Informações:
Falhas:
ID
34085
Descrição
Modified Relaxation (MR) Technique for Treating Hypertension in Postmenopausal Women; ODM derived from: https://clinicaltrials.gov/show/NCT01429662
Link
https://clinicaltrials.gov/show/NCT01429662
Palavras-chave
Versões (1)
- 14-01-19 14-01-19 -
Titular dos direitos
See clinicaltrials.gov
Transferido a
14 januari 2019
DOI
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Licença
Creative Commons BY 4.0
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Eligibility Postmenopausal Syndrome NCT01429662
Eligibility Postmenopausal Syndrome NCT01429662
- StudyEvent: Eligibility
Similar models
Eligibility Postmenopausal Syndrome NCT01429662
- StudyEvent: Eligibility
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de dados
Alias
Essential Hypertension Stage | Systolic Pressure Measurement Quantity | Diastolic blood pressure Measurement Quantity
Item
stage 1 essential hypertension, defined as a systolic blood pressure of 140-159 and/or dbp of 90-99 mmhg on two occasions at least 30 minutes apart.
boolean
C0085580 (UMLS CUI [1,1])
C1306673 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0242485 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0428883 (UMLS CUI [3,1])
C0242485 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
C1306673 (UMLS CUI [1,2])
C0871470 (UMLS CUI [2,1])
C0242485 (UMLS CUI [2,2])
C1265611 (UMLS CUI [2,3])
C0428883 (UMLS CUI [3,1])
C0242485 (UMLS CUI [3,2])
C1265611 (UMLS CUI [3,3])
Gender | Follow-up visit Able
Item
women who are able to attend follow visits as advised.
boolean
C0079399 (UMLS CUI [1])
C0589121 (UMLS CUI [2,1])
C0085732 (UMLS CUI [2,2])
C0589121 (UMLS CUI [2,1])
C0085732 (UMLS CUI [2,2])
Gender | Systolic Pressure | Diastolic blood pressure
Item
women with systolic blood pressure (sbp) >160 mmhg or diastolic blood pressure (dbp) >100 mmhg.
boolean
C0079399 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Gender | Etiology Hypertensive disease | Kidney Diseases
Item
women who have other known causes of hypertension, such as renal diseases
boolean
C0079399 (UMLS CUI [1])
C0015127 (UMLS CUI [2,1])
C0020538 (UMLS CUI [2,2])
C0022658 (UMLS CUI [3])
C0015127 (UMLS CUI [2,1])
C0020538 (UMLS CUI [2,2])
C0022658 (UMLS CUI [3])
Gender | Sedatives | Tranquilizing Agents | Antidepressive Agents | Antihypertensive Agents
Item
women who are using sedatives or tranquilizer,or antidepressant, or antihypertensive medication during the past 2 months prior to the study.
boolean
C0079399 (UMLS CUI [1])
C0036557 (UMLS CUI [2])
C0040614 (UMLS CUI [3])
C0003289 (UMLS CUI [4])
C0003364 (UMLS CUI [5])
C0036557 (UMLS CUI [2])
C0040614 (UMLS CUI [3])
C0003289 (UMLS CUI [4])
C0003364 (UMLS CUI [5])
Language Barrier | Problem Geographic
Item
have language or geographical barrier.
boolean
C0237167 (UMLS CUI [1])
C0033213 (UMLS CUI [2,1])
C1517526 (UMLS CUI [2,2])
C0033213 (UMLS CUI [2,1])
C1517526 (UMLS CUI [2,2])
Informed Consent Lacking
Item
do not give their informed consent.
boolean
C0021430 (UMLS CUI [1,1])
C0332268 (UMLS CUI [1,2])
C0332268 (UMLS CUI [1,2])
Gender | Patient need for Hormone replacement therapy
Item
women who need to be prescribed hrt.
boolean
C0079399 (UMLS CUI [1])
C0686904 (UMLS CUI [2,1])
C0282402 (UMLS CUI [2,2])
C0686904 (UMLS CUI [2,1])
C0282402 (UMLS CUI [2,2])