ID

38223

Description

Effectivenes of Cyanoacrylate (Glubran 2®) in Reducing Seroma Formation in Breast Cancer Patients Post-Axillary Dissection; ODM derived from: https://clinicaltrials.gov/show/NCT02141373

Link

https://clinicaltrials.gov/show/NCT02141373

Keywords

  1. 9/29/19 9/29/19 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 29, 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 NCT02141373

Eligibility Breast Cancer NCT02141373

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
the patient should be above 18 years old
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
the patients has node positive breast cancer
Description

Breast Carcinoma Lymph node positive

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0746319
the patient is eligible for axillary dissection in addition to a surgical intervention for the primary tumor
Description

Eligibility Excision of axillary lymph nodes | Eligibility Surgical intervention Primary tumor

Data type

boolean

Alias
UMLS CUI [1,1]
C1548635
UMLS CUI [1,2]
C0193867
UMLS CUI [2,1]
C1548635
UMLS CUI [2,2]
C0549433
UMLS CUI [2,3]
C0677930
patients whose sentinel lymph nodes test positive during surgery.
Description

Sentinel Lymph Node Positive | Time period Operative Surgical Procedure

Data type

boolean

Alias
UMLS CUI [1,1]
C1522495
UMLS CUI [1,2]
C1514241
UMLS CUI [2,1]
C1948053
UMLS CUI [2,2]
C0543467
the patient is willing to sign an informed consent to participation
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
platelet count is less than 100000
Description

Platelet Count measurement

Data type

boolean

Alias
UMLS CUI [1]
C0032181
obese patients with a bmi of more than 35
Description

Obesity | Body mass index

Data type

boolean

Alias
UMLS CUI [1]
C0028754
UMLS CUI [2]
C1305855
patients who need immediate breast reconstruction surgery
Description

Patient need for Mammaplasty Immediate

Data type

boolean

Alias
UMLS CUI [1,1]
C0686904
UMLS CUI [1,2]
C0085076
UMLS CUI [1,3]
C0205253
patients who are receiving anticoagulation therapy or have coagulation disorders
Description

Anticoagulation Therapy | Blood Coagulation Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0003281
UMLS CUI [2]
C0005779
pregnant or lactating patients
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
patients who are on steroid therapy
Description

Steroid therapy

Data type

boolean

Alias
UMLS CUI [1]
C0149783
patients who received chest radiotherapy
Description

Radiotherapy to thorax

Data type

boolean

Alias
UMLS CUI [1]
C4038705
patients who received neoadjuvant chemotherapy
Description

Neoadjuvant Chemotherapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0600558
UMLS CUI [1,2]
C3665472

Similar models

Eligibility Breast Cancer NCT02141373

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
the patient should be above 18 years old
boolean
C0001779 (UMLS CUI [1])
Breast Carcinoma Lymph node positive
Item
the patients has node positive breast cancer
boolean
C0678222 (UMLS CUI [1,1])
C0746319 (UMLS CUI [1,2])
Eligibility Excision of axillary lymph nodes | Eligibility Surgical intervention Primary tumor
Item
the patient is eligible for axillary dissection in addition to a surgical intervention for the primary tumor
boolean
C1548635 (UMLS CUI [1,1])
C0193867 (UMLS CUI [1,2])
C1548635 (UMLS CUI [2,1])
C0549433 (UMLS CUI [2,2])
C0677930 (UMLS CUI [2,3])
Sentinel Lymph Node Positive | Time period Operative Surgical Procedure
Item
patients whose sentinel lymph nodes test positive during surgery.
boolean
C1522495 (UMLS CUI [1,1])
C1514241 (UMLS CUI [1,2])
C1948053 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
Informed Consent
Item
the patient is willing to sign an informed consent to participation
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Platelet Count measurement
Item
platelet count is less than 100000
boolean
C0032181 (UMLS CUI [1])
Obesity | Body mass index
Item
obese patients with a bmi of more than 35
boolean
C0028754 (UMLS CUI [1])
C1305855 (UMLS CUI [2])
Patient need for Mammaplasty Immediate
Item
patients who need immediate breast reconstruction surgery
boolean
C0686904 (UMLS CUI [1,1])
C0085076 (UMLS CUI [1,2])
C0205253 (UMLS CUI [1,3])
Anticoagulation Therapy | Blood Coagulation Disorders
Item
patients who are receiving anticoagulation therapy or have coagulation disorders
boolean
C0003281 (UMLS CUI [1])
C0005779 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or lactating patients
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Steroid therapy
Item
patients who are on steroid therapy
boolean
C0149783 (UMLS CUI [1])
Radiotherapy to thorax
Item
patients who received chest radiotherapy
boolean
C4038705 (UMLS CUI [1])
Neoadjuvant Chemotherapy
Item
patients who received neoadjuvant chemotherapy
boolean
C0600558 (UMLS CUI [1,1])
C3665472 (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