ID

29292

Description

DIVINE: Dialysis Infection and Vitamin D In New England; ODM derived from: https://clinicaltrials.gov/show/NCT00892099

Link

https://clinicaltrials.gov/show/NCT00892099

Keywords

Versions (1)
  1. 3/16/18 3/16/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

March 16, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility End Stage Renal Disease NCT00892099

English

Eligibility End Stage Renal Disease NCT00892099

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
age ≥ 18 years
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
initiating chronic hemodialysis 3x/wk at massachusetts general hospital, brigham and women's hospital or beth israel deaconess medical center with planned transfer to massachusetts chronic facility
Description

Initiation Chronic haemodialysis Frequency

Data type

boolean

Alias
UMLS CUI [1,1]
C1704686
UMLS CUI [1,2]
C1740835
UMLS CUI [1,3]
C0439603
serum 25d < 32 ng/ml
Description

serum 25-hydroxyvitamin D measurement

Data type

boolean

Alias
UMLS CUI [1]
C2229552
corrected serum calcium < 10.2 mg/dl
Description

Corrected serum calcium measurement

Data type

boolean

Alias
UMLS CUI [1]
C0455288
serum phosphate < 5.5 mg/dl
Description

Serum Phosphate Measurement

Data type

boolean

Alias
UMLS CUI [1]
C1883013
serum albumin > 3 g/dl
Description

Serum albumin measurement

Data type

boolean

Alias
UMLS CUI [1]
C0523465
informed consent
Description

Informed Consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
pregnant or breastfeeding
Description

Pregnancy | Breast Feeding

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
women of childbearing potential not practicing one of the following measures of birth control: double-barrier method, hormonal contraceptives for at least 3 months prior to and during study, monogamous relationship with vasectomized partner, total abstinence from sexual intercourse with men during study.
Description

Childbearing Potential Contraceptive methods Absent | Barrier Contraception Double | Hormonal contraception | In monogamous relationship Partner had vasectomy | Sexual Abstinence

Data type

boolean

Alias
UMLS CUI [1,1]
C3831118
UMLS CUI [1,2]
C0700589
UMLS CUI [1,3]
C0332197
UMLS CUI [2,1]
C0004764
UMLS CUI [2,2]
C0205173
UMLS CUI [3]
C2985296
UMLS CUI [4,1]
C2135319
UMLS CUI [4,2]
C0420842
UMLS CUI [5]
C0036899
hiv positive
Description

HIV Seropositivity

Data type

boolean

Alias
UMLS CUI [1]
C0019699
history of allergic reaction to ergocalciferol
Description

Allergic Reaction Ergocalciferol

Data type

boolean

Alias
UMLS CUI [1,1]
C1527304
UMLS CUI [1,2]
C0014695
investigator considers subject unsuitable for any reason
Description

Study Subject Participation Status Inappropriate

Data type

boolean

Alias
UMLS CUI [1,1]
C2348568
UMLS CUI [1,2]
C1548788
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Similar models

Eligibility End Stage Renal Disease NCT00892099

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Age
Item
age ≥ 18 years
boolean
C0001779 (UMLS CUI [1])
Initiation Chronic haemodialysis Frequency
Item
initiating chronic hemodialysis 3x/wk at massachusetts general hospital, brigham and women's hospital or beth israel deaconess medical center with planned transfer to massachusetts chronic facility
boolean
C1704686 (UMLS CUI [1,1])
C1740835 (UMLS CUI [1,2])
C0439603 (UMLS CUI [1,3])
serum 25-hydroxyvitamin D measurement
Item
serum 25d < 32 ng/ml
boolean
C2229552 (UMLS CUI [1])
Corrected serum calcium measurement
Item
corrected serum calcium < 10.2 mg/dl
boolean
C0455288 (UMLS CUI [1])
Serum Phosphate Measurement
Item
serum phosphate < 5.5 mg/dl
boolean
C1883013 (UMLS CUI [1])
Serum albumin measurement
Item
serum albumin > 3 g/dl
boolean
C0523465 (UMLS CUI [1])
Informed Consent
Item
informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Pregnancy | Breast Feeding
Item
pregnant or breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Childbearing Potential Contraceptive methods Absent | Barrier Contraception Double | Hormonal contraception | In monogamous relationship Partner had vasectomy | Sexual Abstinence
Item
women of childbearing potential not practicing one of the following measures of birth control: double-barrier method, hormonal contraceptives for at least 3 months prior to and during study, monogamous relationship with vasectomized partner, total abstinence from sexual intercourse with men during study.
boolean
C3831118 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
C0332197 (UMLS CUI [1,3])
C0004764 (UMLS CUI [2,1])
C0205173 (UMLS CUI [2,2])
C2985296 (UMLS CUI [3])
C2135319 (UMLS CUI [4,1])
C0420842 (UMLS CUI [4,2])
C0036899 (UMLS CUI [5])
HIV Seropositivity
Item
hiv positive
boolean
C0019699 (UMLS CUI [1])
Allergic Reaction Ergocalciferol
Item
history of allergic reaction to ergocalciferol
boolean
C1527304 (UMLS CUI [1,1])
C0014695 (UMLS CUI [1,2])
Study Subject Participation Status Inappropriate
Item
investigator considers subject unsuitable for any reason
boolean
C2348568 (UMLS CUI [1,1])
C1548788 (UMLS CUI [1,2])
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