ID

16006

Beschreibung

Treatment With Zoledronic Acid in Patients With Breast Cancer, Multiple Myeloma, and Prostate Cancer With Cancer Related Bone Lesions; ODM derived from: https://clinicaltrials.gov/show/NCT00029224

Link

https://clinicaltrials.gov/show/NCT00029224

Stichworte

  1. 02.05.16 02.05.16 -
  2. 26.06.16 26.06.16 -
Hochgeladen am

26. Juni 2016

DOI

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Lizenz

Creative Commons BY 4.0

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Eligibility Breast Cancer NCT00029224

Eligibility Breast Cancer NCT00029224

Inclusion Criteria
Beschreibung

Inclusion Criteria

Alias
UMLS CUI
C1512693
signed informed consent
Beschreibung

Informed Consent

Datentyp

boolean

Alias
UMLS CUI [1]
C0021430
greater than 18 years of age
Beschreibung

age

Datentyp

boolean

Alias
UMLS CUI [1]
C0001779
proof of breast cancer, multiple myeloma or prostate cancer
Beschreibung

breast cancer, multiple myeloma or prostate cancer

Datentyp

boolean

Alias
UMLS CUI [1]
C0678222
UMLS CUI [2]
C0026764
UMLS CUI [3]
C0600139
diagnosis of at least one cancer-related bone lesion
Beschreibung

cancer-related bone lesion

Datentyp

boolean

Alias
UMLS CUI [1]
C0153690
if patient is of child-bearing potential, negative pregnancy test and on a medically recognized form of contraception
Beschreibung

pregnancy test and contraception

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0032976
UMLS CUI [1,2]
C0700589
ecog performance status of 0,1 or 2
Beschreibung

ECOG performance status

Datentyp

boolean

Alias
UMLS CUI [1]
C1520224
ability to read, understand and write english or spanish language
Beschreibung

english or spanish language skills

Datentyp

boolean

Alias
UMLS CUI [1]
C0376245
UMLS CUI [2]
C0037750
normal renal function
Beschreibung

Renal function normal

Datentyp

boolean

Alias
UMLS CUI [1]
C0232804
corrected serum calcium equal to or greater than 8mg/dl exclusion criteria
Beschreibung

serum calcium

Datentyp

boolean

Alias
UMLS CUI [1]
C0728876
clinically symptomatic brain metastases
Beschreibung

symptomatic brain metastases

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0220650
UMLS CUI [1,2]
C0231220
hypersensitivity to zometa or other bisphosphonates
Beschreibung

hypersensitivity to bisphosphonates

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0020517
UMLS CUI [1,2]
C0012544
pregnant or lactating
Beschreibung

pregnant or lactating

Datentyp

boolean

Alias
UMLS CUI [1,1]
C0032961
UMLS CUI [1,2]
C0006147

Ähnliche Modelle

Eligibility Breast Cancer NCT00029224

Name
Typ
Description | Question | Decode (Coded Value)
Datentyp
Alias
Item Group
C1512693 (UMLS CUI)
Informed Consent
Item
signed informed consent
boolean
C0021430 (UMLS CUI [1])
age
Item
greater than 18 years of age
boolean
C0001779 (UMLS CUI [1])
breast cancer, multiple myeloma or prostate cancer
Item
proof of breast cancer, multiple myeloma or prostate cancer
boolean
C0678222 (UMLS CUI [1])
C0026764 (UMLS CUI [2])
C0600139 (UMLS CUI [3])
cancer-related bone lesion
Item
diagnosis of at least one cancer-related bone lesion
boolean
C0153690 (UMLS CUI [1])
pregnancy test and contraception
Item
if patient is of child-bearing potential, negative pregnancy test and on a medically recognized form of contraception
boolean
C0032976 (UMLS CUI [1,1])
C0700589 (UMLS CUI [1,2])
ECOG performance status
Item
ecog performance status of 0,1 or 2
boolean
C1520224 (UMLS CUI [1])
english or spanish language skills
Item
ability to read, understand and write english or spanish language
boolean
C0376245 (UMLS CUI [1])
C0037750 (UMLS CUI [2])
Renal function normal
Item
normal renal function
boolean
C0232804 (UMLS CUI [1])
serum calcium
Item
corrected serum calcium equal to or greater than 8mg/dl exclusion criteria
boolean
C0728876 (UMLS CUI [1])
symptomatic brain metastases
Item
clinically symptomatic brain metastases
boolean
C0220650 (UMLS CUI [1,1])
C0231220 (UMLS CUI [1,2])
hypersensitivity to bisphosphonates
Item
hypersensitivity to zometa or other bisphosphonates
boolean
C0020517 (UMLS CUI [1,1])
C0012544 (UMLS CUI [1,2])
pregnant or lactating
Item
pregnant or lactating
boolean
C0032961 (UMLS CUI [1,1])
C0006147 (UMLS CUI [1,2])

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