RECRUITING

Progress Bifurcation Global Registry

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Coronary bifurcation lesions are lesions (or blockages) that occur at or near the intersection of a major coronary artery and one of the arteries' side branches. Numerous techniques and devices have been developed to treat coronary bifurcations; however, these types of lesions remain some of the most challenging, both in terms of procedural success and outcome. This study is designed as an observational, multi-center registry that will collect information on treatment strategies and outcomes of consecutive patients undergoing percutaneous coronary interventions (PCI) in coronary bifurcations among various participating centers, in order to determine the frequency of bifurcation PCI, the procedural strategies utilized, and the procedural outcomes.

Official Title

Prospective Global Registry of Percutaneous Coronary Intervention in Bifurcation Lesions (PROGRESS-BIFURCATION)

Quick Facts

Study Start:2020-04-23
Study Completion:2030-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05100992

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:Not specified
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Over 18 years of age
  2. * undergoing bifurcation percutaneous coronary intervention
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Contact

Emmanouil Brilakis, MD, PhD
CONTACT
612-863-3852
emmanouil.brilakis@allina.com
Bavana Rangan, BDS, MPH
CONTACT
612-863-3852
bavana.rangan@allina.com

Study Locations (Sites)

Minneapolis Heart Institute Foundation
Minneapolis, Minnesota, 55407
United States

Collaborators and Investigators

Sponsor: Minneapolis Heart Institute Foundation

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2020-04-23
Study Completion Date2030-01

Study Record Updates

Study Start Date2020-04-23
Study Completion Date2030-01

Terms related to this study

Keywords Provided by Researchers

  • bifurcation lesions
  • percutaneous coronary intervention

Additional Relevant MeSH Terms

  • Coronary Artery Disease
  • Coronary Bifurcation Lesions