data type

boolean

Alias
UMLS CUI [1]
C0474926
3. invasive ductal or lobular carcinoma, dcis and/ or pleomorphic lobular carcinoma in situ.
Description

Invasive Ductal Breast Carcinoma | Invasive Lobular Breast Carcinoma | DCIS | Pleomorphic lobular carcinoma in situ

Data type

boolean

Alias
UMLS CUI [1]
C1134719
UMLS CUI [2]
C0279565
UMLS CUI [3]
C0007124
UMLS CUI [4]
C2919327
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. scleroderma, systemic sclerosis and active lupus.
Description

Scleroderma | Systemic Sclerosis | Lupus Erythematosus

Data type

boolean

Alias
UMLS CUI [1]
C0011644
UMLS CUI [2]
C0036421
UMLS CUI [3]
C0409974
2. participation in an investigational drug or device study.
Description

Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device

Data type

boolean

Alias
UMLS CUI [1]
C2348568
UMLS CUI [2]
C0013230
UMLS CUI [3]
C2346570
3. previous ipsilateral radiation to the thorax or breast.
Description

Prior radiation therapy Ipsilateral Chest | Prior radiation therapy Ipsilateral Breast

Data type

boolean

Alias
UMLS CUI [1,1]
C0279134
UMLS CUI [1,2]
C0441989
UMLS CUI [1,3]
C0817096
UMLS CUI [2,1]
C0279134
UMLS CUI [2,2]
C0441989
UMLS CUI [2,3]
C0006141
4. multifocal breast cancer.
Description

Multifocal breast carcinoma

Data type

boolean

Alias
UMLS CUI [1]
C2986662
5. pregnant patients.
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
6. patient not competent to provide informed consent.
Description

Informed Consent incompetent

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0231190
7. neoadjuvant systemic therapy.
Description

Neoadjuvant Therapy Systemic

Data type

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C0205373
8. lymphovascular invasion on biopsy pathology
Description

Lymphatic Invasion Biopsy

Data type

boolean

Alias
UMLS CUI [1,1]
C1708790
UMLS CUI [1,2]
C0005558

Similar models

Eligibility Breast Cancer NCT02266602

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Inclusion criteria General
Item
general inclusion criteria
boolean
C1512693 (UMLS CUI [1,1])
C0205246 (UMLS CUI [1,2])
Age
Item
1. age ≥ 45 years.
boolean
C0001779 (UMLS CUI [1])
TNM Breast tumor staging
Item
2. clinical stage tis, t1, t2 (≤ 3cm), n0, m0 (ajcc classification).
boolean
C0474926 (UMLS CUI [1])
Invasive Ductal Breast Carcinoma | Invasive Lobular Breast Carcinoma | DCIS | Pleomorphic lobular carcinoma in situ
Item
3. invasive ductal or lobular carcinoma, dcis and/ or pleomorphic lobular carcinoma in situ.
boolean
C1134719 (UMLS CUI [1])
C0279565 (UMLS CUI [2])
C0007124 (UMLS CUI [3])
C2919327 (UMLS CUI [4])
Item Group
C0680251 (UMLS CUI)
Scleroderma | Systemic Sclerosis | Lupus Erythematosus
Item
1. scleroderma, systemic sclerosis and active lupus.
boolean
C0011644 (UMLS CUI [1])
C0036421 (UMLS CUI [2])
C0409974 (UMLS CUI [3])
Study Subject Participation Status | Investigational New Drugs | Investigational Medical Device
Item
2. participation in an investigational drug or device study.
boolean
C2348568 (UMLS CUI [1])
C0013230 (UMLS CUI [2])
C2346570 (UMLS CUI [3])
Prior radiation therapy Ipsilateral Chest | Prior radiation therapy Ipsilateral Breast
Item
3. previous ipsilateral radiation to the thorax or breast.
boolean
C0279134 (UMLS CUI [1,1])
C0441989 (UMLS CUI [1,2])
C0817096 (UMLS CUI [1,3])
C0279134 (UMLS CUI [2,1])
C0441989 (UMLS CUI [2,2])
C0006141 (UMLS CUI [2,3])
Multifocal breast carcinoma
Item
4. multifocal breast cancer.
boolean
C2986662 (UMLS CUI [1])
Pregnancy
Item
5. pregnant patients.
boolean
C0032961 (UMLS CUI [1])
Informed Consent incompetent
Item
6. patient not competent to provide informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0231190 (UMLS CUI [1,2])
Neoadjuvant Therapy Systemic
Item
7. neoadjuvant systemic therapy.
boolean
C0600558 (UMLS CUI [1,1])
C0205373 (UMLS CUI [1,2])
Lymphatic Invasion Biopsy
Item
8. lymphovascular invasion on biopsy pathology
boolean
C1708790 (UMLS CUI [1,1])
C0005558 (UMLS CUI [1,2])

Please use this form for feedback, questions and suggestions for improvements.

Fields marked with * are required.

Do you need help on how to use the search function? Please watch the corresponding tutorial video for more details and learn how to use the search function most efficiently.

Watch Tutorial