Stenting in Coarctation of Aorta (CoA)
Not Applicable
Recruiting
- Conditions
- Coarctation ofaorta.Coarctation of aorta
- Registration Number
- IRCT20181022041406N3
- Lead Sponsor
- Rajaie cardiovascular medical and research center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 100
Inclusion Criteria
All patients with native Corctation of aorta referred to rajaie cardiovascular medical and research center for stenting
Exclusion Criteria
Patients with noncircular aortic arch
Patients with preductal coarctation
Patients with hypoplastic aortic arch
Patients with right aberrant subclavian artery
Patients with stenosis more than 20 mm in length
Patients having aneurysm along with coarctation
Patients with common femoral artery and external iliac artery less than 7 mm in diameter
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Stent migration. Timepoint: During the procedure. Method of measurement: Fluoroscopy.;Aortic perforation. Timepoint: During the procedure. Method of measurement: Angiography.;Procedural success rate. Timepoint: Just after the procedure. Method of measurement: Catheterization.;Access site complication. Timepoint: Just after the procedure. Method of measurement: CT angiography.;Recoarctation. Timepoint: 6 and 12 months after the intervention. Method of measurement: Catheterization.
- Secondary Outcome Measures
Name Time Method Mortality. Timepoint: During hospitalization. Method of measurement: Questionnaire.;Aneurysm formation. Timepoint: 12 months after intervention. Method of measurement: CT angiography.