ID

17365

Beschreibung

Study to Evaluate the Performance and Safety of Expedial and Compare it to Expanded Polytetrafluoroethylene (ePTFE) Vascular Access Grafts; ODM derived from: https://clinicaltrials.gov/show/NCT00131872

Link

https://clinicaltrials.gov/show/NCT00131872

Stichworte

Versionen (3)
  1. 09.09.16 09.09.16 -
  2. 02.09.21 02.09.21 -
  3. 20.09.21 20.09.21 -
Hochgeladen am

9. September 2016

DOI

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Lizenz

Creative Commons BY 4.0
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Eligibility End Stage Renal Disease NCT00131872

Englisch

Eligibility End Stage Renal Disease NCT00131872

1 Formulare  
Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
patient has chronic renal failure and requires vascular access for hemodialysis
Beschreibung

Chronic Kidney Failure Requirement vascular access Hemodialysis

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0022661
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0750138
UMLS CUI [1,4]
C0019004
patient has given informed consent to participate in the trial and is willing to comply with the study protocol
Beschreibung

Informed Consent | Protocol Compliance

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
UMLS CUI [2]
C0525058
patient is male or female, 18 years of age or older
Beschreibung

Age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
the vascular access graft can be placed in the upper extremity (forearm, including across the elbow, or upper arm)
Beschreibung

Insertion of graft for vascular access Upper Extremity | Insertion of graft for vascular access Forearm Including Elbow | Insertion of graft for vascular access Upper arm

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0398232
UMLS CUI [1,2]
C1140618
UMLS CUI [2,1]
C0398232
UMLS CUI [2,2]
C0016536
UMLS CUI [2,3]
C0332257
UMLS CUI [2,4]
C0013769
UMLS CUI [3,1]
C0398232
UMLS CUI [3,2]
C0446516
patient is undergoing or will undergo hemodialysis at a hospital or hemodialysis center
Beschreibung

Hemodialysis, maintenance in hospital | Hemodialysis Hemodialysis Units

Datentyp

boolean

Alias
UMLS CUI [1]
C0200022
UMLS CUI [2,1]
C0019004
UMLS CUI [2,2]
C0019007
patient has a vein 4 mm or larger to which the graft can be anastomosed
Beschreibung

Patient Has Vein Diameter | Anastomosis vascular access graft

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0030705
UMLS CUI [1,2]
C3539897
UMLS CUI [1,3]
C0042449
UMLS CUI [1,4]
C1301886
UMLS CUI [2,1]
C0002805
UMLS CUI [2,2]
C0493494
Exclusion Criteria
Beschreibung

Exclusion Criteria

Alias
UMLS CUI
C0680251
patient is unable to comply with the study follow-up
Beschreibung

Clinical Study Follow-up Compliance behavior Limited

Datentyp

boolean

Alias
UMLS CUI [1,1]
C3274571
UMLS CUI [1,2]
C1321605
UMLS CUI [1,3]
C0439801
patient has a known sensitivity to polyurethane or porcine heparin
Beschreibung

Sensitivity Polyurethanes | Sensitivity heparin, porcine

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0032616
UMLS CUI [2,1]
C0020517
UMLS CUI [2,2]
C0770546
patient has a previous vascular access graft implanted and it is not possible to place the study graft proximal to the existing device and no other sites are available
Beschreibung

Insertion of graft for vascular access Previous | Insertion of graft for vascular access Investigational Unsuccessful

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0398232
UMLS CUI [1,2]
C0205156
UMLS CUI [2,1]
C0398232
UMLS CUI [2,2]
C1517586
UMLS CUI [2,3]
C1272705
patient has an immunodeficiency syndrome
Beschreibung

Immunologic Deficiency Syndrome

Datentyp

boolean

Alias
UMLS CUI [1]
C0021051
patient has a prior history of bacterial infection within 8 weeks of implantation of graft
Beschreibung

Bacterial Infection

Datentyp

boolean

Alias
UMLS CUI [1]
C0004623
patient has a severe coagulation disorder
Beschreibung

Blood Coagulation Disorder Severe

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0005779
UMLS CUI [1,2]
C0205082
patient has an elevated platelet count of greater than 1 million
Beschreibung

Increased number of platelets

Datentyp

boolean

Alias
UMLS CUI [1]
C0857460
patient has a history of heparin-induced thrombocytopenia syndrome (hit)
Beschreibung

Heparin induced thrombocytopenia (HIT)

