Informações:
Falhas:
ID
43046
Descrição
Midlife Cholesterol Study; ODM derived from: https://clinicaltrials.gov/show/NCT00361075
Link
https://clinicaltrials.gov/show/NCT00361075
Palavras-chave
Versões (2)
- 13/01/2016 13/01/2016 -
- 17/09/2021 17/09/2021 -
Titular dos direitos
CC BY-NC 3.0
Transferido a
17 de setembro de 2021
DOI
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Licença
Creative Commons BY-NC 3.0
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Eligibility Menopause NCT00361075
Eligibility Menopause NCT00361075
- StudyEvent: Eligibility
Similar models
Eligibility Menopause NCT00361075
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
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])
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])
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])
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])