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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01841346
Other study ID # JoPCR1-12-12-12
Secondary ID
Status Completed
Phase N/A
First received April 24, 2013
Last updated January 7, 2017
Start date March 2013
Est. completion date February 2015

Study information

Verified date January 2017
Source Jordan Collaborating Cardiology Group
Contact n/a
Is FDA regulated No
Health authority Jordan: Ethical Committee
Study type Observational [Patient Registry]

Clinical Trial Summary

The investigators will look at the short- (in hospital) and long- term ( 1 year)outcome in consecutive patients who undergo stent implantation and angioplasty in Jordan.


Description:

1. Voluntary registry of consecutive patients undergoing Percutaneous coronary intervention (PCI).

2. Patients will be treated according to the treating cardiologists' discretion. No randomization of any medication or stent.

3. Baseline data on admission will be collected (cardiovascular risk factors, blood lipids, ect).

4. PCI procedure details and complications will be documented during the index admission.

5. Outcome events (death, MI, revascularization, stent thrombosis) will be evaluated at 1, 6, and 12 months by clinic visits or phone calls.


Recruitment information / eligibility

Status Completed
Enrollment 2000
Est. completion date February 2015
Est. primary completion date February 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years to 100 Years
Eligibility Inclusion Criteria:

- Consecutive PCI patients

- Arab nationality

Exclusion Criteria:

- less than 18 year of age

Study Design

Observational Model: Case-Only, Time Perspective: Prospective


Related Conditions & MeSH terms

  • Percutaneous Coronary Intervention

Intervention

Procedure:
Procedure: PCI


Locations

Country Name City State
Jordan Istishari Hospital Amman

Sponsors (2)

Lead Sponsor Collaborator
Jordan Collaborating Cardiology Group AstraZeneca

Country where clinical trial is conducted

Jordan, 

Outcome

Type Measure Description Time frame Safety issue
Other Stent thrombosis All cases of definite/probable/possible stent thrombosis will be documented from the time of stent implantation during the index admission to 1 year. 1 year No
Other Baseline risk factors and outcome after 1 year Several factors at baseline will be evaluated as potential contributors to adverse outcome after one year, including: age, gender, renal impairment, heart failure, CRUSADE bleeding risc score, GRACE risk score, diabetes, multiple risk factors, BMI, and smoking. 1 year No
Other Adherence to guidelines in patients undergoing PCI Using medications (statins, antiplatelets, ACI inhibitors/ARBs, B blockers, etc),and diagnostic and interventional procedures, and reaching target parameters (LDL cholesterol and HbA1c) according to the published guidelines will be evaluated. 1 year No
Primary Cardiovascular mortality All cases of deaths from cardiovascular causes will be counted at 1 year. 1 year No
Secondary Admission for urgent coronary revascularization All events of hospital readmission for repeat coronary intervention for acute coronary syndrome from the time of discharge from hospital up to 1 year will be documented. 1 year No
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