Informationen:
Fehler:
ID
39397
Beschreibung
QuickOpt Chronic Study; ODM derived from: https://clinicaltrials.gov/show/NCT01172067
Link
https://clinicaltrials.gov/show/NCT01172067
Stichworte
Versionen (1)
- 07.01.20 07.01.20 -
Rechteinhaber
See clinicaltrials.gov
Hochgeladen am
7. Januar 2020
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 Heart Failure NCT01172067
Eligibility Heart Failure NCT01172067
- StudyEvent: Eligibility
Ähnliche Modelle
Eligibility Heart Failure NCT01172067
- StudyEvent: Eligibility
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Indication Cardiac Resynchronization Therapy Pacemaker (CRT-P) | Implantation Cardiac Resynchronization Therapy Pacemaker (CRT-P) | Other Coding
Item
• patient meets current crt-p indications and be implanted with an sjm crt-p device with v-v timing and a compatible lead system
boolean
C3146298 (UMLS CUI [1,1])
C1737639 (UMLS CUI [1,2])
C0021107 (UMLS CUI [2,1])
C1737639 (UMLS CUI [2,2])
C3846158 (UMLS CUI [3])
C1737639 (UMLS CUI [1,2])
C0021107 (UMLS CUI [2,1])
C1737639 (UMLS CUI [2,2])
C3846158 (UMLS CUI [3])
Informed Consent
Item
patient is able to provide written informed consent for study participation
boolean
C0021430 (UMLS CUI [1])
Activity Atrial Limited
Item
• patient has limited intrinsic atrial activity (≤ 40 bpm)
boolean
C0205177 (UMLS CUI [1,1])
C0018792 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
C0018792 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Persistent atrial fibrillation | Permanent atrial fibrillation
Item
patient has persistent or permanent af
boolean
C2585653 (UMLS CUI [1])
C2586056 (UMLS CUI [2])
C2586056 (UMLS CUI [2])
Second degree atrioventricular block | Complete atrioventricular block
Item
patient has a 2o or 3o heart block
boolean
C0264906 (UMLS CUI [1])
C0151517 (UMLS CUI [2])
C0151517 (UMLS CUI [2])
Life Expectancy
Item
patient's life expectancy is <12 months
boolean
C0023671 (UMLS CUI [1])
Age
Item
patient is <18 years old
boolean
C0001779 (UMLS CUI [1])
Pregnancy
Item
patient is pregnant
boolean
C0032961 (UMLS CUI [1])
Inotropic agent Intravenous
Item
patient is on iv inotropic agents
boolean
C0304509 (UMLS CUI [1,1])
C1522726 (UMLS CUI [1,2])
C1522726 (UMLS CUI [1,2])
Study Subject Participation Status | Investigational Medical Device | Investigational New Drugs
Item
patients who are ongoing other devices or agents study
boolean
C2348568 (UMLS CUI [1])
C2346570 (UMLS CUI [2])
C0013230 (UMLS CUI [3])
C2346570 (UMLS CUI [2])
C0013230 (UMLS CUI [3])
Heart Transplantation | Patient waiting for Heart Transplantation
Item
patients with heart transplanted or waiting for heart transplant
boolean
C0018823 (UMLS CUI [1])
C0542399 (UMLS CUI [2,1])
C0018823 (UMLS CUI [2,2])
C0542399 (UMLS CUI [2,1])
C0018823 (UMLS CUI [2,2])
Hypertrophic Cardiomyopathy
Item
patients with hypertrophic and obstructive cardiomyopathy
boolean
C0007194 (UMLS CUI [1])
Aortic Valve Stenosis Severe | Mitral Valve Stenosis Severe | Aortic Valve Insufficiency Severe | Mitral Valve Insufficiency Severe | Replacement Absent
Item
patients with severe aortic valve and mitral valve stenosis or regurgitation without replacement
boolean
C0003507 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C0026269 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0003504 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0026266 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C1410969 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])
C0205082 (UMLS CUI [1,2])
C0026269 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0003504 (UMLS CUI [3,1])
C0205082 (UMLS CUI [3,2])
C0026266 (UMLS CUI [4,1])
C0205082 (UMLS CUI [4,2])
C1410969 (UMLS CUI [5,1])
C0332197 (UMLS CUI [5,2])