ID

15074

Descrizione

Predicting Development of Diabetes Mellitus in Patients Undergoing Allogeneic Stem Cell Transplant; ODM derived from: https://clinicaltrials.gov/show/NCT02240381

collegamento

https://clinicaltrials.gov/show/NCT02240381

Keywords

versioni (1)
  1. 14/05/16 14/05/16 -
Caricato su

14 maggio 2016

DOI

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Licenza

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus NCT02240381

Inglese

Eligibility Diabetes Mellitus NCT02240381

1 moduli  
Inclusion Criteria
Descrizione

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing mrd allogeneic hct
Descrizione

Neoplasm, Residual | Allogeneic Hematopoietic Stem Cell Transplantation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0242596
UMLS CUI [2]
C1705576
donor: donors undergoing stem cell collection for match related allogeneic stem cell transplant
Descrizione

Stem cell donor | Stem Cell Isolation Allogenic hematopoietic stem cell transplant

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0375877
UMLS CUI [2,1]
C3827940
UMLS CUI [2,2]
C1456094
Exclusion Criteria
Descrizione

Exclusion Criteria

Alias
UMLS CUI
C0680251
patients who have not received an allogeneic hct
Descrizione

Allogeneic Hematopoietic Stem Cell Transplantation

Tipo di dati

boolean

Alias
UMLS CUI [1]
C1705576
recent or current history of diabetes mellitus, defined as:1) diabetes therapy within 6 months of enrollment, or 2) fasting blood glucose at "pre-admit" (screening) visit >= 126 mg/dl
Descrizione

H/O: diabetes mellitus | Diabetes mellitus management | Fasting blood glucose measurement

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0455488
UMLS CUI [2]
C0948092
UMLS CUI [3]
C0428568
pregnancy or breastfeeding
Descrizione

Pregnancy | Breast Feeding

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
unrelated donor, umbilical cord blood, mismatched, or haploidentical transplants
Descrizione

Unrelated Donors | Umbilical Cord Blood | Mismatch | Cell Transplants Haploidentical

Tipo di dati

boolean

Alias
UMLS CUI [1]
C3179133
UMLS CUI [2]
C0162371
UMLS CUI [3]
C1881865
UMLS CUI [4,1]
C0206152
UMLS CUI [4,2]
C3829897
patients receiving t cell depletion or thymoglobulin as part of their transplant
Descrizione

T-cell depletion | Thymoglobulin | Cell Transplants

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0677960
UMLS CUI [2]
C0730920
UMLS CUI [3]
C0206152
patients on established, chronic corticosteroid therapy (> 5 mg /day of prednisone or prednisone equivalent) prior to transplant; established, chronic corticosteroid therapy is defined as daily dosing of > 5 mg/day of prednisone or prednisone equivalent for at least 2 weeks prior to the start of conditioning/chemotherapy or plans to continue pre-transplant corticosteroids (> 5 mg/day of prednisone or prednisone equivalent) indefinitely after transplantation
Descrizione

Steroid therapy | Prednisone | Transplantation | Transplantation Conditioning | Chemotherapy Regimen

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0149783
UMLS CUI [2]
C0032952
UMLS CUI [3]
C0040732
UMLS CUI [4]
C0376450
UMLS CUI [5]
C0392920
inability to give informed consent
Descrizione

Unable Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C1299582
UMLS CUI [1,2]
C0021430
any condition which, in the opinion of the investigator, might interfere with study objective
Descrizione

Condition Interferes with Study Protocol

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C2348563
any reason which, in the opinion of the investigator, adds additional risk to the patient
Descrizione

Indication of Risk Patient

Tipo di dati

boolean

Alias
UMLS CUI [1,1]
C0392360
UMLS CUI [1,2]
C0035647
UMLS CUI [1,3]
C0030705
donor: individuals not donating stem cells
Descrizione

Stem cell donor | Study Subject donating stem cells

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0375877
UMLS CUI [2,1]
C0681850
UMLS CUI [2,2]
C2145402
donor: pregnancy or breastfeeding
Descrizione

Stem cell donor | Pregnancy | Breast Feeding

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0375877
UMLS CUI [2]
C0032961
UMLS CUI [3]
C0006147
donor: inability to give informed consent
Descrizione

Stem cell donor | Unable Informed Consent

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0375877
UMLS CUI [2,1]
C1299582
UMLS CUI [2,2]
C0021430
donor: any condition which, in the opinion of the investigator, might interfere with study objective
Descrizione

Stem cell donor | Condition Interferes with Study Protocol

Tipo di dati

boolean

Alias
UMLS CUI [1]
C0375877
UMLS CUI [2,1]
C0348080
UMLS CUI [2,2]
C0521102
UMLS CUI [2,3]
C2348563
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Similar models

