ID

44483

Description

Caloric Restriction in Treating Patients With Stage 0-I Breast Cancer Undergoing Surgery and Radiation Therapy; ODM derived from: https://clinicaltrials.gov/show/NCT01819233

Link

https://clinicaltrials.gov/show/NCT01819233

Keywords

Versions (2)
  1. 1/20/18 1/20/18 -
  2. 9/27/21 9/27/21 -
Copyright Holder

https://clinicaltrials.gov/show/NCT01819233

Uploaded on

September 27, 2021

DOI

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License

Creative Commons BY 4.0
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Eligibility Ductal Breast Carcinoma in Situ NCT01819233

English

Eligibility Ductal Breast Carcinoma in Situ NCT01819233

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
1. pathologically proven diagnosis of ductal carcinoma in situ (dcis) or invasive breast cancer
Description

breast cancer or ductal carcinoma in situ

Data type

boolean

Alias
UMLS CUI [1]
C0007124
UMLS CUI [2]
C0678222
2. ability to have breast conservation as determined by the judgment of the radiation oncologist, for which the radiation oncologist has determined that he or she will only treat the whole breast and not regional lymph nodes
Description

breast cancer conservation therapy

Data type

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2]
C0917927
3. the patient must be female
Description

gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
4. age >= 18
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
5. if multifocal breast cancer, then it must be able to be resected through a single lumpectomy incision
Description

multifocal breast cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205292
UMLS CUI [2]
C0024885
6. appropriate stage for protocol entry, including no clinical evidence for distant metastases, based upon the following minimum diagnostic workup:
Description

breast cancer stage and metastases

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C1300072
UMLS CUI [2]
C0027627
1. history/physical examination, including breast exam and documentation of weight and karnofsky performance status of 80-100 for at least 60 days prior to study entry
Description

physical examination with breast exam, weight and karnofsky performance status

Data type

boolean

Alias
UMLS CUI [1,1]
C0031809
UMLS CUI [1,2]
C2347781
UMLS CUI [1,3]
C0005910
UMLS CUI [2]
C0206065
2. ipsilateral mammogram within 6 months prior to study entry
Description

mammography

Data type

boolean

Alias
UMLS CUI [1]
C0024671
7. women of childbearing potential must have a negative serum pregnancy test within 14 days of study entry
Description

pregnancy

Data type

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0205160
8. women of childbearing potential must be non-pregnant and non-lactating and willing to use medically acceptable form of contraception during radiation therapy
Description

pregnancy, breastfeeding and contraception

Data type

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
UMLS CUI [3]
C0700589
9. patient must capable of and provide study specific informed consent prior to study entry
Description

informed consent

Data type

boolean

Alias
UMLS CUI [1]
C0021430
10. body mass index (bmi) >= 21
Description

body mass index

Data type

boolean

Alias
UMLS CUI [1]
C1305855
11. weight >= 100 lbs
Description

weight

Data type

boolean

Alias
UMLS CUI [1]
C0005910
12. no prior history of non-breast malignancies in the past 2 years unless it was a non-melanomatous skin lesion or carcinoma in situ of the cervix
Description

cancer history

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0006826
13. patient must not have any of the following severe, active co-morbidity, defined as follows:
Description

comorbidities

Data type

boolean

Alias
UMLS CUI [1]
C0009488
1. unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months
Description

unstable angina and/or congestive heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0002965
2. transmural myocardial infarction within the last 6 months
Description

myocardial infarction

Data type

boolean

Alias
UMLS CUI [1]
C0027051
3. acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
Description

current infection therapy, antibiotics

Data type

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0003232
4. chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days before registration
Description

respiratory illness

Data type

boolean

Alias
UMLS CUI [1]
C0035204
UMLS CUI [2]
C0024117
5. hepatic insufficiency resulting in clinical jaundice and/or coagulation defects; note, however, that laboratory tests for liver function and coagulation parameters are not required for entry into this protocol
Description

hepatic insufficiency

Data type

boolean

Alias
UMLS CUI [1]
C1306571
6. acquired immune deficiency syndrome (aids) or human immunodeficiency virus (hiv) positive based upon current centers for disease and control (cdc) definition; note, however, that hiv testing is not required for entry into this protocol; the need to exclude patients with aids or hiv from this protocol is necessary because anti-retrovirals may alter patient metabolism
Description

