2000 Participants NeededMy employer runs this trial

Chronic Total Occlusion Intervention for Coronary Artery Disease

(PROGRESS-CTO Trial)

Recruiting at 47 trial locations
ES
Overseen ByEmmanouil S Brilakis, MD, PhD
Age: Any Age
Sex: Any
Trial Phase: Academic
Sponsor: Minneapolis Heart Institute Foundation
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

Percutaneous coronary intervention (PCI) of chronic total occlusions (CTOs) is increasingly being performed in patients with advanced coronary artery disease, but there is limited information on the techniques utilized and the procedural outcomes. The goal of this multicenter, investigator initiated registry is to collect information on treatment strategies and outcomes of consecutive patients undergoing CTO PCI among various participating centers. The information collected will be used to determine the frequency of CTO PCI performed at the participating sites and examine the procedural strategies utilized, and the procedural (both immediate and during follow-up) outcomes.

Who Is on the Research Team?

ES

Emmanouil S Brilakis, MD, PhD

Principal Investigator

Minneapolis Heart Institute Foundation

Are You a Good Fit for This Trial?

Inclusion Criteria

Patients undergoing CTO PCI at each of the participating centers.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants undergo percutaneous coronary intervention (PCI) for chronic total occlusions (CTOs)

1 day
1 visit (in-person)

Follow-up

Participants are monitored for major adverse cardiovascular events (MACE) and procedural success after PCI

Variable, based on clinical need

What Are the Treatments Tested in This Trial?

Find a Clinic Near You

Who Is Running the Clinical Trial?

Minneapolis Heart Institute Foundation

Lead Sponsor

Trials
32
Recruited
15,700+