Eligibility Menopause NCT00361075

  1. StudyEvent: Eligibility
    1. Eligibility Menopause NCT00361075
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
have demonstrated an interest to participate in the ert trial
Description

interest to participate

Data type

boolean

Alias
UMLS CUI [1]
C2348568
be premenopausal (have menstrual period in previous three months) prior to start of observational arm
Description

premenopausal

Data type

boolean

Alias
UMLS CUI [1]
C0279752
prior to start of interventional arm (ert), the women must be postmenopausal (have not had a menstrual cycle in the past twelve months and fsh >30)
Description

postmenopausal

Data type

boolean

Alias
UMLS CUI [1]
C0232970
be between the ages of 47 and 55
Description

age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
not be taking any form of estrogen replacement
Description

estrogen

Data type

boolean

Alias
UMLS CUI [1]
C3541386
have an intact uterus and at least one ovary and normal screening mammogram in the 12 months prior to starting ert
Description

intact uterus and at least one ovary and normal screening mammogram

Data type

boolean

Alias
UMLS CUI [1]
C0024671
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
body mass index (kg/m2) greater than 40 kg/m2
Description

bmi

Data type

boolean

Alias
UMLS CUI [1]
C1305855
history of diabetes mellitus or fasting >110 mg/dl at screening
Description

diabetes mellitus

Data type

boolean

Alias
UMLS CUI [1]
C0011849
abnormal fasting ldl or triglyceride
Description

LDL or Triglyceride

Data type

boolean

Alias
UMLS CUI [1]
C0428474
UMLS CUI [2]
C0041004
use of lipid lowering medications, beta-blockers, birth control pills
Description

lipid lowering medications, beta-blockers, birth control pills

Data type

boolean

Alias
UMLS CUI [1]
C0086440
UMLS CUI [2]
C0001645
UMLS CUI [3]
C0009905
active liver disease (recent history of active hepatitis, jaundice, scleral icterus, and/or elevated liver function tests
Description

liver disease

Data type

boolean

Alias
UMLS CUI [1]
C0085605
history of breast, endometrial or ovarian cancer
Description

malignancy

Data type

boolean

Alias
UMLS CUI [1]
C0006826
history of thrombotic disorder (past history of pulmonary embolus or deep venous thrombosis) or known history of cad
Description

thrombosis

Data type

boolean

Alias
UMLS CUI [1]
C0040053

Similar models

Eligibility Menopause NCT00361075

  1. StudyEvent: Eligibility
    1. Eligibility Menopause NCT00361075
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
interest to participate
Item
have demonstrated an interest to participate in the ert trial
boolean
C2348568 (UMLS CUI [1])
premenopausal
Item
be premenopausal (have menstrual period in previous three months) prior to start of observational arm
boolean
C0279752 (UMLS CUI [1])
postmenopausal
Item
prior to start of interventional arm (ert), the women must be postmenopausal (have not had a menstrual cycle in the past twelve months and fsh >30)
boolean
C0232970 (UMLS CUI [1])
age
Item
be between the ages of 47 and 55
boolean
C0001779 (UMLS CUI [1])
estrogen
Item
not be taking any form of estrogen replacement
boolean
C3541386 (UMLS CUI [1])
intact uterus and at least one ovary and normal screening mammogram
Item
have an intact uterus and at least one ovary and normal screening mammogram in the 12 months prior to starting ert
boolean
C0024671 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
bmi
Item
body mass index (kg/m2) greater than 40 kg/m2
boolean
C1305855 (UMLS CUI [1])
diabetes mellitus
Item
history of diabetes mellitus or fasting >110 mg/dl at screening
boolean
C0011849 (UMLS CUI [1])
LDL or Triglyceride
Item
abnormal fasting ldl or triglyceride
boolean
C0428474 (UMLS CUI [1])
C0041004 (UMLS CUI [2])
lipid lowering medications, beta-blockers, birth control pills
Item
use of lipid lowering medications, beta-blockers, birth control pills
boolean
C0086440 (UMLS CUI [1])
C0001645 (UMLS CUI [2])
C0009905 (UMLS CUI [3])
liver disease
Item
active liver disease (recent history of active hepatitis, jaundice, scleral icterus, and/or elevated liver function tests
boolean
C0085605 (UMLS CUI [1])
malignancy
Item
history of breast, endometrial or ovarian cancer
boolean
C0006826 (UMLS CUI [1])
thrombosis
Item
history of thrombotic disorder (past history of pulmonary embolus or deep venous thrombosis) or known history of cad
boolean
C0040053 (UMLS CUI [1])