ID

43774

Beschrijving

Development of Vitamin D as a Therapy for Breast Cancer - Phase II; ODM derived from: https://clinicaltrials.gov/show/NCT00656019

Link

https://clinicaltrials.gov/show/NCT00656019

Trefwoorden

Versies (2)
  1. 09-10-17 09-10-17 -
  2. 20-09-21 20-09-21 -
Houder van rechten

See clinicaltrials.gov

Geüploaded op

20 september 2021

DOI

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Licentie

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00656019

Engels

Eligibility Breast Cancer NCT00656019

1 Formulieren  
Inclusion Criteria
Beschrijving

Inclusion Criteria

Alias
UMLS CUI
C1512693
women undergoing core needle biopsy for a breast abnormality suspicious for breast cancer. women who have undergone a core needle biopsy demonstrating breast cancer who have not yet had any further therapy are also eligible so long as their core needle biopsy is available for analysis.
Beschrijving

Gender | Core needle biopsy | Abnormality of the breast Suspicious Breast Carcinoma | Breast Carcinoma Core needle biopsy

Datatype

boolean

Alias
UMLS CUI [1]
C0079399
UMLS CUI [2]
C1318309
UMLS CUI [3,1]
C4025829
UMLS CUI [3,2]
C0750493
UMLS CUI [3,3]
C0678222
UMLS CUI [4,1]
C0678222
UMLS CUI [4,2]
C1318309
no prior therapy for breast cancer.
Beschrijving

Prior Therapy Absent Breast Carcinoma

Datatype

boolean

Alias
UMLS CUI [1,1]
C1514463
UMLS CUI [1,2]
C0332197
UMLS CUI [1,3]
C0678222
age 18 years or older.
Beschrijving

Age

Datatype

boolean

Alias
UMLS CUI [1]
C0001779
ability to understand and the willingness to sign a written informed consent document.
Beschrijving

Comprehension Informed Consent | Informed Consent Willing

Datatype

boolean

Alias
UMLS CUI [1,1]
C0162340
UMLS CUI [1,2]
C0021430
UMLS CUI [2,1]
C0021430
UMLS CUI [2,2]
C0600109
signed informed consent
Beschrijving

Informed Consent

Datatype

boolean

Alias
UMLS CUI [1]
C0021430
Exclusion Criteria
Beschrijving

Exclusion Criteria

Alias
UMLS CUI
C0680251
history of parathyroid disease, hypercalcemia, or kidney stones.
Beschrijving

Parathyroid Diseases | Hypercalcemia | Kidney Calculi

Datatype

boolean

Alias
UMLS CUI [1]
C0030517
UMLS CUI [2]
C0020437
UMLS CUI [3]
C0022650
supplemental vitamin d other than from a standard multiple vitamin or from standard formulations of calcium and vitamin d (e.g. calcium citrate with vitamin d) within the prior 6 months.
Beschrijving

Vitamin D supplement | Exception Standard Multivitamin preparation | Exception Standard Calcium + vitamin D | Exception Calcium Citrate / Vitamin D

Datatype

boolean

Alias
UMLS CUI [1]
C3541352
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C1442989
UMLS CUI [2,3]
C0301532
UMLS CUI [3,1]
C1705847
UMLS CUI [3,2]
C1442989
UMLS CUI [3,3]
C0719107
UMLS CUI [4,1]
C1705847
UMLS CUI [4,2]
C0719098
history of renal failure requiring dialysis or kidney transplantation.
Beschrijving

Kidney Failure Requirement Dialysis | Kidney Failure Requirement Kidney Transplantation

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035078
UMLS CUI [1,2]
C1514873
UMLS CUI [1,3]
C0011946
UMLS CUI [2,1]
C0035078
UMLS CUI [2,2]
C1514873
UMLS CUI [2,3]
C0022671
women who are known to be pregnant or who are nursing. (as vitamin d does not have toxicity to the fetus, a negative pregnancy test is not a requirement to participate in the study.)
Beschrijving

Pregnancy | Breast Feeding

Datatype

boolean

Alias
UMLS CUI [1]
C0032961
UMLS CUI [2]
C0006147
supplemental calcium greater than 600 mg calcium per day during study.
Beschrijving

Calcium supplement U/day

Datatype

boolean

Alias
UMLS CUI [1,1]
C3540037
UMLS CUI [1,2]
C0456683
patients for who initial treatment of their breast cancer will not be with breast conserving surgery or mastectomy.
Beschrijving

