ID

42562

Descripción

Fingernails in Evaluating Bone Health in Postmenopausal Women With Breast Cancer Undergoing Hormone Therapy on Clinical Trial IBCSG-1-98; ODM derived from: https://clinicaltrials.gov/show/NCT00899288

Link

https://clinicaltrials.gov/show/NCT00899288

Palabras clave

Versiones (2)
  1. 19/1/17 19/1/17 -
  2. 2/9/21 2/9/21 -
Subido en

2 de septiembre de 2021

DOI

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Licencia

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00899288

Inglés

Eligibility Breast Cancer NCT00899288

1 formularios  
Criteria
Descripción

Criteria

enrolled on protocol ibcsg-1-98
Descripción

Enrollment

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1516879
currently receiving (i.e., have not yet completed) 5 years of treatment with tamoxifen or letrozole and expected to receive ≥ 6 months of additional treatment on protocol ibcsg-1-98
Descripción

Tamoxifen | letrozole | Additional Therapy Expected

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0039286
UMLS CUI [2]
C0246421
UMLS CUI [3,1]
C1706712
UMLS CUI [3,2]
C1517001
no recurrent breast cancer or second primary cancer
Descripción

Breast cancer recurrent | Second Primary Cancers

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0278493
UMLS CUI [2]
C0751623
no known bone disease (including osteomalacia or osteogenesis imperfecta)
Descripción

Bone Diseases | Osteomalacia | Osteogenesis Imperfecta

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0005940
UMLS CUI [2]
C0029442
UMLS CUI [3]
C0029434
hormone receptor status
Descripción

Hormone Receptor Status

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
estrogen and/or progesterone receptor positive tumor
Descripción

Estrogen receptor positive tumor | Progesterone receptor positive tumor

Tipo de datos

boolean

Alias
UMLS CUI [1]
C1562312
UMLS CUI [2]
C1562928
patient characteristics:
Descripción

Client Characteristics

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0815172
female
Descripción

Gender

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0079399
postmenopausal
Descripción

Postmenopausal state

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0232970
no uncontrolled thyroid or parathyroid disease, cushing's disease, or other pituitary diseases
Descripción

Thyroid Disease Uncontrolled | Parathyroid Disease Uncontrolled | Cushing's disease | Pituitary Diseases

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0040128
UMLS CUI [1,2]
C0205318
UMLS CUI [2,1]
C0030517
UMLS CUI [2,2]
C0205318
UMLS CUI [3]
C0221406
UMLS CUI [4]
C0032002
no malabsorption syndrome or clinically relevant vitamin d deficiency
Descripción

Malabsorption Syndrome | Vitamin D Deficiency Relevant Clinical

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0024523
UMLS CUI [2,1]
C0042870
UMLS CUI [2,2]
C2347946
UMLS CUI [2,3]
C0205210
prior concurrent therapy:
Descripción

Therapeutic procedure

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Descripción

disease characteristic

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0599878
more than 1 year since prior and no concurrent anticonvulsants
Descripción

Anticonvulsants

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0003286
more than 6 months since prior and no concurrent corticosteroids at doses > the equivalent of 5 mg/day of prednisone for > 2 weeks total
Descripción

Adrenal Cortex Hormones Dose | Prednisone U/day

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0001617
UMLS CUI [1,2]
C0178602
UMLS CUI [2,1]
C0032952
UMLS CUI [2,2]
C0456683
no prior or concurrent sodium fluoride at daily doses ≥ 5 mg/day for > 1 month
Descripción

Sodium Fluoride Dose U/day

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0037508
UMLS CUI [1,2]
C0178602
UMLS CUI [1,3]
C0456683
more than 12 months since prior and no concurrent anabolic steroids
Descripción

Anabolic steroids

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0002845
more than 6 months since any prior drug for the prevention of osteoporosis (excluding calcium or cholecalciferol [vitamin d])
Descripción

Pharmaceutical Preparations Prevention Osteoporosis | Calcium | Cholecalciferol | Vitamin D

Tipo de datos

boolean

Alias
UMLS CUI [1,1]
C0013227
UMLS CUI [1,2]
C2700409
UMLS CUI [1,3]
C0029456
UMLS CUI [2]
C0006675
UMLS CUI [3]
C0008318
UMLS CUI [4]
C0042866
concurrent warfarin allowed provided duration of treatment is no more than 4 weeks
Descripción

