Informatie:
Fout:
ID
40314
Beschrijving
Galectin-3 Blockade in Patients With High Blood Pressure; ODM derived from: https://clinicaltrials.gov/show/NCT01960946
Link
https://clinicaltrials.gov/show/NCT01960946
Trefwoorden
Versies (1)
- 06-04-20 06-04-20 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
6 april 2020
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 Hypertension NCT01960946
Eligibility Hypertension NCT01960946
- StudyEvent: Eligibility
Similar models
Eligibility Hypertension NCT01960946
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
age 21-70 years
boolean
C0001779 (UMLS CUI [1])
Hypertensive disease | Therapeutic procedure Stable
Item
physician diagnosed hypertension on stable therapy for 3 months
boolean
C0020538 (UMLS CUI [1])
C0087111 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
C0087111 (UMLS CUI [2,1])
C0205360 (UMLS CUI [2,2])
Galectin-3 increased
Item
elevated galectin-3 level (above sex-specific median based on framingham heart study measures)
boolean
C4049292 (UMLS CUI [1])
Comprehension Study Protocol English Language | Informed Consent English Language
Item
able to understand the protocol and provide informed consent in english
boolean
C0162340 (UMLS CUI [1,1])
C2348563 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
C2348563 (UMLS CUI [1,2])
C0376245 (UMLS CUI [1,3])
C0021430 (UMLS CUI [2,1])
C0376245 (UMLS CUI [2,2])
Uncontrolled hypertension | Systolic Pressure | Diastolic blood pressure
Item
uncontrolled hypertension, defined as systolic blood pressure > 170mmhg, diastolic blood pressure > 100mmhg
boolean
C1868885 (UMLS CUI [1])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
Secondary hypertension
Item
evidence of secondary hypertension
boolean
C0155616 (UMLS CUI [1])
Heart failure | Coronary Artery Disease | Cerebrovascular accident | Atrial Fibrillation
Item
history of heart failure, coronary artery disease, stroke, atrial fibrillation
boolean
C0018801 (UMLS CUI [1])
C1956346 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0004238 (UMLS CUI [4])
C1956346 (UMLS CUI [2])
C0038454 (UMLS CUI [3])
C0004238 (UMLS CUI [4])
Left ventricular ejection fraction Echocardiography
Item
left ventricular ejection fraction < 45% on echocardiography
boolean
C0428772 (UMLS CUI [1,1])
C0013516 (UMLS CUI [1,2])
C0013516 (UMLS CUI [1,2])
Aldosterone Antagonists
Item
use of aldosterone antagonists
boolean
C0002007 (UMLS CUI [1])
Liver Cirrhosis
Item
history of liver cirrhosis
boolean
C0023890 (UMLS CUI [1])
Pulmonary Fibrosis
Item
history of pulmonary fibrosis
boolean
C0034069 (UMLS CUI [1])
Abnormal renal function | Estimated Glomerular Filtration Rate
Item
kidney dysfunction, defined as estimated glomerular filtration rate < 45 ml/min/1.73m2
boolean
C0151746 (UMLS CUI [1])
C3811844 (UMLS CUI [2])
C3811844 (UMLS CUI [2])
Anemia | Hematocrit procedure | Gender
Item
anemia, defined as hematocrit < 38% in men and < 36% in women
boolean
C0002871 (UMLS CUI [1])
C0018935 (UMLS CUI [2])
C0079399 (UMLS CUI [3])
C0018935 (UMLS CUI [2])
C0079399 (UMLS CUI [3])
Chelating Agents
Item
use of chelating agents
boolean
C0007974 (UMLS CUI [1])
Malignant Neoplasms
Item
history of cancer or malignancy
boolean
C0006826 (UMLS CUI [1])
Pregnancy | Gender Contraceptive methods Unwilling | Breast Feeding
Item
known pregnancy, those unwilling to avoid pregnancy during the course of the study, or women currently breastfeeding
boolean
C0032961 (UMLS CUI [1])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C0006147 (UMLS CUI [3])
C0079399 (UMLS CUI [2,1])
C0700589 (UMLS CUI [2,2])
C0558080 (UMLS CUI [2,3])
C0006147 (UMLS CUI [3])
Hyperkalemia | Potassium measurement
Item
hyperkalemia on screening labs, defined as potassium >5.0
boolean
C0020461 (UMLS CUI [1])
C0202194 (UMLS CUI [2])
C0202194 (UMLS CUI [2])
Completion of clinical trial Unable | Protocol Compliance Unable
Item
anticipated inability to complete or comply with study protocol
boolean
C2732579 (UMLS CUI [1,1])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
C1299582 (UMLS CUI [1,2])
C0525058 (UMLS CUI [2,1])
C1299582 (UMLS CUI [2,2])
Angioedema
Item
history of angioedema
boolean
C0002994 (UMLS CUI [1])