ID

43834

Description

XELODA and Lapatinib Advanced or Metastatic Breast Cancer Study ID: 100151 Clinical Study ID: EGF100151 Study Title: A Phase III, Randomized, Open-label, Multicenter Study Comparing GW572016 and Capecitabine (XELODA) versus Capecitabine in Women with Refractory Advanced or Metastatic Breast Cancer Clinicaltrials.gov Identifier: NCT00078572 https://clinicaltrials.gov/ct2/show/NCT00078572 Procedure: Demography Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 3 Study Recruitment Status: Completed Generic Name: lapatinib Trade Name: Tyverb,Tykerb,Tycerb Study Indication: Breast Cancer; Neoplasms, Breast

Link

https://clinicaltrials.gov/ct2/show/NCT00078572

Keywords

  1. 5/18/17 5/18/17 -
  2. 9/20/21 9/20/21 -
Uploaded on

September 20, 2021

DOI

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License

Creative Commons BY-NC 3.0

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XELODA and Lapatinib Advanced or Metastatic Breast Cancer Demography NCT00078572

XELODA and Lapatinib Advanced or Metastatic Breast Cancer Demography NCT00078572

Demography
Description

Demography

Alias
UMLS CUI-1
C0011298
Date of assessment
Description

Date of assessment

Data type

date

Alias
UMLS CUI [1]
C2985720
Date of birth
Description

Date of birth

Data type

date

Alias
UMLS CUI [1]
C0421451
Sex
Description

Sex

Data type

text

Alias
UMLS CUI [1]
C0079399
Race
Description

Race

Data type

text

Alias
UMLS CUI [1]
C0034510
Demography for Females
Description

Demography for Females

Alias
UMLS CUI-1
C0011298
UMLS CUI-2
C0086287
Childbearing potential, check one:
Description

Childbearing potential

Data type

text

Alias
UMLS CUI [1]
C3831118
Check all type(s) of contraception used below:
Description

contraception

Data type

integer

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0420837
Contraception used: Other, please specify
Description

Contraception

Data type

text

Alias
UMLS CUI [1,1]
C0700589
UMLS CUI [1,2]
C0420837
Pregnancy test result, check one:
Description

Pregnancy test result

Data type

text

Alias
UMLS CUI [1]
C0032976

Similar models

XELODA and Lapatinib Advanced or Metastatic Breast Cancer Demography NCT00078572

Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
Demography
C0011298 (UMLS CUI-1)
Date of assessment
Item
Date of assessment
date
C2985720 (UMLS CUI [1])
Date of birth
Item
Date of birth
date
C0421451 (UMLS CUI [1])
Item
Sex
text
C0079399 (UMLS CUI [1])
Code List
Sex
CL Item
Male (M)
CL Item
Female (F)
Item
Race
text
C0034510 (UMLS CUI [1])
Code List
Race
CL Item
White, Origins in the original peoples of Europe, the Middle East, Western Russia, Afghanistan, or the white racial groups of Africa. (W)
CL Item
Black, Origins in any of the black racial groups of Africa. (B)
CL Item
Asian, Origins in the original peoples of the Indian subcontinent, the Far East, Southeast Asia, or the Pacific islands (A)
CL Item
American Hispanic, Hispanics of North, Central, or South American origin. (H)
CL Item
Other, People whose racial group is not represented above, or whose predominant origin cannot be determined. (X)
Item Group
Demography for Females
C0011298 (UMLS CUI-1)
C0086287 (UMLS CUI-2)
Item
Childbearing potential, check one:
text
C3831118 (UMLS CUI [1])
Code List
Childbearing potential, check one:
CL Item
Premenarcheal (M)
CL Item
Sterile (of childbearing age) (S)
CL Item
Postmenopausal (P)
CL Item
Potentially able to conceive children (A)
Item
Check all type(s) of contraception used below:
integer
C0700589 (UMLS CUI [1,1])
C0420837 (UMLS CUI [1,2])
Code List
Check all type(s) of contraception used below:
CL Item
Oral contraceptive (1)
CL Item
Intrauterine contraceptive device (2)
CL Item
Depot contraceptive (implants, injectables) (3)
CL Item
Physical barrier 1 (condom, diaphragm) (4)
CL Item
Abstinence (5)
CL Item
Sterilization of male partner (6)
CL Item
None (7)
CL Item
Other (8)
Contraception
Item
Contraception used: Other, please specify
text
C0700589 (UMLS CUI [1,1])
C0420837 (UMLS CUI [1,2])
Item
Pregnancy test result, check one:
text
C0032976 (UMLS CUI [1])
Code List
Pregnancy test result, check one:
CL Item
Positive (P)
CL Item
Negative (N)
CL Item
Not applicable (Not of childbearing potential) (C)

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