First line treatment Breast Carcinoma | Breast-Conserving Surgery Absent | Mastectomy Absent

Datatype

boolean

Alias
UMLS CUI [1,1]
C1708063
UMLS CUI [1,2]
C0678222
UMLS CUI [2,1]
C0917927
UMLS CUI [2,2]
C0332197
UMLS CUI [3,1]
C0024881
UMLS CUI [3,2]
C0332197
patients with locally advanced breast cancer
Beschrijving

Locally advanced breast cancer

Datatype

boolean

Alias
UMLS CUI [1]
C3495949
patients planned for neoadjuvant chemotherapy, hormonal therapy, or other systemic therapy.
Beschrijving

Chemotherapy Neoadjuvant Planned | Hormone Therapy Planned | Systemic therapy Planned

Datatype

boolean

Alias
UMLS CUI [1,1]
C0392920
UMLS CUI [1,2]
C0600558
UMLS CUI [1,3]
C1301732
UMLS CUI [2,1]
C0279025
UMLS CUI [2,2]
C1301732
UMLS CUI [3,1]
C1515119
UMLS CUI [3,2]
C1301732
patients planned for preoperative radiation therapy.
Beschrijving

Therapeutic radiology procedure Preoperative Planned

Datatype

boolean

Alias
UMLS CUI [1,1]
C1522449
UMLS CUI [1,2]
C0445204
UMLS CUI [1,3]
C1301732
patients with planned surgical therapy of their breast cancer that would not allow for at least 10 days of vitamin d intervention.
Beschrijving

Operative Surgical Procedure Planned Breast Carcinoma | Vitamin D Intervention Illicit

Datatype

boolean

Alias
UMLS CUI [1,1]
C0543467
UMLS CUI [1,2]
C1301732
UMLS CUI [1,3]
C0678222
UMLS CUI [2,1]
C0042866
UMLS CUI [2,2]
C0184661
UMLS CUI [2,3]
C0332266
any condition potentially interfering with subjects ability to comply with taking study medication.
Beschrijving

Condition Interferes with Investigational New Drugs

Datatype

boolean

Alias
UMLS CUI [1,1]
C0348080
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0013230
any medical condition that would potentially interfere with vitamin d absorption, such as celiac sprue, ulcerative colitis.
Beschrijving

Medical condition Interferes with Vitamin D Absorption | Celiac Disease | Ulcerative Colitis

Datatype

boolean

Alias
UMLS CUI [1,1]
C3843040
UMLS CUI [1,2]
C0521102
UMLS CUI [1,3]
C0042866
UMLS CUI [1,4]
C0237442
UMLS CUI [2]
C0007570
UMLS CUI [3]
C0009324
current participation in another research study that would increase risk to subject, in the opinion of the investigators
Beschrijving

Risk Increased by Study Subject Participation Status

Datatype

boolean

Alias
UMLS CUI [1,1]
C0035647
UMLS CUI [1,2]
C0205217
UMLS CUI [1,3]
C2348568
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Similar models

