ID

30571

Description

Multi-centre Clinical Trial on Hormone Replacement Treatment in China; ODM derived from: https://clinicaltrials.gov/show/NCT01698164

Link

https://clinicaltrials.gov/show/NCT01698164

Keywords

Versions (1)
  1. 6/15/18 6/15/18 -
Copyright Holder

See clinicaltrials.gov

Uploaded on

June 15, 2018

DOI

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License

Creative Commons BY 4.0
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Eligibility Menopausal Syndrome NCT01698164

English

Eligibility Menopausal Syndrome NCT01698164

1 forms  
Inclusion Criteria
Description

Inclusion Criteria

Alias
UMLS CUI
C1512693
going through amenorrhea above 6 months and within 5 years,
Description

Amenorrhea Duration

Data type

boolean

Alias
UMLS CUI [1,1]
C0002453
UMLS CUI [1,2]
C0449238
aged 40 to 60 years,
Description

Age

Data type

boolean

Alias
UMLS CUI [1]
C0001779
going though postmenopausal symptoms,
Description

Postmenopausal syndrome

Data type

boolean

Alias
UMLS CUI [1]
C0747771
serum e2 concentration <30pg/ml,
Description

Serum estradiol measurement

Data type

boolean

Alias
UMLS CUI [1]
C0474672
serum fsh concentration >40iu/l.
Description

Serum follicle stimulating hormone measurement

Data type

boolean

Alias
UMLS CUI [1]
C0455276
Exclusion Criteria
Description

Exclusion Criteria

Alias
UMLS CUI
C0680251
uterine fibroid diameter≥5cm,
Description

Uterine Fibroid Diameter

Data type

boolean

Alias
UMLS CUI [1,1]
C0042133
UMLS CUI [1,2]
C1301886
history of diabetes or hypertension,
Description

Diabetes Mellitus | Hypertensive disease

Data type

boolean

Alias
UMLS CUI [1]
C0011849
UMLS CUI [2]
C0020538
history of thromboembolism, severe endometriosis, epilepsy, asthma, hyperprolactinemia,
Description

Thromboembolism | Endometriosis Severe | Epilepsy | Asthma | Hyperprolactinemia

Data type

boolean

Alias
UMLS CUI [1]
C0040038
UMLS CUI [2,1]
C0014175
UMLS CUI [2,2]
C0205082
UMLS CUI [3]
C0014544
UMLS CUI [4]
C0004096
UMLS CUI [5]
C0020514
first degree relative had a history of breast cancer,
Description

First Degree Relative Breast Carcinoma

Data type

boolean

Alias
UMLS CUI [1,1]
C1517194
UMLS CUI [1,2]
C0678222
being in severe or unstable condition of somatic diseases,
Description

Disease Somatic Severe | Disease Somatic Unstable

Data type

boolean

Alias
UMLS CUI [1,1]
C0012634
UMLS CUI [1,2]
C2986476
UMLS CUI [1,3]
C0205082
UMLS CUI [2,1]
C0012634
UMLS CUI [2,2]
C2986476
UMLS CUI [2,3]
C0443343
receiving hrt in the past 3 month,
Description

Hormone replacement therapy

Data type

boolean

Alias
UMLS CUI [1]
C0282402
drug or alcohol abuse in the past 3 month,
Description

Substance Use Disorders

Data type

boolean

Alias
UMLS CUI [1]
C0038586
endometrial thickness ≥0.5cm after withdrawal bleeding,
Description

Thickness of endometrium Post Withdrawal bleeding

Data type

boolean

Alias
UMLS CUI [1,1]
C0237027
UMLS CUI [1,2]
C0687676
UMLS CUI [1,3]
C0152010
being allergic to the medicine,
Description

Drug Allergy

Data type

boolean

Alias
UMLS CUI [1]
C0013182
participating in other clinical trials within 1 month ago.
Description

Study Subject Participation Status

Data type

boolean

Alias
UMLS CUI [1]
C2348568
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Similar models

Eligibility Menopausal Syndrome NCT01698164

1 forms
Name
Type
Description | Question | Decode (Coded Value)
Data type
Alias
Item Group
C1512693 (UMLS CUI)
Amenorrhea Duration
Item
going through amenorrhea above 6 months and within 5 years,
boolean
C0002453 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
Age
Item
aged 40 to 60 years,
boolean
C0001779 (UMLS CUI [1])
Postmenopausal syndrome
Item
going though postmenopausal symptoms,
boolean
C0747771 (UMLS CUI [1])
Serum estradiol measurement
Item
serum e2 concentration <30pg/ml,
boolean
C0474672 (UMLS CUI [1])
Serum follicle stimulating hormone measurement
Item
serum fsh concentration >40iu/l.
boolean
C0455276 (UMLS CUI [1])
Item Group
C0680251 (UMLS CUI)
Uterine Fibroid Diameter
Item
uterine fibroid diameter≥5cm,
boolean
C0042133 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
Diabetes Mellitus | Hypertensive disease
Item
history of diabetes or hypertension,
boolean
C0011849 (UMLS CUI [1])
C0020538 (UMLS CUI [2])
Thromboembolism | Endometriosis Severe | Epilepsy | Asthma | Hyperprolactinemia
Item
history of thromboembolism, severe endometriosis, epilepsy, asthma, hyperprolactinemia,
boolean
C0040038 (UMLS CUI [1])
C0014175 (UMLS CUI [2,1])
C0205082 (UMLS CUI [2,2])
C0014544 (UMLS CUI [3])
C0004096 (UMLS CUI [4])
C0020514 (UMLS CUI [5])
First Degree Relative Breast Carcinoma
Item
first degree relative had a history of breast cancer,
boolean
C1517194 (UMLS CUI [1,1])
C0678222 (UMLS CUI [1,2])
Disease Somatic Severe | Disease Somatic Unstable
Item
being in severe or unstable condition of somatic diseases,
boolean
C0012634 (UMLS CUI [1,1])
C2986476 (UMLS CUI [1,2])
C0205082 (UMLS CUI [1,3])
C0012634 (UMLS CUI [2,1])
C2986476 (UMLS CUI [2,2])
C0443343 (UMLS CUI [2,3])
Hormone replacement therapy
Item
receiving hrt in the past 3 month,
boolean
C0282402 (UMLS CUI [1])
Substance Use Disorders
Item
drug or alcohol abuse in the past 3 month,
boolean
C0038586 (UMLS CUI [1])
Thickness of endometrium Post Withdrawal bleeding
Item
endometrial thickness ≥0.5cm after withdrawal bleeding,
boolean
C0237027 (UMLS CUI [1,1])
C0687676 (UMLS CUI [1,2])
C0152010 (UMLS CUI [1,3])
Drug Allergy
Item
being allergic to the medicine,
boolean
C0013182 (UMLS CUI [1])
Study Subject Participation Status
Item
participating in other clinical trials within 1 month ago.
boolean
C2348568 (UMLS CUI [1])
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