Informatie:
Fout:
ID
30571
Beschrijving
Multi-centre Clinical Trial on Hormone Replacement Treatment in China; ODM derived from: https://clinicaltrials.gov/show/NCT01698164
Link
https://clinicaltrials.gov/show/NCT01698164
Trefwoorden
Versies (1)
- 15-06-18 15-06-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
15 juni 2018
DOI
Voor een aanvraag inloggen.
Licentie
Creative Commons BY 4.0
Model Commentaren :
Hier kunt u commentaar leveren op het model. U kunt de tekstballonnen bij de itemgroepen en items gebruiken om er specifiek commentaar op te geven.
Itemgroep Commentaren voor :
Item Commentaren voor :
U moet ingelogd zijn om formulieren te downloaden. AUB inloggen of schrijf u gratis in.
Eligibility Menopausal Syndrome NCT01698164
Eligibility Menopausal Syndrome NCT01698164
- StudyEvent: Eligibility
Similar models
Eligibility Menopausal Syndrome NCT01698164
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Amenorrhea Duration
Item
going through amenorrhea above 6 months and within 5 years,
boolean
C0002453 (UMLS CUI [1,1])
C0449238 (UMLS CUI [1,2])
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])
Uterine Fibroid Diameter
Item
uterine fibroid diameter≥5cm,
boolean
C0042133 (UMLS CUI [1,1])
C1301886 (UMLS CUI [1,2])
C1301886 (UMLS CUI [1,2])
Diabetes Mellitus | Hypertensive disease
Item
history of diabetes or hypertension,
boolean
C0011849 (UMLS CUI [1])
C0020538 (UMLS CUI [2])
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])
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])
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])
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])
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])