ID

35912

Description

Predicting Response to CRT Using Body Surface ECG Mapping; ODM derived from: https://clinicaltrials.gov/show/NCT01831518

Lien

https://clinicaltrials.gov/show/NCT01831518

Mots-clés

Versions (1)
  1. 03/04/2019 03/04/2019 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

3 avril 2019

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
Modèle Commentaires :

Ici, vous pouvez faire des commentaires sur le modèle. À partir des bulles de texte, vous pouvez laisser des commentaires spécifiques sur les groupes Item et les Item.

Retour au modèle Commentaires
Groupe Item commentaires pour :

Item commentaires pour :

Vous devez être connecté pour pouvoir télécharger des formulaires. Veuillez vous connecter ou s’inscrire gratuitement.

Eligibility Heart Failure NCT01831518

Anglais

Eligibility Heart Failure NCT01831518

1 Formulaires  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age >18 years old
Description

Age

Type de données

boolean

Alias
UMLS CUI [1]
C0001779
fulfils established clinical criteria for crt implantation (with or without a defibrillator)
Description

CRT Device Implantation | Implantation of CRT-D

Type de données

boolean

Alias
UMLS CUI [1,1]
C2936377
UMLS CUI [1,2]
C0021107
UMLS CUI [2]
C1135480
nyha class iii-iv heart failure (or nyha ii with nyha iii/iv symptoms in the preceding 12 months)
Description

Heart failure New York Heart Association Classification

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
lvef <35% (calculated using echocardiography or cardiac mr) at the time of implantation
Description

Left ventricular ejection fraction Echocardiography | Left ventricular ejection fraction MRI of Heart

Type de données

boolean

Alias
UMLS CUI [1,1]
C0428772
UMLS CUI [1,2]
C0013516
UMLS CUI [2,1]
C0428772
UMLS CUI [2,2]
C0412692
qrs duration > 130ms
Description

QRS duration

Type de données

boolean

Alias
UMLS CUI [1]
C0429025
optimal tolerated medical therapy for heart failure
Description

Therapeutic procedure Optimal Heart failure

Type de données

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2698651
UMLS CUI [1,3]
C0018801
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
severe, life threatening non cardiac disease
Description

Life threatening illness Severe | Exception Heart Disease

Type de données

boolean

Alias
UMLS CUI [1,1]
C3846017
UMLS CUI [1,2]
C0205082
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0018799
active malignant disease and recent (<5 years) malignant disease
Description

Malignant Neoplasms

Type de données

boolean

Alias
UMLS CUI [1]
C0006826
prior heart transplant
Description

Heart Transplantation

Type de données

boolean

Alias
UMLS CUI [1]
C0018823
recent history of unstable angina, acute coronary syndrome or myocardial infarction within three months of enrolment into the study
Description

Angina, Unstable | Acute Coronary Syndrome | Myocardial Infarction

Type de données

boolean

Alias
UMLS CUI [1]
C0002965
UMLS CUI [2]
C0948089
UMLS CUI [3]
C0027051
pregnancy
Description

Pregnancy

Type de données

boolean

Alias
UMLS CUI [1]
C0032961
failure to participate in consent process
Description

Informed Consent failed

Type de données

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C0231175
atrial fibrillation
Description

Atrial Fibrillation

Type de données

boolean

Alias
UMLS CUI [1]
C0004238
conventional pacemaker in situ
Description

Cardiac pacemaker in situ

Type de données

boolean

Alias
UMLS CUI [1]
C2712998
heart failure requiring constant intravenous therapy including diuretics and/or inotropes
Description

Heart failure Requirement Therapy Intravenous | Diuretics | Inotropic agent

Type de données

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0087111
UMLS CUI [1,4]
C1522726
UMLS CUI [2]
C0012798
UMLS CUI [3]
C0304509
recent revascularisation procedure i.e. coronary artery bypass grafting (cabg) or percutaneous coronary intervention (pci) within the last three months
Description

Revascularization | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention

Type de données

boolean

Alias
UMLS CUI [1]
C0581603
UMLS CUI [2]
C0010055
UMLS CUI [3]
C1532338
Retour au début de la page

Similar models

Eligibility Heart Failure NCT01831518

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age >18 years old
boolean
C0001779 (UMLS CUI [1])
CRT Device Implantation | Implantation of CRT-D
Item
fulfils established clinical criteria for crt implantation (with or without a defibrillator)
boolean
C2936377 (UMLS CUI [1,1])
C0021107 (UMLS CUI [1,2])
C1135480 (UMLS CUI [2])
Heart failure New York Heart Association Classification
Item
nyha class iii-iv heart failure (or nyha ii with nyha iii/iv symptoms in the preceding 12 months)
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Left ventricular ejection fraction Echocardiography | Left ventricular ejection fraction MRI of Heart
Item
lvef <35% (calculated using echocardiography or cardiac mr) at the time of implantation
boolean
C0428772 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
C0428772 (UMLS CUI [2,1])
C0412692 (UMLS CUI [2,2])
QRS duration
Item
qrs duration > 130ms
boolean
C0429025 (UMLS CUI [1])
Therapeutic procedure Optimal Heart failure
Item
optimal tolerated medical therapy for heart failure
boolean
C0087111 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Life threatening illness Severe | Exception Heart Disease
Item
severe, life threatening non cardiac disease
boolean
C3846017 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0018799 (UMLS CUI [2,2])
Malignant Neoplasms
Item
active malignant disease and recent (<5 years) malignant disease
boolean
C0006826 (UMLS CUI [1])
Heart Transplantation
Item
prior heart transplant
boolean
C0018823 (UMLS CUI [1])
Angina, Unstable | Acute Coronary Syndrome | Myocardial Infarction
Item
recent history of unstable angina, acute coronary syndrome or myocardial infarction within three months of enrolment into the study
boolean
C0002965 (UMLS CUI [1])
C0948089 (UMLS CUI [2])
C0027051 (UMLS CUI [3])
Pregnancy
Item
pregnancy
boolean
C0032961 (UMLS CUI [1])
Informed Consent failed
Item
failure to participate in consent process
boolean
C0021430 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
Atrial Fibrillation
Item
atrial fibrillation
boolean
C0004238 (UMLS CUI [1])
Cardiac pacemaker in situ
Item
conventional pacemaker in situ
boolean
C2712998 (UMLS CUI [1])
Heart failure Requirement Therapy Intravenous | Diuretics | Inotropic agent
Item
heart failure requiring constant intravenous therapy including diuretics and/or inotropes
boolean
C0018801 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0087111 (UMLS CUI [1,3])
C1522726 (UMLS CUI [1,4])
C0012798 (UMLS CUI [2])
C0304509 (UMLS CUI [3])
Revascularization | Coronary Artery Bypass Surgery | Percutaneous Coronary Intervention
Item
recent revascularisation procedure i.e. coronary artery bypass grafting (cabg) or percutaneous coronary intervention (pci) within the last three months
boolean
C0581603 (UMLS CUI [1])
C0010055 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
Retour au début de la page 

Contact

Utilisez ce formulaire pour les retours, les questions et les améliorations suggérées.

Les champs marqués d’un * sont obligatoires.

Aide

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