Eligibility Breast Cancer NCT00656019

1 Formulieren
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Item Group
C1512693 (UMLS CUI)
Gender | Core needle biopsy | Abnormality of the breast Suspicious Breast Carcinoma | Breast Carcinoma Core needle biopsy
Item
women undergoing core needle biopsy for a breast abnormality suspicious for breast cancer. women who have undergone a core needle biopsy demonstrating breast cancer who have not yet had any further therapy are also eligible so long as their core needle biopsy is available for analysis.
boolean
C0079399 (UMLS CUI [1])
C1318309 (UMLS CUI [2])
C4025829 (UMLS CUI [3,1])
C0750493 (UMLS CUI [3,2])
C0678222 (UMLS CUI [3,3])
C0678222 (UMLS CUI [4,1])
C1318309 (UMLS CUI [4,2])
Prior Therapy Absent Breast Carcinoma
Item
no prior therapy for breast cancer.
boolean
C1514463 (UMLS CUI [1,1])
C0332197 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
Age
Item
age 18 years or older.
boolean
C0001779 (UMLS CUI [1])
Comprehension Informed Consent | Informed Consent Willing
Item
ability to understand and the willingness to sign a written informed consent document.
boolean
C0162340 (UMLS CUI [1,1])
C0021430 (UMLS CUI [1,2])
C0021430 (UMLS CUI [2,1])
C0600109 (UMLS CUI [2,2])
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Parathyroid Diseases | Hypercalcemia | Kidney Calculi
Item
history of parathyroid disease, hypercalcemia, or kidney stones.
boolean
C0030517 (UMLS CUI [1])
C0020437 (UMLS CUI [2])
C0022650 (UMLS CUI [3])
Vitamin D supplement | Exception Standard Multivitamin preparation | Exception Standard Calcium + vitamin D | Exception Calcium Citrate / Vitamin D
Item
supplemental vitamin d other than from a standard multiple vitamin or from standard formulations of calcium and vitamin d (e.g. calcium citrate with vitamin d) within the prior 6 months.
boolean
C3541352 (UMLS CUI [1])
C1705847 (UMLS CUI [2,1])
C1442989 (UMLS CUI [2,2])
C0301532 (UMLS CUI [2,3])
C1705847 (UMLS CUI [3,1])
C1442989 (UMLS CUI [3,2])
C0719107 (UMLS CUI [3,3])
C1705847 (UMLS CUI [4,1])
C0719098 (UMLS CUI [4,2])
Kidney Failure Requirement Dialysis | Kidney Failure Requirement Kidney Transplantation
Item
history of renal failure requiring dialysis or kidney transplantation.
boolean
C0035078 (UMLS CUI [1,1])
C1514873 (UMLS CUI [1,2])
C0011946 (UMLS CUI [1,3])
C0035078 (UMLS CUI [2,1])
C1514873 (UMLS CUI [2,2])
C0022671 (UMLS CUI [2,3])
Pregnancy | Breast Feeding
Item
women who are known to be pregnant or who are nursing. (as vitamin d does not have toxicity to the fetus, a negative pregnancy test is not a requirement to participate in the study.)
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
Calcium supplement U/day
Item
supplemental calcium greater than 600 mg calcium per day during study.
boolean
C3540037 (UMLS CUI [1,1])
C0456683 (UMLS CUI [1,2])
First line treatment Breast Carcinoma | Breast-Conserving Surgery Absent | Mastectomy Absent
Item
patients for who initial treatment of their breast cancer will not be with breast conserving surgery or mastectomy.
boolean
C1708063 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
C0917927 (UMLS CUI [2,1])
C0332197 (UMLS CUI [2,2])
C0024881 (UMLS CUI [3,1])
C0332197 (UMLS CUI [3,2])
Locally advanced breast cancer
Item
patients with locally advanced breast cancer
boolean
C3495949 (UMLS CUI [1])
Chemotherapy Neoadjuvant Planned | Hormone Therapy Planned | Systemic therapy Planned
Item
patients planned for neoadjuvant chemotherapy, hormonal therapy, or other systemic therapy.
boolean
C0392920 (UMLS CUI [1,1])
C0600558 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
C0279025 (UMLS CUI [2,1])
C1301732 (UMLS CUI [2,2])
C1515119 (UMLS CUI [3,1])
C1301732 (UMLS CUI [3,2])
Therapeutic radiology procedure Preoperative Planned
Item
patients planned for preoperative radiation therapy.
boolean
C1522449 (UMLS CUI [1,1])
C0445204 (UMLS CUI [1,2])
C1301732 (UMLS CUI [1,3])
Operative Surgical Procedure Planned Breast Carcinoma | Vitamin D Intervention Illicit
Item
patients with planned surgical therapy of their breast cancer that would not allow for at least 10 days of vitamin d intervention.
boolean
C0543467 (UMLS CUI [1,1])
C1301732 (UMLS CUI [1,2])
C0678222 (UMLS CUI [1,3])
C0042866 (UMLS CUI [2,1])
C0184661 (UMLS CUI [2,2])
C0332266 (UMLS CUI [2,3])
Condition Interferes with Investigational New Drugs
Item
any condition potentially interfering with subjects ability to comply with taking study medication.
boolean
C0348080 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0013230 (UMLS CUI [1,3])
Medical condition Interferes with Vitamin D Absorption | Celiac Disease | Ulcerative Colitis
Item
any medical condition that would potentially interfere with vitamin d absorption, such as celiac sprue, ulcerative colitis.
boolean
C3843040 (UMLS CUI [1,1])
C0521102 (UMLS CUI [1,2])
C0042866 (UMLS CUI [1,3])
C0237442 (UMLS CUI [1,4])
C0007570 (UMLS CUI [2])
C0009324 (UMLS CUI [3])
Risk Increased by Study Subject Participation Status
Item
current participation in another research study that would increase risk to subject, in the opinion of the investigators
boolean
C0035647 (UMLS CUI [1,1])
C0205217 (UMLS CUI [1,2])
C2348568 (UMLS CUI [1,3])
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