HIV or AIDS

Data type

boolean

Alias
UMLS CUI [1,1]
C0019699
UMLS CUI [1,2]
C0001175
14. patient must not have active systemic lupus, erythematosus, or any history of scleroderma, dermatomyositis with active rash
Description

skin diseases

Data type

boolean

Alias
UMLS CUI [1,1]
C1123023
UMLS CUI [1,2]
C0012634
15. no prior radiotherapy to the ipsilateral breast or prior radiation to the region of the breast that would result in overlap of radiation therapy fields
Description

prior breast cancer therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0087111
16. patient may not have any active gastrointestinal/malabsorption disorder at the discretion of the principal investigator
Description

gastrointestinal disorder

Data type

boolean

Alias
UMLS CUI [1]
C0017178
1. inflammatory bowel disease
Description

inflammatory bowel disease

Data type

boolean

Alias
UMLS CUI [1]
C0021390
2. celiac disease
Description

celiac disease

Data type

boolean

Alias
UMLS CUI [1]
C0007570
3. chronic pancreatitis
Description

chronic pancreatitis

Data type

boolean

Alias
UMLS CUI [1]
C0030305
4. chronic diarrhea or vomiting
Description

chronic diarrhea or vomiting

Data type

boolean

Alias
UMLS CUI [1]
C0042963
UMLS CUI [2]
C0011991
5. active eating disorder
Description

eating disorder

Data type

boolean

Alias
UMLS CUI [1]
C0013473
17. creatinine < 1.7
Description

creatinine

Data type

boolean

Alias
UMLS CUI [1]
C0201976
18. not currently taking steroids
Description

steriods

Data type

boolean

Alias
UMLS CUI [1]
C0038317
19. no currently active pituitary secreting tumors up to physician discretion
Description

pituitary tumor

Data type

boolean

Alias
UMLS CUI [1,1]
C0032005
UMLS CUI [1,2]
C0006826
20. no history of or current active drug/alcohol dependence
Description

drug/alcohol dependence

Data type

boolean

Alias
UMLS CUI [1]
C0038580
UMLS CUI [2]
C0085762
21. no patients being decisionally impaired
Description

informed consent not possible

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
1. patient is not a candidate for breast conservation
Description

breast conservation not possible

Data type

boolean

Alias
UMLS CUI [1,1]
C0917927
UMLS CUI [1,2]
C1518422
UMLS CUI [1,3]
C0332149
2. patient is male
Description

gender

Data type

boolean

Alias
UMLS CUI [1]
C0079399
3. age < 18 years
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
4. patient requires regional lymph node irradiation therapy
Description

lymph node metastases

Data type

boolean

Alias
UMLS CUI [1,1]
C0024204
UMLS CUI [1,2]
C0027627
5. patient has evidence of distant metastases
Description

metastases

Data type

boolean

Alias
UMLS CUI [1]
C0027627
6. karnofsky performance status less than 80% within 60 days prior to study
Description

karnofsky performance status

Data type

boolean

Alias
UMLS CUI [1]
C0206065
7. ipsilateral mammogram done greater than 6 months prior to study
Description

mammography

Data type

boolean

Alias
UMLS CUI [1]
C0024671
8. women of childbearing potential with a positive serum beta human chorionic gonadotropin (hcg)
Description

pregnancy, hcg positive

Data type

boolean

Alias
UMLS CUI [1]
C0032961
9. patient has a history of dementia, psychosis or other disorder affecting their mental status to the point where they cannot consent or comply with study guidelines
Description

compliance and mental disorders

Data type

boolean

Alias
UMLS CUI [1,1]
C0004936
UMLS CUI [1,2]
C1321605
10. bmi < 21
Description

BMI

Data type

boolean

Alias
UMLS CUI [1]
C1305855
11. weight < 100 lbs
Description

weight

Data type

boolean

Alias
UMLS CUI [1]
C0005910
12. weight loss >= 10% in the last 3 months (mos)
Description

