ID

12956

Beschrijving

Effectiveness of the Investigational Drug Campath-1H in Preventing Rejection of Transplanted Kidneys; ODM derived from: https://clinicaltrials.gov/show/NCT00001984

Link

https://clinicaltrials.gov/show/NCT00001984

Trefwoorden

  1. 07-01-16 07-01-16 -
Houder van rechten

CC BY-NC 3.0

Geüploaded op

7 januari 2016

DOI

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Licentie

Creative Commons BY-NC 3.0

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Eligibility Graft Rejection NCT00001984

Eligibility Graft Rejection NCT00001984

Criteria
Beschrijving

Criteria

candidates for a kidney transplant performed at the warren g. magnuson clinical center.
Beschrijving

candidates for a kidney transplant performed at the warren g. magnuson clinical center.

Datatype

boolean

Alias
UMLS CUI [1]
C0022671
willingness and legal ability to give informed consent, or permission from a legal guardian.
Beschrijving

informed consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
willingness to travel to the clinical center for protocol specific samples to be taken, or in some cases, the ability to send samples via overnight mail.
Beschrijving

willingness to travel to the clinical center for protocol specific samples to be taken, or in some cases, the ability to send samples via overnight mail.

Datatype

boolean

Alias
UMLS CUI [1]
C1321605
availability of donor tissue for testing. this could include splenic or peripheral blood lymphocytes from a cadaveric donor or a willing living donor enrolled on the clinic center living donor protocol who consents to periodic phlebotomy for peripheral blood lymphocyte isolation.
Beschrijving

availability of donor tissue

Datatype

boolean

Alias
UMLS CUI [1]
C0040300
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
immunosuppressive drug therapy at the time of or 2 months prior to enrollment. specifically, candidates must not be taking prednisone, cyclosporine, tacrolimus, azathioprine, mycophenolate mofetil, antilymphocyte agents, cyclophosphamide, methotrexate, or other agents whose therapeutic effect is immunosuppressive.
Beschrijving

immunosuppressive drug therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0021081
any condition that precludes serial follow-up.
Beschrijving

any condition that precludes serial follow-up.

Datatype

boolean

Alias
UMLS CUI [1,1]
C1321605
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
any active malignancy or any history of a hematogenous malignancy or lymphoma. patients with primary, cutaneous basal cell or squamous cell cancers may be enrolled providing the lesions are appropriately treated prior to transplant.
Beschrijving

malignancy

Datatype

boolean

Alias
UMLS CUI [1]
C0006826
significant coagulopathy or requirement for anticoagulation therapy that would contraindicate protocol allograft biopsies.
Beschrijving

coagulopathy or requirement for anticoagulation therapy

Datatype

boolean

Alias
UMLS CUI [1]
C0005779
UMLS CUI [2]
C0449867
platelet count less than 100,000/mm(3).
Beschrijving

platelet count

Datatype

boolean

Alias
UMLS CUI [1]
C0005821
hemoglobin less than 9.0 mg/dl. patients may be on erythropoietin therapy, but will not be placed on therapy solely to facilitate research sample acquisition.
Beschrijving

hemoglobin

Datatype

boolean

Alias
UMLS CUI [1]
C0019046
any known immunodeficiency syndrome.
Beschrijving

immunodeficiency syndrome

Datatype

boolean

Alias
UMLS CUI [1]
C0021051
hla identical status with a living donor.
Beschrijving

hla status

Datatype

boolean

Alias
UMLS CUI [1]
C0019721
any history of uncompensated cardiac insufficiency, major vascular disease, or symptomatic coronary artery disease.
Beschrijving

cardiovascular disease

Datatype

boolean

Alias
UMLS CUI [1]
C0007222
systemic or pulmonary edema.
Beschrijving

systemic or pulmonary edema

Datatype

boolean

Alias
UMLS CUI [1]
C0013604
inability to be effectively dialyzed.
Beschrijving

inability to be effectively dialyzed.

Datatype

boolean

Alias
UMLS CUI [1]
C0011946
chronic hypotension (sbp less than 100 mmhg).
Beschrijving

hypotension

Datatype

boolean

Alias
UMLS CUI [1]
C0020649
any condition that would likely increase the risk of protocol participation or confound the interpretation of the data.
Beschrijving

any condition that would likely increase the risk of protocol participation or confound the interpretation of the data.

