ID

44466

Description

RESynchronizaTiOn theRapy and bEta-blocker Titration; ODM derived from: https://clinicaltrials.gov/show/NCT02173028

Link

https://clinicaltrials.gov/show/NCT02173028

Keywords

  1. 8/16/19 8/16/19 -
  2. 9/27/21 9/27/21 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

September 27, 2021

DOI

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License

Creative Commons BY 4.0

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Eligibility Beta Blocker Intolerance; NCT02173028

Eligibility Beta Blocker Intolerance; NCT02173028

Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients on optimal therapy for heart failure (diuretics, ace inhibitors and aldosterone antagonists), with stable dose in the previous month;
Description

Therapy Optimal Heart failure | Diuretics | Angiotensin-Converting Enzyme Inhibitors | Aldosterone Antagonists | Therapy Dose Stable

Data type

boolean

Alias
UMLS CUI [1,1]
C0087111
UMLS CUI [1,2]
C2698651
UMLS CUI [1,3]
C0018801
UMLS CUI [2]
C0012798
UMLS CUI [3]
C0003015
UMLS CUI [4]
C0002007
UMLS CUI [5,1]
C0087111
UMLS CUI [5,2]
C0178602
UMLS CUI [5,3]
C0205360
successfully implanted with crt-d according to current european society of cardiology (esc) guidelines;
Description

Implantation of CRT-D

Data type

boolean

Alias
UMLS CUI [1]
C1135480
new york heart association (nyha) functional class: ii, iii and iv;
Description

New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1]
C1275491
left ventricular ejection fraction (lvef) ≤ 35%;
Description

Left ventricular ejection fraction

Data type

boolean

Alias
UMLS CUI [1]
C0428772
duration of ventricular depolarization wave (qrs) ≥ 120ms (nyha iii or iv) or ≥
Description

QRS duration | New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1]
C0429025
UMLS CUI [2]
C1275491
150ms in nyha ii;
Description

QRS duration | New York Heart Association Classification

Data type

boolean

Alias
UMLS CUI [1]
C0429025
UMLS CUI [2]
C1275491
patients with chronic atrial fibrillation will be eligible for the study only if they undergo ablation ;
Description

Chronic atrial fibrillation | Ablation Required

Data type

boolean

Alias
UMLS CUI [1]
C0694539
UMLS CUI [2,1]
C0547070
UMLS CUI [2,2]
C1514873
18 years or above
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
failure to comply with the scheduled follow-up;
Description

Compliance failed | Follow-up Scheduled

Data type

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0231175
UMLS CUI [2,1]
C3274571
UMLS CUI [2,2]
C0205539
life expectancy less than 12 months ;
Description

Life Expectancy

Data type

boolean

Alias
UMLS CUI [1]
C0023671
pregnant women;
Description

Pregnancy

Data type

boolean

Alias
UMLS CUI [1]
C0032961
tricuspid valve mechanics;
Description

Tricuspid valve prosthesis

Data type

boolean

Alias
UMLS CUI [1]
C1322659
severe aortic stenosis or other valve disease ;
Description

Aortic stenosis, severe | Valvular disease

Data type

boolean

Alias
UMLS CUI [1]
C3806272
UMLS CUI [2]
C3258293
patients already receiving crt.
Description

Cardiac Resynchronization Therapy Pre-existing

Data type

boolean

Alias
UMLS CUI [1,1]
C1167956
UMLS CUI [1,2]
C2347662

Similar models

Eligibility Beta Blocker Intolerance; NCT02173028

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Therapy Optimal Heart failure | Diuretics | Angiotensin-Converting Enzyme Inhibitors | Aldosterone Antagonists | Therapy Dose Stable
Item
patients on optimal therapy for heart failure (diuretics, ace inhibitors and aldosterone antagonists), with stable dose in the previous month;
boolean
C0087111 (UMLS CUI [1,1])
C2698651 (UMLS CUI [1,2])
C0018801 (UMLS CUI [1,3])
C0012798 (UMLS CUI [2])
C0003015 (UMLS CUI [3])
C0002007 (UMLS CUI [4])
C0087111 (UMLS CUI [5,1])
C0178602 (UMLS CUI [5,2])
C0205360 (UMLS CUI [5,3])
Implantation of CRT-D
Item
successfully implanted with crt-d according to current european society of cardiology (esc) guidelines;
boolean
C1135480 (UMLS CUI [1])
New York Heart Association Classification
Item
new york heart association (nyha) functional class: ii, iii and iv;
boolean
C1275491 (UMLS CUI [1])
Left ventricular ejection fraction
Item
left ventricular ejection fraction (lvef) ≤ 35%;
boolean
C0428772 (UMLS CUI [1])
QRS duration | New York Heart Association Classification
Item
duration of ventricular depolarization wave (qrs) ≥ 120ms (nyha iii or iv) or ≥
boolean
C0429025 (UMLS CUI [1])
C1275491 (UMLS CUI [2])
QRS duration | New York Heart Association Classification
Item
150ms in nyha ii;
boolean
C0429025 (UMLS CUI [1])
C1275491 (UMLS CUI [2])
Chronic atrial fibrillation | Ablation Required
Item
patients with chronic atrial fibrillation will be eligible for the study only if they undergo ablation ;
boolean
C0694539 (UMLS CUI [1])
C0547070 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
Age
Item
18 years or above
boolean
C0001779 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Compliance failed | Follow-up Scheduled
Item
failure to comply with the scheduled follow-up;
boolean
C1321605 (UMLS CUI [1,1])
C0231175 (UMLS CUI [1,2])
C3274571 (UMLS CUI [2,1])
C0205539 (UMLS CUI [2,2])
Life Expectancy
Item
life expectancy less than 12 months ;
boolean
C0023671 (UMLS CUI [1])
Pregnancy
Item
pregnant women;
boolean
C0032961 (UMLS CUI [1])
Tricuspid valve prosthesis
Item
tricuspid valve mechanics;
boolean
C1322659 (UMLS CUI [1])
Aortic stenosis, severe | Valvular disease
Item
severe aortic stenosis or other valve disease ;
boolean
C3806272 (UMLS CUI [1])
C3258293 (UMLS CUI [2])
Cardiac Resynchronization Therapy Pre-existing
Item
patients already receiving crt.
boolean
C1167956 (UMLS CUI [1,1])
C2347662 (UMLS CUI [1,2])

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