Clinical Trials Logo
  1. Home
  2. Coronary Occlusion
  3. NCT03159650

Comparative Study Between Intravascular Ultrasonography Guided and Angiography-guided Recanalization of Coronary Chronic Total Occlusions

Coronary Occlusion Clinical Trial

Official title:
Randomized Comparative Study Between Intravascular Ultrasonography Guided and Angiography-guided Recanalization of Coronary Chronic Total Occlusions

Clinical Trial Summary

Chronic total occlusion is defined as thrombolysis in myocardial infarction (TIMI) flow grade 0 with an estimated duration of at least 3 months. The interest in chronic total occlusion (CTO) percutaneous coronary intervention (PCI) has increased, but with failure rate up to 20%, leading to important developments in dedicated equipment and techniques.

In the 2014 European Guidelines on Myocardial Revascularization, intravascular ultrasound was recommended to guide stent implantation in selected patients, and this recommendation was a class IIa/level of evidence B.

In CTO PCI, certain angiographic features such as blunt proximal CTO cap, tortuosity, heavy calcification, and lack of visibility of path in the distal vessel increase procedural difficulty

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03159650
Study type Interventional
Source Assiut University
Contact Hosam Hasan, professor
Phone +20882361015
Email hosam_hasan@hotmail.com
Status Not yet recruiting
Phase N/A
Start date June 1, 2017
Completion date October 1, 2019
View Details
See also
  Status Clinical Trial Phase
Completed NCT01721096 - XIENCE PRIME Japan Post-Marketing Surveillance (PMS)
Completed NCT00987610 - Guidewire for Chronic Total Occlusion Phase 4
Completed NCT02533128 - Biomarkers, Blood Pressure, BIS: Risk Stratification/Management of Patients at Cardiac Risk in Major Noncardiac Surgery N/A
Completed NCT04246125 - Patient Skin Dose in Interventional Radiology
Completed NCT03717675 - Supplemental Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter N/A
Recruiting NCT03588481 - IRIS- DESyne X2 in the IRIS-DES Registry
Recruiting NCT05089864 - STAR and Deferred Stenting Study N/A
Not yet recruiting NCT03719014 - Cohort B of the Pivotal Study to Evaluate the Safety and Effectiveness of the NovaCross™ Micro-catheter N/A
Not yet recruiting NCT02963584 - Decision Aid in Chronic Total Occlusion (CTO) Patients N/A
Completed NCT00793221 - Non-acute Coronary occlusIon Treated By Everolimus ELuting Stent Phase 3
Completed NCT04281212 - Observational Study Evaluating the Management of Chronic Coronary Occlusions In France
Not yet recruiting NCT04562142 - A Novel Non-Invasive Acoustic Diagnostic for the Diagnosis of Coronary Artery Disease The CAD-det Validation Study N/A
Enrolling by invitation NCT02931331 - Coronary Revascularization Assessed by Stress PET N/A
Terminated NCT02683356 - Optical Coherence Tomography to Improve Outcome for Coronary Revascularisation Using Bioresorbable Vascular Scaffolds N/A
Completed NCT00657436 - Myeloid-Related Protein in Evaluation of Acute Chest Pain in the Emergency Departement N/A
Not yet recruiting NCT05848232 - Single-Arm Study Evaluating Use of the CORA Catheters for the Crossing of Coronary Chronic Total Occlusions Phase 3
Terminated NCT03993522 - Exercise in Patients With a Total Coronary Occlusion N/A
Recruiting NCT02325869 - Clinical Study Protocol - Debris Interventional Removal in ACS (DESIRE-ACS) N/A
Completed NCT00640068 - Advanced Cardiovascular Imaging Consortium N/A
Completed NCT01759290 - ABSORB FIRST is a Registry Designed to Evaluate the Safety and Performance of Absorb Bioresorbable Vascular Scaffold (Absorb BVS) Used in Real-world Patients. N/A