Informationen:
Fehler:
ID
14794
Beschreibung
A Phase 2 Randomized, Double-blind Trial Evaluating the Effects of Chloroquine in Breast Cancer; ODM derived from: https://clinicaltrials.gov/show/NCT02333890
Link
https://clinicaltrials.gov/show/NCT02333890
Stichworte
Versionen (1)
- 28.04.16 28.04.16 -
Hochgeladen am
28. April 2016
DOI
Für eine Beantragung loggen Sie sich ein.
Lizenz
Creative Commons BY 4.0
Modell Kommentare :
Hier können Sie das Modell kommentieren. Über die Sprechblasen an den Itemgruppen und Items können Sie diese spezifisch kommentieren.
Itemgroup Kommentare für :
Item Kommentare für :
Um Formulare herunterzuladen müssen Sie angemeldet sein. Bitte loggen Sie sich ein oder registrieren Sie sich kostenlos.
Eligibility Breast Cancer NCT02333890
Eligibility Breast Cancer NCT02333890
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Breast Cancer NCT02333890
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Invasive breast carcinoma | Therapeutic procedure | Operative Surgical Procedures
Item
newly diagnosed histologically confirmed primary invasive breast cancer who is currently not undergoing any treatment while awaiting surgery in the next 2-6 weeks
boolean
C0853879 (UMLS CUI [1])
C0087111 (UMLS CUI [2])
C0543467 (UMLS CUI [3])
C0087111 (UMLS CUI [2])
C0543467 (UMLS CUI [3])
Malignant Neoplasms | Palpation | Diagnostic Imaging
Item
tumour ≥ 1.5 cm by palpation or imaging
boolean
C0006826 (UMLS CUI [1])
C0030247 (UMLS CUI [2])
C0011923 (UMLS CUI [3])
C0030247 (UMLS CUI [2])
C0011923 (UMLS CUI [3])
ECOG performance status
Item
ecog performance status 0-2
boolean
C1520224 (UMLS CUI [1])
Informed Consent
Item
written informed consent for the study
boolean
C0021430 (UMLS CUI [1])
Carcinoma breast stage IV
Item
known metastatic breast cancer
boolean
C0278488 (UMLS CUI [1])
Retinal Diseases | Disorder of eye | Unqualified visual loss, one eye
Item
history of pre-existing known retinal or ocular pathology patient has only one functioning eye
boolean
C0035309 (UMLS CUI [1])
C0015397 (UMLS CUI [2])
C0155066 (UMLS CUI [3])
C0015397 (UMLS CUI [2])
C0155066 (UMLS CUI [3])
Liver Dysfunction | AST serum level result | Serum Alanine Transaminase tests | Upper Limit of Normal
Item
abnormal hepatic function (serum ast or alt >3x upper limit of normal)
boolean
C0086565 (UMLS CUI [1])
C0428341 (UMLS CUI [2])
C0036828 (UMLS CUI [3])
C1519815 (UMLS CUI [4])
C0428341 (UMLS CUI [2])
C0036828 (UMLS CUI [3])
C1519815 (UMLS CUI [4])
Chloroquine | Hydroxychloroquine
Item
currently on cq or hcq or has been on the drug within the past 3 months for other conditions
boolean
C0008269 (UMLS CUI [1])
C0020336 (UMLS CUI [2])
C0020336 (UMLS CUI [2])
Psoriasis
Item
known history of psoriasis
boolean
C0033860 (UMLS CUI [1])
Epilepsy | Seizures
Item
known history of epilepsy or seizures
boolean
C0014544 (UMLS CUI [1])
C0036572 (UMLS CUI [2])
C0036572 (UMLS CUI [2])
Electrocardiogram Prolonged QT interval QTc interval
Item
electrocardiogram showing qt prolongation based on qtc interval >450 ms
boolean
C0013798 (UMLS CUI [1,1])
C0151878 (UMLS CUI [1,2])
C0489625 (UMLS CUI [1,3])
C0151878 (UMLS CUI [1,2])
C0489625 (UMLS CUI [1,3])
Compliance behavior Limited | Substance Use Disorders | Pathological drug intoxication
Item
inability to comply with a study protocol (abuse of alcohol, drugs or psychotic states)
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0038586 (UMLS CUI [2])
C0152129 (UMLS CUI [3])
C0439801 (UMLS CUI [1,2])
C0038586 (UMLS CUI [2])
C0152129 (UMLS CUI [3])
Pregnancy | Breast Feeding
Item
current known pregnancy or actively nursing
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Allergic Reaction Quinolones | Allergic Reaction Chloroquine
Item
allergic reactions to quinolones or cq
boolean
C1527304 (UMLS CUI [1,1])
C0034428 (UMLS CUI [1,2])
C1527304 (UMLS CUI [2,1])
C0008269 (UMLS CUI [2,2])
C0034428 (UMLS CUI [1,2])
C1527304 (UMLS CUI [2,1])
C0008269 (UMLS CUI [2,2])
Unable Informed Consent
Item
inability to consent.
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [1,2])