Status:

RECRUITING

Use of Physiology to Evaluate Procedural Result After PCI CTO

Lead Sponsor:

Isala

Collaborating Sponsors:

Abbott

Conditions:

Percutaneous Coronary Revascularisation

Complex Coronary Lesion

Eligibility:

All Genders

18+ years

Phase:

NA

Brief Summary

ULTRA-CTO is a prospective multicentre non-randomised investigator-initiated trial designed to enrol 200 subjects with an indication for percutaneous coronary intervention (PCI) of chronic total occlu...

Detailed Description

ULTRA-CTO is a prospective multicentre non-randomised investigator-initiated trial designed to enrol 200 subjects with an indication for PCI CTO. The main objective of the study is to evaluate both t...

Eligibility Criteria

Inclusion

  • Age 18 years and older.
  • Angiographically successful PCI CTO without any remaining lesion at least 30% proximal to the stented segment.
  • Possibility to perform physiologic measurements and OCT of sufficient quality.
  • Patients willing and capable to provide written informed consent.

Exclusion

  • 1\) Contra-indication for adenosine.

Key Trial Info

Start Date :

July 21 2021

Trial Type :

INTERVENTIONAL

Allocation :

ESTIMATED

End Date :

June 1 2026

Estimated Enrollment :

200 Patients enrolled

Trial Details

Trial ID

NCT04780971

Start Date

July 21 2021

End Date

June 1 2026

Last Update

February 19 2025

Active Locations (2)

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Page 1 of 1 (2 locations)

1

Radboud UMC

Nijmegen, Netherlands

2

Isala

Zwolle, Netherlands, 8025 AB

Use of Physiology to Evaluate Procedural Result After PCI CTO | DecenTrialz