ID

29459

Descrição

Correlation Of Respiratory Rate Level And Trend Evaluation in Heart Failure Patients; ODM derived from: https://clinicaltrials.gov/show/NCT00758121

Link

https://clinicaltrials.gov/show/NCT00758121

Palavras-chave

Versões (1)
  1. 27/03/2018 27/03/2018 -
Titular dos direitos

See clinicaltrials.gov

Transferido a

27 de março de 2018

DOI

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Licença

Creative Commons BY 4.0
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Eligibility Heart Failure NCT00758121

Inglês

Eligibility Heart Failure NCT00758121

1 Formulários  
Inclusion Criteria
Descrição

Inclusion Criteria

Alias
UMLS CUI
C1512693
implanted cognis device or future commercially available boston scientific crt-d, that contains the sensor trend for respiratory rate, with a right ventricular lead and left ventricular lead actively implanted
Descrição

Implantation of CRT-D | Ventricular Lead Right Implant | Ventricular Lead Left Implant

Tipo de dados

boolean

Alias
UMLS CUI [1]
C1135480
UMLS CUI [2,1]
C2825199
UMLS CUI [2,2]
C0205090
UMLS CUI [2,3]
C0021102
UMLS CUI [3,1]
C2825199
UMLS CUI [3,2]
C0205091
UMLS CUI [3,3]
C0021102
respiratory sensor programmed "on"
Descrição

Sensor respiratory

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0183210
UMLS CUI [1,2]
C0521346
classified as having nyha class iii heart failure documented, in the past 12 months
Descrição

Heart failure New York Heart Association Classification

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0018801
UMLS CUI [1,2]
C1275491
age 18 or above, or of legal age to give informed consent specific to state and national law
Descrição

Age | Age Legal

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0001779
UMLS CUI [2,1]
C0001779
UMLS CUI [2,2]
C1301860
willing and capable of providing informed consent, participating in all testing associated with this clinical investigation at an approved clinical investigational center and at the intervals defined by this protocol
Descrição

Informed Consent | Protocol Compliance

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0525058
Exclusion Criteria
Descrição

Exclusion Criteria

Alias
UMLS CUI
C0680251
inability or refusal to sign the patient informed consent
Descrição

Informed Consent Unable | Informed Consent Refused

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C1705116
inability or refusal to comply with the follow-up schedule
Descrição

Follow-up Compliance behavior Unable | Follow-up Compliance behavior Refused

Tipo de dados

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C1299582
UMLS CUI [2,1]
C3274571
UMLS CUI [2,2]
C1321605
UMLS CUI [2,3]
C1705116
patients that have received routinely scheduled intravenous inotropic therapy as part of their drug regimen within the past 90 days
Descrição

Pharmacotherapy | Inotropic agent Intravenous

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0013216
UMLS CUI [2,1]
C0304509
UMLS CUI [2,2]
C1522726
patients prescribed to positive airway pressure therapy
Descrição

Positive airway pressure therapy prescribed

Tipo de dados

boolean

Alias
UMLS CUI [1]
C3248586
a life expectancy of less than 180 days, per physician discretion
Descrição

Life Expectancy

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0023671
enrolled in any concurrent study without prior written approval from boston scientific crm
Descrição

Study Subject Participation Status

Tipo de dados

boolean

Alias
UMLS CUI [1]
C2348568
women who are pregnant or plan to become pregnant in the next twelve months
Descrição

Pregnancy | Pregnancy, Planned

Tipo de dados

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
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Similar models

Eligibility Heart Failure NCT00758121

1 Formulários
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Item Group
C1512693 (UMLS CUI)
Implantation of CRT-D | Ventricular Lead Right Implant | Ventricular Lead Left Implant
Item
implanted cognis device or future commercially available boston scientific crt-d, that contains the sensor trend for respiratory rate, with a right ventricular lead and left ventricular lead actively implanted
boolean
C1135480 (UMLS CUI [1])
C2825199 (UMLS CUI [2,1])
C0205090 (UMLS CUI [2,2])
C0021102 (UMLS CUI [2,3])
C2825199 (UMLS CUI [3,1])
C0205091 (UMLS CUI [3,2])
C0021102 (UMLS CUI [3,3])
Sensor respiratory
Item
respiratory sensor programmed "on"
boolean
C0183210 (UMLS CUI [1,1])
C0521346 (UMLS CUI [1,2])
Heart failure New York Heart Association Classification
Item
classified as having nyha class iii heart failure documented, in the past 12 months
boolean
C0018801 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
Age | Age Legal
Item
age 18 or above, or of legal age to give informed consent specific to state and national law
boolean
C0001779 (UMLS CUI [1])
C0001779 (UMLS CUI [2,1])
C1301860 (UMLS CUI [2,2])
Informed Consent | Protocol Compliance
Item
willing and capable of providing informed consent, participating in all testing associated with this clinical investigation at an approved clinical investigational center and at the intervals defined by this protocol
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Item Group
C0680251 (UMLS CUI)
Informed Consent Unable | Informed Consent Refused
Item
inability or refusal to sign the patient informed consent
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C1705116 (UMLS CUI [2,2])
Follow-up Compliance behavior Unable | Follow-up Compliance behavior Refused
Item
inability or refusal to comply with the follow-up schedule
boolean
C3274571 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C1299582 (UMLS CUI [1,3])
C3274571 (UMLS CUI [2,1])
C1321605 (UMLS CUI [2,2])
C1705116 (UMLS CUI [2,3])
Pharmacotherapy | Inotropic agent Intravenous
Item
patients that have received routinely scheduled intravenous inotropic therapy as part of their drug regimen within the past 90 days
boolean
C0013216 (UMLS CUI [1])
C0304509 (UMLS CUI [2,1])
C1522726 (UMLS CUI [2,2])
Positive airway pressure therapy prescribed
Item
patients prescribed to positive airway pressure therapy
boolean
C3248586 (UMLS CUI [1])
Life Expectancy
Item
a life expectancy of less than 180 days, per physician discretion
boolean
C0023671 (UMLS CUI [1])
Study Subject Participation Status
Item
enrolled in any concurrent study without prior written approval from boston scientific crm
boolean
C2348568 (UMLS CUI [1])
Pregnancy | Pregnancy, Planned
Item
women who are pregnant or plan to become pregnant in the next twelve months
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
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