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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ChiCTR
Last refreshed on: 24 July 2017
Main ID:  ChiCTR-RRC-17012095
Date of registration: 2017-07-23
Prospective Registration: Yes
Primary sponsor: The Eighth Hospital of Qingdao
Public title: Association of contrast dosage and slow-flow or no-reflow phenomenon after percutaneous transluminal coronary angioplasty and stent for patients with non-ST-segment elevation acute coronary syndrome-a case control study
Scientific title: Association of contrast dosage and slow-flow or no-reflow phenomenon after percutaneous transluminal coronary angioplasty and stent for patients with non-ST-segment elevation acute coronary syndrome-a case control study
Date of first enrolment: 2017-08-01
Target sample size: case group:120;control group:120;
Recruitment status: Recruiting
URL:  http://www.chictr.org.cn/showproj.aspx?proj=20530
Study type:  Relative factors research
Study design:  Case-Control study  
Phase:  Retrospective study
Countries of recruitment
China
Contacts
Name: Sihua Ding   
Address:  84 Fengshan Road, Qingdao, Shandong, China 266100
Telephone: +86 13964830753
Email: dsh1226@163.com
Affiliation:  The Eighth Hospital of Qingdao
Name: Sihua Ding   
Address:  84 Fengshan Road, Qingdao, Shandong, China 266100
Telephone: +86 13964830753
Email: dsh1226@163.com
Affiliation:  The Eighth Hospital of Qingdao
Key inclusion & exclusion criteria
Inclusion criteria: Patients with the diagnosis of non-ST segment elevation acute coronary syndrome receiving percutaneous coronary intervention after being hospitalized.
Exclusion criteria: 1. Patients with coronary artery stent stenosis receiving percutaneous transluminal coronary angioplasty and stent;
2. Patients with bridge blood vessel receiving percutaneous transluminal coronary angioplasty and stent;
3. Patients receiving coronary rotablation.


Age minimum: 30
Age maximum: 100
Gender: Both
Health Condition(s) or Problem(s) studied
ICD-10:I20.0/20.1/20.9,ICD-10:I21.4
non-ST-segment elevation acute coronary syndrome
Intervention(s)
case group:none;control group:none;
Primary Outcome(s)
contrast dosage;TIMI grade of coronary blood flow;
Secondary Outcome(s)
Secondary ID(s)
Source(s) of Monetary Support
The Qingdao municipal health and family planning commission
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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