Datentyp

boolean

Alias
UMLS CUI [1]
C2349404
patient is pregnant
Beschreibung

Pregnancy

Datentyp

boolean

Alias
UMLS CUI [1]
C0032961
patient has a fever greater than 100 degrees fahrenheit
Beschreibung

Fever Degrees fahrenheit

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0015967
UMLS CUI [1,2]
C0456628
Zum Seitenanfang zurückkehren

Ähnliche Modelle

Eligibility End Stage Renal Disease NCT00131872

1 Formulare
Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Chronic Kidney Failure Requirement vascular access Hemodialysis
Item
patient has chronic renal failure and requires vascular access for hemodialysis
boolean
C0022661 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0750138 (UMLS CUI [1,3])
C0019004 (UMLS CUI [1,4])
Informed Consent | Protocol Compliance
Item
patient has given informed consent to participate in the trial and is willing to comply with the study protocol
boolean
C0021430 (UMLS CUI [1])
C0525058 (UMLS CUI [2])
Age
Item
patient is male or female, 18 years of age or older
boolean
C0001779 (UMLS CUI [1])
Insertion of graft for vascular access Upper Extremity | Insertion of graft for vascular access Forearm Including Elbow | Insertion of graft for vascular access Upper arm
Item
the vascular access graft can be placed in the upper extremity (forearm, including across the elbow, or upper arm)
boolean
C0398232 (UMLS CUI [1,1])
C1140618 (UMLS CUI [1,2])
C0398232 (UMLS CUI [2,1])
C0016536 (UMLS CUI [2,2])
C0332257 (UMLS CUI [2,3])
C0013769 (UMLS CUI [2,4])
C0398232 (UMLS CUI [3,1])
C0446516 (UMLS CUI [3,2])
Hemodialysis, maintenance in hospital | Hemodialysis Hemodialysis Units
Item
patient is undergoing or will undergo hemodialysis at a hospital or hemodialysis center
boolean
C0200022 (UMLS CUI [1])
C0019004 (UMLS CUI [2,1])
C0019007 (UMLS CUI [2,2])
Patient Has Vein Diameter | Anastomosis vascular access graft
Item
patient has a vein 4 mm or larger to which the graft can be anastomosed
boolean
C0030705 (UMLS CUI [1,1])
C3539897 (UMLS CUI [1,2])
C0042449 (UMLS CUI [1,3])
C1301886 (UMLS CUI [1,4])
C0002805 (UMLS CUI [2,1])
C0493494 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Clinical Study Follow-up Compliance behavior Limited
Item
patient is unable to comply with the study follow-up
boolean
C3274571 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
C0439801 (UMLS CUI [1,3])
Sensitivity Polyurethanes | Sensitivity heparin, porcine
Item
patient has a known sensitivity to polyurethane or porcine heparin
boolean
C0020517 (UMLS CUI [1,1])
C0032616 (UMLS CUI [1,2])
C0020517 (UMLS CUI [2,1])
C0770546 (UMLS CUI [2,2])
Insertion of graft for vascular access Previous | Insertion of graft for vascular access Investigational Unsuccessful
Item
patient has a previous vascular access graft implanted and it is not possible to place the study graft proximal to the existing device and no other sites are available
boolean
C0398232 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0398232 (UMLS CUI [2,1])
C1517586 (UMLS CUI [2,2])
C1272705 (UMLS CUI [2,3])
Immunologic Deficiency Syndrome
Item
patient has an immunodeficiency syndrome
boolean
C0021051 (UMLS CUI [1])
Bacterial Infection
Item
patient has a prior history of bacterial infection within 8 weeks of implantation of graft
boolean
C0004623 (UMLS CUI [1])
Blood Coagulation Disorder Severe
Item
patient has a severe coagulation disorder
boolean
C0005779 (UMLS CUI [1,1])
C0205082 (UMLS CUI [1,2])
Increased number of platelets
Item
patient has an elevated platelet count of greater than 1 million
boolean
C0857460 (UMLS CUI [1])
Heparin induced thrombocytopenia (HIT)
Item
patient has a history of heparin-induced thrombocytopenia syndrome (hit)
boolean
C2349404 (UMLS CUI [1])
Pregnancy
Item
patient is pregnant
boolean
C0032961 (UMLS CUI [1])
Fever Degrees fahrenheit
Item
patient has a fever greater than 100 degrees fahrenheit
boolean
C0015967 (UMLS CUI [1,1])
C0456628 (UMLS CUI [1,2])
Zum Seitenanfang zurückkehren 

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