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Chronic Total Coronary Occlusion Treatment Results 6 Years After Bioresorbable Scaffold Implantation

NCT06164977 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 34

Last updated 2025-06-11

No results posted yet for this study

Summary

Aim of the study is to evaluate chronic total coronary occlusion treatment results 6 years after bioresorbable scaffold implantation by quantitative coronary analysis, intravascular ultrasound and optical coherence tomography.

Conditions

Interventions

PROCEDURE

Percutaneous coronary intervention.

Revascularization of chronic total coronary occlusion.

Sponsors & Collaborators

  • Pauls Stradins Clinical University Hospital

    lead OTHER

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-02-01
Primary Completion
2023-12-01
Completion
2023-12-01

Countries

  • Latvia

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06164977 on ClinicalTrials.gov