Informationen:
Fehler:
ID
33293
Beschreibung
Safety and Efficacy of Oral Versus Intravenous Amiodarone in the Treatment of AF; ODM derived from: https://clinicaltrials.gov/show/NCT01817439
Link
https://clinicaltrials.gov/show/NCT01817439
Stichworte
Versionen (1)
- 04.12.18 04.12.18 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
4. Dezember 2018
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 Atrial Fibrillation NCT01817439
Eligibility Atrial Fibrillation NCT01817439
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Atrial Fibrillation NCT01817439
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Age
Item
over 18 years of age,
boolean
C0001779 (UMLS CUI [1])
Patient Admission Intensive care unit
Item
patients who will be admitted to the iccu / icu wards
boolean
C0030673 (UMLS CUI [1,1])
C0021708 (UMLS CUI [1,2])
C0021708 (UMLS CUI [1,2])
Atrial Fibrillation Onset Recent | Atrial Fibrillation Duration
Item
patients with recent onset of atrial fibrillation (duration < 48h).
boolean
C0004238 (UMLS CUI [1,1])
C0332162 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
C0332162 (UMLS CUI [1,2])
C0332185 (UMLS CUI [1,3])
C0004238 (UMLS CUI [2,1])
C0449238 (UMLS CUI [2,2])
Age
Item
age < 18 years
boolean
C0001779 (UMLS CUI [1])
Systolic Pressure
Item
baseline systolic blood pressure < 100 mm/hg
boolean
C0871470 (UMLS CUI [1])
Thyroid Disease
Item
known thyroid disease
boolean
C0040128 (UMLS CUI [1])
Serum potassium measurement
Item
serum potassium < 3.5 mmol/l
boolean
C0302353 (UMLS CUI [1])
Pretreatment Amiodarone
Item
pretreatment with amiodarone
boolean
C3539076 (UMLS CUI [1,1])
C0002598 (UMLS CUI [1,2])
C0002598 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
pregnant or lactating women.
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Study Subject Participation Status
Item
participation in other clinical trial.
boolean
C2348568 (UMLS CUI [1])