Informatie:
Fout:
ID
28771
Beschrijving
Study of Herbal Formula Corresponding to Syndrome in Treating Post Percutaneous Coronary Intervention (PCI) Patients With Coronary Heart Disease (CHD); ODM derived from: https://clinicaltrials.gov/show/NCT00817024
Link
https://clinicaltrials.gov/show/NCT00817024
Trefwoorden
Versies (1)
- 03-02-18 03-02-18 -
Houder van rechten
See clinicaltrials.gov
Geüploaded op
3 februari 2018
DOI
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Licentie
Creative Commons BY 4.0
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Eligibility Coronary Heart Disease NCT00817024
Eligibility Coronary Heart Disease NCT00817024
- StudyEvent: Eligibility
Similar models
Eligibility Coronary Heart Disease NCT00817024
- StudyEvent: Eligibility
Name
Type
Description | Question | Decode (Coded Value)
Datatype
Alias
Age
Item
18-75 years old
boolean
C0001779 (UMLS CUI [1])
Coronary heart disease Coronary angiography
Item
clinical diagnosis of coronary heart disease (confirmed by coronary angiography)
boolean
C0010068 (UMLS CUI [1,1])
C0085532 (UMLS CUI [1,2])
C0085532 (UMLS CUI [1,2])
Interventional procedure Successful | PTCA | PCI
Item
successfully received interventional therapy (ptca or pci)
boolean
C0184661 (UMLS CUI [1,1])
C1272703 (UMLS CUI [1,2])
C2936173 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
C1272703 (UMLS CUI [1,2])
C2936173 (UMLS CUI [2])
C1532338 (UMLS CUI [3])
TCM Blood Stasis Syndrome
Item
belong to tcm blood-stasis syndrome
boolean
C0025124 (UMLS CUI [1,1])
C2986501 (UMLS CUI [1,2])
C2986501 (UMLS CUI [1,2])
Able to swallow Tablets
Item
must be able to swallow tablets
boolean
C2712086 (UMLS CUI [1,1])
C0039225 (UMLS CUI [1,2])
C0039225 (UMLS CUI [1,2])
Informed Consent
Item
able to give written informed consent
boolean
C0021430 (UMLS CUI [1])
Symptomatic congestive heart failure New York Heart Association Classification
Item
symptomatic congestive heart failure(new york heart association class iii-iv)
boolean
C0742758 (UMLS CUI [1,1])
C1275491 (UMLS CUI [1,2])
C1275491 (UMLS CUI [1,2])
Pregnancy | Breast Feeding
Item
females during pregnancy or lactation
boolean
C0032961 (UMLS CUI [1])
C0006147 (UMLS CUI [2])
C0006147 (UMLS CUI [2])
Dysfunction Serious Organ Important | Liver Dysfunction Serious | Dysfunction Serious Lung | Renal dysfunction Serious
Item
serious dysfunction in important organs (liver, lung, kidney，et al)
boolean
C3887504 (UMLS CUI [1,1])
C0205404 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,3])
C3898777 (UMLS CUI [1,4])
C0086565 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C3887504 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C0024109 (UMLS CUI [3,3])
C3279454 (UMLS CUI [4,1])
C0205404 (UMLS CUI [4,2])
C0205404 (UMLS CUI [1,2])
C0178784 (UMLS CUI [1,3])
C3898777 (UMLS CUI [1,4])
C0086565 (UMLS CUI [2,1])
C0205404 (UMLS CUI [2,2])
C3887504 (UMLS CUI [3,1])
C0205404 (UMLS CUI [3,2])
C0024109 (UMLS CUI [3,3])
C3279454 (UMLS CUI [4,1])
C0205404 (UMLS CUI [4,2])
Chinese herbal medicine
Item
use of concomitant chinese herbal medicine
boolean
C1273412 (UMLS CUI [1])
Study Subject Participation Status
Item
already attend other clinical trial
boolean
C2348568 (UMLS CUI [1])