weight loss

Data type

boolean

Alias
UMLS CUI [1]
C1262477
13. prior invasive non-breast malignancy (except non-melanomatous skin cancer, carcinoma in situ of the cervix) unless disease free for a minimum of 2 years prior to registration
Description

cancer history

Data type

boolean

Alias
UMLS CUI [1,1]
C0262926
UMLS CUI [1,2]
C0006826
14. two or more breast cancers not resectable through a single lumpectomy incision
Description

multifocal breast cancer

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0205292
UMLS CUI [2]
C0024885
15. non-epithelial breast malignancies such as sarcoma or lymphoma
Description

sarcoma or lymphoma

Data type

boolean

Alias
UMLS CUI [1]
C1261473
UMLS CUI [2]
C0024299
16. prior radiotherapy to the ipsilateral breast or prior radiation to the region of the breast that would result in overlap of radiation therapy fields
Description

prior breast cancer therapy

Data type

boolean

Alias
UMLS CUI [1,1]
C0678222
UMLS CUI [1,2]
C0087111
17. severe, active co-morbidity, defined as follows:
Description

comorbidities

Data type

boolean

Alias
UMLS CUI [1]
C0009488
1. unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months
Description

unstable angina and/or congestive heart failure

Data type

boolean

Alias
UMLS CUI [1]
C0018802
UMLS CUI [2]
C0002965
2. transmural myocardial infarction within the last 6 months
Description

myocardial infarction

Data type

boolean

Alias
UMLS CUI [1]
C0027051
3. acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
Description

current infection therapy, antibiotics

Data type

boolean

Alias
UMLS CUI [1]
C0009450
UMLS CUI [2]
C0003232
4. chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days before registration
Description

respiratory illness

Data type

boolean

Alias
UMLS CUI [1]
C0035204
UMLS CUI [2]
C0024117
5. hepatic insufficiency resulting in clinical jaundice and/or coagulation defects; note, however, that laboratory tests for liver function and coagulation parameters are not required for entry into this protocol
Description

hepatic insufficiency

Data type

boolean

Alias
UMLS CUI [1]
C1306571
6. acquired immune deficiency syndrome (aids) or hiv positive based upon current cdc definition; note, however, that hiv testing is not required for entry into this protocol; the need to exclude patients with aids or hiv from this protocol is necessary because anti-retrovirals may alter patient metabolism
Description

HIV or AIDS

Data type

boolean

Alias
UMLS CUI [1,1]
C0019699
UMLS CUI [1,2]
C0001175
18. active systemic lupus, erythematosus, or any history of scleroderma, dermatomyositis with active rash
Description

skin diseases

Data type

boolean

Alias
UMLS CUI [1,1]
C1123023
UMLS CUI [1,2]
C0012634
19. active gastrointestinal/malabsorption disorder at the discretion of the principal investigator
Description

gastrointestinal disorder

Data type

boolean

Alias
UMLS CUI [1]
C0017178
1. inflammatory bowel disease
Description

inflammatory bowel disease

Data type

boolean

Alias
UMLS CUI [1]
C0021390
2. celiac disease
Description

celiac disease

Data type

boolean

Alias
UMLS CUI [1]
C0007570
3. chronic pancreatitis
Description

chronic pancreatitis

Data type

boolean

Alias
UMLS CUI [1]
C0030305
4. chronic diarrhea or vomiting
Description

chronic diarrhea or vomiting

Data type

boolean

Alias
UMLS CUI [1]
C0042963
UMLS CUI [2]
C0011991
5. active eating disorder
Description

eating disorders

Data type

boolean

Alias
UMLS CUI [1]
C0013473
20. creatinine >= 1.7
Description

creatinine

Data type

boolean

Alias
UMLS CUI [1]
C0201976
21. current use of steroids
Description

use of steroids

Data type

boolean

Alias
UMLS CUI [1]
C0038317
22. pituitary secreting tumors up to physician discretion
Description

pituitary tumors

Data type

boolean

Alias
UMLS CUI [1,1]
C0032005
UMLS CUI [1,2]
C0006826
23. active drug/alcohol dependence or abuse history
Description

drug/alcohol dependence

Data type

boolean

Alias
UMLS CUI [1]
C0038580
UMLS CUI [2]
C0085762
24. decisionally impaired patients
Description

informed consent not possible

Data type

boolean

Alias
UMLS CUI [1,1]
C0021430
UMLS CUI [1,2]
C1299582
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Similar models

