ID

43528

Description

S0307A, Long-Term Bone Quality in Women With Breast Cancer Enrolled on Clinical Trial SWOG-S0307; ODM derived from: https://clinicaltrials.gov/show/NCT00873808

Lien

https://clinicaltrials.gov/show/NCT00873808

Mots-clés

Versions (2)
  1. 23/10/2017 23/10/2017 -
  2. 20/09/2021 20/09/2021 -
Détendeur de droits

See clinicaltrials.gov

Téléchargé le

20 septembre 2021

DOI

Pour une demande vous connecter.

Licence

Creative Commons BY 4.0
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Eligibility Breast Cancer NCT00873808

Anglais

Eligibility Breast Cancer NCT00873808

1 Formulaires  
Criteria
Description

Criteria

concurrently enrolled on clinical trial swog-s0307 and receiving bisphosphonates as adjuvant therapy for primary breast cancer
Description

Enrollment in clinical trial SWOG | Diphosphonates | Adjuvant therapy Breast Carcinoma Primary

Type de données

boolean

Alias
UMLS CUI [1,1]
C4041024
UMLS CUI [1,2]
C1519429
UMLS CUI [2]
C0012544
UMLS CUI [3,1]
C0677850
UMLS CUI [3,2]
C0678222
UMLS CUI [3,3]
C0205225
no rickets, osteogenesis imperfecta, osteosclerosis, or osteomalacia
Description

Exclusion Criteria | Rickets | Osteogenesis Imperfecta | Osteosclerosis | Osteomalacia

Type de données

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2]
C0035579
UMLS CUI [3]
C0029434
UMLS CUI [4]
C0029464
UMLS CUI [5]
C0029442
no bone fracture since the age of 21 years unless it was caused by trauma
Description

Exclusion Bone Fracture | Exception Bone Fracture caused by Trauma

Type de données

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0016658
UMLS CUI [2,1]
C1705847
UMLS CUI [2,2]
C0016658
UMLS CUI [2,3]
C0015127
UMLS CUI [2,4]
C3714660
hormone receptor status not specified
Description

Hormone Receptor Status Unspecified

Type de données

boolean

Alias
UMLS CUI [1,1]
C0019929
UMLS CUI [1,2]
C0449438
UMLS CUI [1,3]
C0205370
patient characteristics:
Description

Client Characteristics

Type de données

boolean

Alias
UMLS CUI [1]
C0815172
menopausal status not specified
Description

Menopausal Status Unspecified

Type de données

boolean

Alias
UMLS CUI [1,1]
C3829127
UMLS CUI [1,2]
C0205370
weight < 300 lbs
Description

Body Weight

Type de données

boolean

Alias
UMLS CUI [1]
C0005910
no hyperparathyroidism
Description

Exclusion Hyperparathyroidism

Type de données

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0020502
no serious concurrent or prior anorexia nervosa diagnosed by a physician and causing abnormal menstruation
Description

Exclusion Anorexia Nervosa Serious | Exclusion Anorexia Nervosa Causing Abnormal Menstruation

Type de données

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0003125
UMLS CUI [1,3]
C0205404
UMLS CUI [2,1]
C2828389
UMLS CUI [2,2]
C0003125
UMLS CUI [2,3]
C0678227
UMLS CUI [2,4]
C0025345
no history of hypersensitivity to tetracycline or demeclocycline
Description

Exclusion Criteria | Tetracycline allergy | Demeclocycline allergy

Type de données

boolean

Alias
UMLS CUI [1]
C0680251
UMLS CUI [2]
C0039645
UMLS CUI [3]
C0571502
prior concurrent therapy:
Description

Therapeutic procedure

Type de données

boolean

Alias
UMLS CUI [1]
C0087111
see disease characteristics
Description

ID.12

Type de données

boolean

more than 10 years since prior prednisone at a dose above 5 mg/day for ≥ 3 months
Description

Prednisone Previous Dose U/day

Type de données

boolean

Alias
UMLS CUI [1,1]
C0032952
UMLS CUI [1,2]
C0205156
UMLS CUI [1,3]
C0178602
UMLS CUI [1,4]
C0456683
no prior prednisone before diagnosis of breast cancer
Description

Exclusion | Prednisone Before Diagnosis Breast Carcinoma

Type de données

boolean

Alias
UMLS CUI [1]
C2828389
UMLS CUI [2,1]
C0032952
UMLS CUI [2,2]
C0332152
UMLS CUI [2,3]
C0011900
UMLS CUI [2,4]
C0678222
no prior bisphosphonate therapy
Description

Exclusion Diphosphonates

Type de données

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0012544
no concurrent anticonvulsant medications
Description

