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Invest-CTO PCI Trial

Active, not recruitingNot applicableNCT04774913
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

This study has no listed site in Canada in this snapshot. It is included as part of the worldwide chronic pain corpus.

Brief summary (from the registry)

Following unsuccessful CTO crossing a CTO modification procedure is sometimes performed. CTO PCI registries where plaque modification has been performed in some patients, report this to be safe, and associated with higher success rates at subsequent attempts. It has never been investigated whether a planned investment procedure, with an intention that both the initial and staged completion PCI are of shorter duration, could improve safety and efficacy. The investigators hypothesize that 1. A planned investment procedure in the treatment of CTOs will be associated with improved patient safety 2. A planned investment procedure will be associated with improved cumulative procedure success rates 3. A planned two stage procedure will be associated with improved patient experience

Study details

Official title
Invest-CTO: Effectiveness and Safety of a Planned Investment Procedure in High-Risk CTO PCI
Conditions
Interventions
  • Procedure: Chronic total occlusion(CTO) percutaneous coronary intervention (PCI)
Sponsor
Haukeland University Hospital
Collaborators
Golden Jubilee National Hospital
Start date
2021-12-08
Primary completion
2025-10-09
Sex
All
Age range
from 18 Years
Results posted
No results posted in this snapshot
Countries
Norway, United Kingdom, United States
Total sites listed
5

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Ability to provide written informed consent * Comply with the procedural and study follow-up schedule * Planned CTO PCI in accordance with the European and American appropriateness criteria. * CTO defined as high-risk Exclusion Criteria: * Non-high risk CTO * Occlusion within a stent * Flush aorto-ostial occlusion of RCA and Left Main (LMS) * Limited arterial access precluding repeat procedure * Baseline non invasive testing showing non-viable target vessel territory * Contra-indication to dual antiplatelet therapy * Pregnancy * Prior radiation skin injury * Lack of informed consent

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT04774913