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NCT06164977Completed

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

Source: ClinicalTrials.gov · Last updated 11 Jun 2025

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Interventional
Enrollment
34 (actual)
First submitted
22 Nov 2023
Start date
1 Feb 2017
Primary completion date
1 Dec 2023
Lead sponsor
Pauls Stradins Clinical University Hospital
NCT number
NCT06164977

What you commit to

  • Study type: Interventional
  • Participants enrolled: 34
  • From 1 Feb 2017 to the primary completion date, 1 Dec 2023
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Participant withdrawal from study.

Who the study is looking for

  • 100% occlusion of a coronary artery for a duration of greater than or equal to 3 months based on angiographic evidence.

Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Pauls Stradins Clinical University Hospital
Coordinator of this site? Confirm its status
RigaLatviaUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.