Eligibility Diabetes Mellitus NCT02240381

1 moduli
Name
genere
Description | Question | Decode (Coded Value)
Tipo di dati
Alias
Item Group
C1512693 (UMLS CUI)
Neoplasm, Residual | Allogeneic Hematopoietic Stem Cell Transplantation
Item
patients undergoing mrd allogeneic hct
boolean
C0242596 (UMLS CUI [1])
C1705576 (UMLS CUI [2])
Stem cell donor | Stem Cell Isolation Allogenic hematopoietic stem cell transplant
Item
donor: donors undergoing stem cell collection for match related allogeneic stem cell transplant
boolean
C0375877 (UMLS CUI [1])
C3827940 (UMLS CUI [2,1])
C1456094 (UMLS CUI [2,2])
Item Group
C0680251 (UMLS CUI)
Allogeneic Hematopoietic Stem Cell Transplantation
Item
patients who have not received an allogeneic hct
boolean
C1705576 (UMLS CUI [1])
H/O: diabetes mellitus | Diabetes mellitus management | Fasting blood glucose measurement
Item
recent or current history of diabetes mellitus, defined as:1) diabetes therapy within 6 months of enrollment, or 2) fasting blood glucose at "pre-admit" (screening) visit >= 126 mg/dl
boolean
C0455488 (UMLS CUI [1])
C0948092 (UMLS CUI [2])
C0428568 (UMLS CUI [3])
Pregnancy | Breast Feeding
Item
pregnancy or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Unrelated Donors | Umbilical Cord Blood | Mismatch | Cell Transplants Haploidentical
Item
unrelated donor, umbilical cord blood, mismatched, or haploidentical transplants
boolean
C3179133 (UMLS CUI [1])
C0162371 (UMLS CUI [2])
C1881865 (UMLS CUI [3])
C0206152 (UMLS CUI [4,1])
C3829897 (UMLS CUI [4,2])
T-cell depletion | Thymoglobulin | Cell Transplants
Item
patients receiving t cell depletion or thymoglobulin as part of their transplant
boolean
C0677960 (UMLS CUI [1])
C0730920 (UMLS CUI [2])
C0206152 (UMLS CUI [3])
Steroid therapy | Prednisone | Transplantation | Transplantation Conditioning | Chemotherapy Regimen
Item
patients on established, chronic corticosteroid therapy (> 5 mg /day of prednisone or prednisone equivalent) prior to transplant; established, chronic corticosteroid therapy is defined as daily dosing of > 5 mg/day of prednisone or prednisone equivalent for at least 2 weeks prior to the start of conditioning/chemotherapy or plans to continue pre-transplant corticosteroids (> 5 mg/day of prednisone or prednisone equivalent) indefinitely after transplantation
boolean
C0149783 (UMLS CUI [1])
C0032952 (UMLS CUI [2])
C0040732 (UMLS CUI [3])
C0376450 (UMLS CUI [4])
C0392920 (UMLS CUI [5])
Unable Informed Consent
Item
inability to give informed consent
boolean
C1299582 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
Condition Interferes with Study Protocol
Item
any condition which, in the opinion of the investigator, might interfere with study objective
boolean
C0348080 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C2348563 (UMLS CUI [1,3])
Indication of Risk Patient
Item
any reason which, in the opinion of the investigator, adds additional risk to the patient
boolean
C0392360 (UMLS CUI [1,1])
C0035647 (UMLS CUI [1,2])
C0030705 (UMLS CUI [1,3])
Stem cell donor | Study Subject donating stem cells
Item
donor: individuals not donating stem cells
boolean
C0375877 (UMLS CUI [1])
C0681850 (UMLS CUI [2,1])
C2145402 (UMLS CUI [2,2])
Stem cell donor | Pregnancy | Breast Feeding
Item
donor: pregnancy or breastfeeding
boolean
C0375877 (UMLS CUI [1])
C0032961 (UMLS CUI [2])
C0006147 (UMLS CUI [3])
Stem cell donor | Unable Informed Consent
Item
donor: inability to give informed consent
boolean
C0375877 (UMLS CUI [1])
C1299582 (UMLS CUI [2,1])
C0021430 (UMLS CUI [2,2])
Stem cell donor | Condition Interferes with Study Protocol
Item
donor: any condition which, in the opinion of the investigator, might interfere with study objective
boolean
C0375877 (UMLS CUI [1])
C0348080 (UMLS CUI [2,1])
C0521102 (UMLS CUI [2,2])
C2348563 (UMLS CUI [2,3])
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