Eligibility Ductal Breast Carcinoma in Situ NCT01819233

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
breast cancer or ductal carcinoma in situ
Item
1. pathologically proven diagnosis of ductal carcinoma in situ (dcis) or invasive breast cancer
boolean
C0007124 (UMLS CUI [1])
C0678222 (UMLS CUI [2])
breast cancer conservation therapy
Item
2. ability to have breast conservation as determined by the judgment of the radiation oncologist, for which the radiation oncologist has determined that he or she will only treat the whole breast and not regional lymph nodes
boolean
C0678222 (UMLS CUI [1])
C0917927 (UMLS CUI [2])
gender
Item
3. the patient must be female
boolean
C0079399 (UMLS CUI [1])
age
Item
4. age >= 18
boolean
C0001779 (UMLS CUI [1])
multifocal breast cancer
Item
5. if multifocal breast cancer, then it must be able to be resected through a single lumpectomy incision
boolean
C0678222 (UMLS CUI [1,1])
C0205292 (UMLS CUI [1,2])
C0024885 (UMLS CUI [2])
breast cancer stage and metastases
Item
6. appropriate stage for protocol entry, including no clinical evidence for distant metastases, based upon the following minimum diagnostic workup:
boolean
C0678222 (UMLS CUI [1,1])
C1300072 (UMLS CUI [1,2])
C0027627 (UMLS CUI [2])
physical examination with breast exam, weight and karnofsky performance status
Item
1. history/physical examination, including breast exam and documentation of weight and karnofsky performance status of 80-100 for at least 60 days prior to study entry
boolean
C0031809 (UMLS CUI [1,1])
C2347781 (UMLS CUI [1,2])
C0005910 (UMLS CUI [1,3])
C0206065 (UMLS CUI [2])
mammography
Item
2. ipsilateral mammogram within 6 months prior to study entry
boolean
C0024671 (UMLS CUI [1])
pregnancy
Item
7. women of childbearing potential must have a negative serum pregnancy test within 14 days of study entry
boolean
C0032961 (UMLS CUI [1,1])
C0205160 (UMLS CUI [1,2])
pregnancy, breastfeeding and contraception
Item
8. women of childbearing potential must be non-pregnant and non-lactating and willing to use medically acceptable form of contraception during radiation therapy
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0700589 (UMLS CUI [3])
informed consent
Item
9. patient must capable of and provide study specific informed consent prior to study entry
boolean
C0021430 (UMLS CUI [1])
body mass index
Item
10. body mass index (bmi) >= 21
boolean
C1305855 (UMLS CUI [1])
weight
Item
11. weight >= 100 lbs
boolean
C0005910 (UMLS CUI [1])
cancer history
Item
12. no prior history of non-breast malignancies in the past 2 years unless it was a non-melanomatous skin lesion or carcinoma in situ of the cervix
boolean
C0262926 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
comorbidities
Item
13. patient must not have any of the following severe, active co-morbidity, defined as follows:
boolean
C0009488 (UMLS CUI [1])
unstable angina and/or congestive heart failure
Item
1. unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months
boolean
C0018802 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
myocardial infarction
Item
2. transmural myocardial infarction within the last 6 months
boolean
C0027051 (UMLS CUI [1])
current infection therapy, antibiotics
Item
3. acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
boolean
C0009450 (UMLS CUI [1])
C0003232 (UMLS CUI [2])
respiratory illness
Item
4. chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days before registration
boolean
C0035204 (UMLS CUI [1])
C0024117 (UMLS CUI [2])
hepatic insufficiency
Item
5. hepatic insufficiency resulting in clinical jaundice and/or coagulation defects; note, however, that laboratory tests for liver function and coagulation parameters are not required for entry into this protocol