Datatype

boolean

Alias
UMLS CUI [1,1]
C2348563
UMLS CUI [1,2]
C0439801
UMLS CUI [1,3]
C0009488
cmv negative status receiving an organ from a known cmv positive donor.
Beschrijving

cmv status

Datatype

boolean

Alias
UMLS CUI [1]
C0010825
ebv negative status receiving an organ from a known ebv positive donor.
Beschrijving

ebv status

Datatype

boolean

Alias
UMLS CUI [1]
C0014644
panel reactive antibody greater than 20% due to hla antibodies.
Beschrijving

panel reactive antibody

Datatype

boolean

Alias
UMLS CUI [1]
C1141951

Similar models

Eligibility Graft Rejection NCT00001984

Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
candidates for a kidney transplant performed at the warren g. magnuson clinical center.
Item
candidates for a kidney transplant performed at the warren g. magnuson clinical center.
boolean
C0022671 (UMLS CUI [1])
informed consent
Item
willingness and legal ability to give informed consent, or permission from a legal guardian.
boolean
C0021430 (UMLS CUI [1])
willingness to travel to the clinical center for protocol specific samples to be taken, or in some cases, the ability to send samples via overnight mail.
Item
willingness to travel to the clinical center for protocol specific samples to be taken, or in some cases, the ability to send samples via overnight mail.
boolean
C1321605 (UMLS CUI [1])
availability of donor tissue
Item
availability of donor tissue for testing. this could include splenic or peripheral blood lymphocytes from a cadaveric donor or a willing living donor enrolled on the clinic center living donor protocol who consents to periodic phlebotomy for peripheral blood lymphocyte isolation.
boolean
C0040300 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
immunosuppressive drug therapy
Item
immunosuppressive drug therapy at the time of or 2 months prior to enrollment. specifically, candidates must not be taking prednisone, cyclosporine, tacrolimus, azathioprine, mycophenolate mofetil, antilymphocyte agents, cyclophosphamide, methotrexate, or other agents whose therapeutic effect is immunosuppressive.
boolean
C0021081 (UMLS CUI [1])
any condition that precludes serial follow-up.
Item
any condition that precludes serial follow-up.
boolean
C1321605 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
malignancy
Item
any active malignancy or any history of a hematogenous malignancy or lymphoma. patients with primary, cutaneous basal cell or squamous cell cancers may be enrolled providing the lesions are appropriately treated prior to transplant.
boolean
C0006826 (UMLS CUI [1])
coagulopathy or requirement for anticoagulation therapy
Item
significant coagulopathy or requirement for anticoagulation therapy that would contraindicate protocol allograft biopsies.
boolean
C0005779 (UMLS CUI [1])
C0449867 (UMLS CUI [2])
platelet count
Item
platelet count less than 100,000/mm(3).
boolean
C0005821 (UMLS CUI [1])
hemoglobin
Item
hemoglobin less than 9.0 mg/dl. patients may be on erythropoietin therapy, but will not be placed on therapy solely to facilitate research sample acquisition.
boolean
C0019046 (UMLS CUI [1])
immunodeficiency syndrome
Item
any known immunodeficiency syndrome.
boolean
C0021051 (UMLS CUI [1])
hla status
Item
hla identical status with a living donor.
boolean
C0019721 (UMLS CUI [1])
cardiovascular disease
Item
any history of uncompensated cardiac insufficiency, major vascular disease, or symptomatic coronary artery disease.
boolean
C0007222 (UMLS CUI [1])
systemic or pulmonary edema
Item
systemic or pulmonary edema.
boolean
C0013604 (UMLS CUI [1])
inability to be effectively dialyzed.
Item
inability to be effectively dialyzed.
boolean
C0011946 (UMLS CUI [1])
hypotension
Item
chronic hypotension (sbp less than 100 mmhg).
boolean
C0020649 (UMLS CUI [1])
any condition that would likely increase the risk of protocol participation or confound the interpretation of the data.
Item
any condition that would likely increase the risk of protocol participation or confound the interpretation of the data.
boolean
C2348563 (UMLS CUI [1,1])
C0439801 (UMLS CUI [1,2])
C0009488 (UMLS CUI [1,3])
cmv status
Item
cmv negative status receiving an organ from a known cmv positive donor.
boolean
C0010825 (UMLS CUI [1])
ebv status
Item
ebv negative status receiving an organ from a known ebv positive donor.
boolean
C0014644 (UMLS CUI [1])
panel reactive antibody
Item
panel reactive antibody greater than 20% due to hla antibodies.
boolean
C1141951 (UMLS CUI [1])

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