Informações:
Falhas:
ID
38223
Descrição
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
Palavras-chave
Versões (1)
- 29/09/2019 29/09/2019 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
29 de setembro de 2019
DOI
Para um pedido faça login.
Licença
Creative Commons BY 4.0
Comentários do modelo :
Aqui pode comentar o modelo. Pode comentá-lo especificamente através dos balões de texto nos grupos de itens e itens.
Comentários do grupo de itens para :
Comentários do item para :
Para descarregar formulários, precisa de ter uma sessão iniciada. Por favor faça login ou registe-se gratuitamente.
Eligibility Breast Cancer NCT02141373
Eligibility Breast Cancer NCT02141373
- StudyEvent: Eligibility
Similar models
Eligibility Breast Cancer NCT02141373
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
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])
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])
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])
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])
C0005779 (UMLS CUI [2])
Pregnancy | Breast Feeding
Item
pregnant or lactating patients
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
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])
C3665472 (UMLS CUI [1,2])