Warfarin

Tipo de datos

boolean

Alias
UMLS CUI [1]
C0043031
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Similar models

Eligibility Breast Cancer NCT00899288

1 formularios
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Enrollment
Item
enrolled on protocol ibcsg-1-98
boolean
C1516879 (UMLS CUI [1])
Tamoxifen | letrozole | Additional Therapy Expected
Item
currently receiving (i.e., have not yet completed) 5 years of treatment with tamoxifen or letrozole and expected to receive ≥ 6 months of additional treatment on protocol ibcsg-1-98
boolean
C0039286 (UMLS CUI [1])
C0246421 (UMLS CUI [2])
C1706712 (UMLS CUI [3,1])
C1517001 (UMLS CUI [3,2])
Breast cancer recurrent | Second Primary Cancers
Item
no recurrent breast cancer or second primary cancer
boolean
C0278493 (UMLS CUI [1])
C0751623 (UMLS CUI [2])
Bone Diseases | Osteomalacia | Osteogenesis Imperfecta
Item
no known bone disease (including osteomalacia or osteogenesis imperfecta)
boolean
C0005940 (UMLS CUI [1])
C0029442 (UMLS CUI [2])
C0029434 (UMLS CUI [3])
Hormone Receptor Status
Item
hormone receptor status
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
Estrogen receptor positive tumor | Progesterone receptor positive tumor
Item
estrogen and/or progesterone receptor positive tumor
boolean
C1562312 (UMLS CUI [1])
C1562928 (UMLS CUI [2])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Gender
Item
female
boolean
C0079399 (UMLS CUI [1])
Postmenopausal state
Item
postmenopausal
boolean
C0232970 (UMLS CUI [1])
Thyroid Disease Uncontrolled | Parathyroid Disease Uncontrolled | Cushing's disease | Pituitary Diseases
Item
no uncontrolled thyroid or parathyroid disease, cushing's disease, or other pituitary diseases
boolean
C0040128 (UMLS CUI [1,1])
C0205318 (UMLS CUI [1,2])
C0030517 (UMLS CUI [2,1])
C0205318 (UMLS CUI [2,2])
C0221406 (UMLS CUI [3])
C0032002 (UMLS CUI [4])
Malabsorption Syndrome | Vitamin D Deficiency Relevant Clinical
Item
no malabsorption syndrome or clinically relevant vitamin d deficiency
boolean
C0024523 (UMLS CUI [1])
C0042870 (UMLS CUI [2,1])
C2347946 (UMLS CUI [2,2])
C0205210 (UMLS CUI [2,3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
disease characteristic
Item
see disease characteristics
boolean
C0599878 (UMLS CUI [1])
Anticonvulsants
Item
more than 1 year since prior and no concurrent anticonvulsants
boolean
C0003286 (UMLS CUI [1])
Adrenal Cortex Hormones Dose | Prednisone U/day
Item
more than 6 months since prior and no concurrent corticosteroids at doses > the equivalent of 5 mg/day of prednisone for > 2 weeks total
boolean
C0001617 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0032952 (UMLS CUI [2,1])
C0456683 (UMLS CUI [2,2])
Sodium Fluoride Dose U/day
Item
no prior or concurrent sodium fluoride at daily doses ≥ 5 mg/day for > 1 month
boolean
C0037508 (UMLS CUI [1,1])
C0178602 (UMLS CUI [1,2])
C0456683 (UMLS CUI [1,3])
Anabolic steroids
Item
more than 12 months since prior and no concurrent anabolic steroids
boolean
C0002845 (UMLS CUI [1])
Pharmaceutical Preparations Prevention Osteoporosis | Calcium | Cholecalciferol | Vitamin D
Item
more than 6 months since any prior drug for the prevention of osteoporosis (excluding calcium or cholecalciferol [vitamin d])
boolean
C0013227 (UMLS CUI [1,1])
C2700409 (UMLS CUI [1,2])
C0029456 (UMLS CUI [1,3])
C0006675 (UMLS CUI [2])
C0008318 (UMLS CUI [3])
C0042866 (UMLS CUI [4])
Warfarin
Item
concurrent warfarin allowed provided duration of treatment is no more than 4 weeks
boolean
C0043031 (UMLS CUI [1])
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