ID

29480

Beschreibung

A Study of Triple-site Ventricular Pacing in Patients Who Have Not Responded to Conventional Dual Ventricular Site Cardiac Resynchronization Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT00941850

Link

https://clinicaltrials.gov/show/NCT00941850

Stichworte

  1. 03.04.18 03.04.18 -
  2. 03.04.18 03.04.18 -
Rechteinhaber

See clinicaltrials.gov

Hochgeladen am

3. April 2018

DOI

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Lizenz

Creative Commons BY-NC 3.0

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Eligibility Heart Failure NCT00941850

Eligibility Heart Failure NCT00941850

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
implanted with a crt device > 6 months previously according to current and conventional crt indications
Beschreibung

Implantation of CRT-D

Datentyp

boolean

Alias
UMLS CUI [1]
C1135480
device optimization > 1 months previously
Beschreibung

Medical Device Optimization

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0025080
UMLS CUI [1,2]
C2698650
aged 18yrs or older
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
able to attend outpatient follow up
Beschreibung

Outpatient Follow-up Able

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0029921
UMLS CUI [1,2]
C3274571
UMLS CUI [1,3]
C0085732
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
recent mi (<2 months)
Beschreibung

Myocardial Infarction

Datentyp

boolean

Alias
UMLS CUI [1]
C0027051
women who are pregnant or planning pregnancy
Beschreibung

Pregnancy | Pregnancy, Planned

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0032992
severe co morbid illness (where patients are not expected to survive duration of follow up period or where repeated outpatient visits may not be in best interest of patients)
Beschreibung

Comorbidity Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0009488
UMLS CUI [1,2]
C0205082
upgrade procedure is contraindicated for safety reasons.
Beschreibung

Medical contraindication Upgrade

Datentyp

boolean

Alias
UMLS CUI [1,1]
C1301624
UMLS CUI [1,2]
C3272274
class iv inotropic agents
Beschreibung

Inotropic agent Class

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0304509
UMLS CUI [1,2]
C0456387
patient unwilling to comply with required follow-up protocol including randomization scheme
Beschreibung

Protocol Compliance Unwilling

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0525058
UMLS CUI [1,2]
C0558080

Ähnliche Modelle

Eligibility Heart Failure NCT00941850

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Implantation of CRT-D
Item
implanted with a crt device > 6 months previously according to current and conventional crt indications
boolean
C1135480 (UMLS CUI [1])
Medical Device Optimization
Item
device optimization > 1 months previously
boolean
C0025080 (UMLS CUI [1,1])
C2698650 (UMLS CUI [1,2])
Age
Item
aged 18yrs or older
boolean
C0001779 (UMLS CUI [1])
Outpatient Follow-up Able
Item
able to attend outpatient follow up
boolean
C0029921 (UMLS CUI [1,1])
C3274571 (UMLS CUI [1,2])
C0085732 (UMLS CUI [1,3])
Item Group
C0680251 (UMLS CUI)
Myocardial Infarction
Item
recent mi (<2 months)
boolean
C0027051 (UMLS CUI [1])
Pregnancy | Pregnancy, Planned
Item
women who are pregnant or planning pregnancy
boolean
C0032961 (UMLS CUI [1])
C0032992 (UMLS CUI [2])
Comorbidity Severe
Item
severe co morbid illness (where patients are not expected to survive duration of follow up period or where repeated outpatient visits may not be in best interest of patients)
boolean
C0009488 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Medical contraindication Upgrade
Item
upgrade procedure is contraindicated for safety reasons.
boolean
C1301624 (UMLS CUI [1,1])
C3272274 (UMLS CUI [1,2])
Inotropic agent Class
Item
class iv inotropic agents
boolean
C0304509 (UMLS CUI [1,1])
C0456387 (UMLS CUI [1,2])
Protocol Compliance Unwilling
Item
patient unwilling to comply with required follow-up protocol including randomization scheme
boolean
C0525058 (UMLS CUI [1,1])
C0558080 (UMLS CUI [1,2])

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