boolean
C1306571 (UMLS CUI [1])
HIV or AIDS
Item
6. acquired immune deficiency syndrome (aids) or human immunodeficiency virus (hiv) positive based upon current centers for disease and control (cdc) definition; note, however, that hiv testing is not required for entry into this protocol; the need to exclude patients with aids or hiv from this protocol is necessary because anti-retrovirals may alter patient metabolism
boolean
C0019699 (UMLS CUI [1,1])
C0001175 (UMLS CUI [1,2])
skin diseases
Item
14. patient must not have active systemic lupus, erythematosus, or any history of scleroderma, dermatomyositis with active rash
boolean
C1123023 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
prior breast cancer therapy
Item
15. no prior radiotherapy to the ipsilateral breast or prior radiation to the region of the breast that would result in overlap of radiation therapy fields
boolean
C0678222 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
gastrointestinal disorder
Item
16. patient may not have any active gastrointestinal/malabsorption disorder at the discretion of the principal investigator
boolean
C0017178 (UMLS CUI [1])
inflammatory bowel disease
Item
1. inflammatory bowel disease
boolean
C0021390 (UMLS CUI [1])
celiac disease
Item
2. celiac disease
boolean
C0007570 (UMLS CUI [1])
chronic pancreatitis
Item
3. chronic pancreatitis
boolean
C0030305 (UMLS CUI [1])
chronic diarrhea or vomiting
Item
4. chronic diarrhea or vomiting
boolean
C0042963 (UMLS CUI [1])
C0011991 (UMLS CUI [2])
eating disorder
Item
5. active eating disorder
boolean
C0013473 (UMLS CUI [1])
creatinine
Item
17. creatinine < 1.7
boolean
C0201976 (UMLS CUI [1])
steriods
Item
18. not currently taking steroids
boolean
C0038317 (UMLS CUI [1])
pituitary tumor
Item
19. no currently active pituitary secreting tumors up to physician discretion
boolean
C0032005 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
drug/alcohol dependence
Item
20. no history of or current active drug/alcohol dependence
boolean
C0038580 (UMLS CUI [1])
C0085762 (UMLS CUI [2])
informed consent not possible
Item
21. no patients being decisionally impaired
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
Item Group
C0680251 (UMLS CUI)
breast conservation not possible
Item
1. patient is not a candidate for breast conservation
boolean
C0917927 (UMLS CUI [1,1])
C1518422 (UMLS CUI [1,2])
C0332149 (UMLS CUI [1,3])
gender
Item
2. patient is male
boolean
C0079399 (UMLS CUI [1])
age
Item
3. age < 18 years
boolean
C0001779 (UMLS CUI [1])
lymph node metastases
Item
4. patient requires regional lymph node irradiation therapy
boolean
C0024204 (UMLS CUI [1,1])
C0027627 (UMLS CUI [1,2])
metastases
Item
5. patient has evidence of distant metastases
boolean
C0027627 (UMLS CUI [1])
karnofsky performance status
Item
6. karnofsky performance status less than 80% within 60 days prior to study
boolean
C0206065 (UMLS CUI [1])
mammography
Item
7. ipsilateral mammogram done greater than 6 months prior to study
boolean
C0024671 (UMLS CUI [1])
pregnancy, hcg positive
Item
8. women of childbearing potential with a positive serum beta human chorionic gonadotropin (hcg)
boolean
C0032961 (UMLS CUI [1])
compliance and mental disorders
Item
9. patient has a history of dementia, psychosis or other disorder affecting their mental status to the point where they cannot consent or comply with study guidelines
boolean
C0004936 (UMLS CUI [1,1])
C1321605 (UMLS CUI [1,2])
BMI
Item
10. bmi < 21
boolean
C1305855 (UMLS CUI [1])
weight
Item
11. weight < 100 lbs
boolean
C0005910 (UMLS CUI [1])
weight loss
Item
12. weight loss >= 10% in the last 3 months (mos)
boolean
C1262477 (UMLS CUI [1])
cancer history
Item
