ID

15074

Description

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

Link

https://clinicaltrials.gov/show/NCT02240381

Keywords

Versions (1)
  1. 5/14/16 5/14/16 -
Uploaded on

May 14, 2016

DOI

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License

Creative Commons BY 4.0
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Eligibility Diabetes Mellitus NCT02240381

English

Eligibility Diabetes Mellitus NCT02240381

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
patients undergoing mrd allogeneic hct
Description

Neoplasm, Residual | Allogeneic Hematopoietic Stem Cell Transplantation

Data type

boolean

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

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

Data type

boolean

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

Exclusion Criteria

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

Allogeneic Hematopoietic Stem Cell Transplantation

Data type

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
Description

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

Data type

boolean

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

Pregnancy | Breast Feeding

Data type

boolean

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

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

Data type

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
Description

T-cell depletion | Thymoglobulin | Cell Transplants

Data type

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
Description

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

Data type

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
Description

Unable Informed Consent

Data type

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
Description

Condition Interferes with Study Protocol

Data type

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
Description

Indication of Risk Patient

Data type

boolean

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

Stem cell donor | Study Subject donating stem cells

Data type

boolean

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

Stem cell donor | Pregnancy | Breast Feeding

Data type

boolean

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

Stem cell donor | Unable Informed Consent

Data type

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
Description

Stem cell donor | Condition Interferes with Study Protocol

Data type

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 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
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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