Exclusion Anticonvulsants

Type de données

boolean

Alias
UMLS CUI [1,1]
C2828389
UMLS CUI [1,2]
C0003286
Retour au début de la page

Similar models

Eligibility Breast Cancer NCT00873808

1 Formulaires
Name
Type
Description | Question | Decode (Coded Value)
Type de données
Alias
Item Group
Enrollment in clinical trial SWOG | Diphosphonates | Adjuvant therapy Breast Carcinoma Primary
Item
concurrently enrolled on clinical trial swog-s0307 and receiving bisphosphonates as adjuvant therapy for primary breast cancer
boolean
C4041024 (UMLS CUI [1,1])
C1519429 (UMLS CUI [1,2])
C0012544 (UMLS CUI [2])
C0677850 (UMLS CUI [3,1])
C0678222 (UMLS CUI [3,2])
C0205225 (UMLS CUI [3,3])
Exclusion Criteria | Rickets | Osteogenesis Imperfecta | Osteosclerosis | Osteomalacia
Item
no rickets, osteogenesis imperfecta, osteosclerosis, or osteomalacia
boolean
C0680251 (UMLS CUI [1])
C0035579 (UMLS CUI [2])
C0029434 (UMLS CUI [3])
C0029464 (UMLS CUI [4])
C0029442 (UMLS CUI [5])
Exclusion Bone Fracture | Exception Bone Fracture caused by Trauma
Item
no bone fracture since the age of 21 years unless it was caused by trauma
boolean
C2828389 (UMLS CUI [1,1])
C0016658 (UMLS CUI [1,2])
C1705847 (UMLS CUI [2,1])
C0016658 (UMLS CUI [2,2])
C0015127 (UMLS CUI [2,3])
C3714660 (UMLS CUI [2,4])
Hormone Receptor Status Unspecified
Item
hormone receptor status not specified
boolean
C0019929 (UMLS CUI [1,1])
C0449438 (UMLS CUI [1,2])
C0205370 (UMLS CUI [1,3])
Client Characteristics
Item
patient characteristics:
boolean
C0815172 (UMLS CUI [1])
Menopausal Status Unspecified
Item
menopausal status not specified
boolean
C3829127 (UMLS CUI [1,1])
C0205370 (UMLS CUI [1,2])
Body Weight
Item
weight < 300 lbs
boolean
C0005910 (UMLS CUI [1])
Exclusion Hyperparathyroidism
Item
no hyperparathyroidism
boolean
C2828389 (UMLS CUI [1,1])
C0020502 (UMLS CUI [1,2])
Exclusion Anorexia Nervosa Serious | Exclusion Anorexia Nervosa Causing Abnormal Menstruation
Item
no serious concurrent or prior anorexia nervosa diagnosed by a physician and causing abnormal menstruation
boolean
C2828389 (UMLS CUI [1,1])
C0003125 (UMLS CUI [1,2])
C0205404 (UMLS CUI [1,3])
C2828389 (UMLS CUI [2,1])
C0003125 (UMLS CUI [2,2])
C0678227 (UMLS CUI [2,3])
C0025345 (UMLS CUI [2,4])
Exclusion Criteria | Tetracycline allergy | Demeclocycline allergy
Item
no history of hypersensitivity to tetracycline or demeclocycline
boolean
C0680251 (UMLS CUI [1])
C0039645 (UMLS CUI [2])
C0571502 (UMLS CUI [3])
Therapeutic procedure
Item
prior concurrent therapy:
boolean
C0087111 (UMLS CUI [1])
ID.12
Item
see disease characteristics
boolean
Prednisone Previous Dose U/day
Item
more than 10 years since prior prednisone at a dose above 5 mg/day for ≥ 3 months
boolean
C0032952 (UMLS CUI [1,1])
C0205156 (UMLS CUI [1,2])
C0178602 (UMLS CUI [1,3])
C0456683 (UMLS CUI [1,4])
Exclusion | Prednisone Before Diagnosis Breast Carcinoma
Item
no prior prednisone before diagnosis of breast cancer
boolean
C2828389 (UMLS CUI [1])
C0032952 (UMLS CUI [2,1])
C0332152 (UMLS CUI [2,2])
C0011900 (UMLS CUI [2,3])
C0678222 (UMLS CUI [2,4])
Exclusion Diphosphonates
Item
no prior bisphosphonate therapy
boolean
C2828389 (UMLS CUI [1,1])
C0012544 (UMLS CUI [1,2])
Exclusion Anticonvulsants
Item
no concurrent anticonvulsant medications
boolean
C2828389 (UMLS CUI [1,1])
C0003286 (UMLS CUI [1,2])
Retour au début de la page 

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