13. prior invasive non-breast malignancy (except non-melanomatous skin cancer, carcinoma in situ of the cervix) unless disease free for a minimum of 2 years prior to registration
boolean
C0262926 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
multifocal breast cancer
Item
14. two or more breast cancers not resectable through a single lumpectomy incision
boolean
C0678222 (UMLS CUI [1,1])
C0205292 (UMLS CUI [1,2])
C0024885 (UMLS CUI [2])
sarcoma or lymphoma
Item
15. non-epithelial breast malignancies such as sarcoma or lymphoma
boolean
C1261473 (UMLS CUI [1])
C0024299 (UMLS CUI [2])
prior breast cancer therapy
Item
16. prior radiotherapy to the ipsilateral breast or prior radiation to the region of the breast that would result in overlap of radiation therapy fields
boolean
C0678222 (UMLS CUI [1,1])
C0087111 (UMLS CUI [1,2])
comorbidities
Item
17. severe, active co-morbidity, defined as follows:
boolean
C0009488 (UMLS CUI [1])
unstable angina and/or congestive heart failure
Item
1. unstable angina and/or congestive heart failure requiring hospitalization within the last 6 months
boolean
C0018802 (UMLS CUI [1])
C0002965 (UMLS CUI [2])
myocardial infarction
Item
2. transmural myocardial infarction within the last 6 months
boolean
C0027051 (UMLS CUI [1])
current infection therapy, antibiotics
Item
3. acute bacterial or fungal infection requiring intravenous antibiotics at the time of registration
boolean
C0009450 (UMLS CUI [1])
C0003232 (UMLS CUI [2])
respiratory illness
Item
4. chronic obstructive pulmonary disease exacerbation or other respiratory illness requiring hospitalization or precluding study therapy within 30 days before registration
boolean
C0035204 (UMLS CUI [1])
C0024117 (UMLS CUI [2])
hepatic insufficiency
Item
5. hepatic insufficiency resulting in clinical jaundice and/or coagulation defects; note, however, that laboratory tests for liver function and coagulation parameters are not required for entry into this protocol
boolean
C1306571 (UMLS CUI [1])
HIV or AIDS
Item
6. acquired immune deficiency syndrome (aids) or hiv positive based upon current cdc definition; note, however, that hiv testing is not required for entry into this protocol; the need to exclude patients with aids or hiv from this protocol is necessary because anti-retrovirals may alter patient metabolism
boolean
C0019699 (UMLS CUI [1,1])
C0001175 (UMLS CUI [1,2])
skin diseases
Item
18. active systemic lupus, erythematosus, or any history of scleroderma, dermatomyositis with active rash
boolean
C1123023 (UMLS CUI [1,1])
C0012634 (UMLS CUI [1,2])
gastrointestinal disorder
Item
19. active gastrointestinal/malabsorption disorder at the discretion of the principal investigator
boolean
C0017178 (UMLS CUI [1])
inflammatory bowel disease
Item
1. inflammatory bowel disease
boolean
C0021390 (UMLS CUI [1])
celiac disease
Item
2. celiac disease
boolean
C0007570 (UMLS CUI [1])
chronic pancreatitis
Item
3. chronic pancreatitis
boolean
C0030305 (UMLS CUI [1])
chronic diarrhea or vomiting
Item
4. chronic diarrhea or vomiting
boolean
C0042963 (UMLS CUI [1])
C0011991 (UMLS CUI [2])
eating disorders
Item
5. active eating disorder
boolean
C0013473 (UMLS CUI [1])
creatinine
Item
20. creatinine >= 1.7
boolean
C0201976 (UMLS CUI [1])
use of steroids
Item
21. current use of steroids
boolean
C0038317 (UMLS CUI [1])
pituitary tumors
Item
22. pituitary secreting tumors up to physician discretion
boolean
C0032005 (UMLS CUI [1,1])
C0006826 (UMLS CUI [1,2])
drug/alcohol dependence
Item
23. active drug/alcohol dependence or abuse history
boolean
C0038580 (UMLS CUI [1])
C0085762 (UMLS CUI [2])
informed consent not possible
Item
24. decisionally impaired patients
boolean
C0021430 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
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