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NCT06795763

Acolyte CTO-PCI Study: Imaging and Catheter System to Treat Patients With Coronary Chronic Total Occlusion, Who Have Persistent Symptoms Following Medical Therapy and Are Undergoing Percutaneous Coronary Interventional Procedures

ENROLLING BY INVITATION NA Last updated 23 February 2026
What this trial tests

NA trial testing CTO-PCI Procedure with Acolyte Catheter System in Coronary Chronic Total Occlusions in 115 participants. Enrolling by invitation.

Timeline
6 August 2025
Primary endpoint
1 September 2026
1 September 2027

Quick facts

Lead sponsorElumn8 Medical
PhaseNA
StatusENROLLING BY INVITATION
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment115
Start date6 August 2025
Primary completion1 September 2026
Estimated completion1 September 2027
Sites5 locations across United States

Drugs / interventions tested

Conditions studied

Sponsor

Elumn8 Medical

Who can join

18 and older, any sex, with Coronary Chronic Total Occlusions or Ischemic Heart Disease. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a study to evaluate the safety and effectiveness of the Acolyte Catheter System used in CTO-PCI procedures. The system will be used for the placement and positioning of guidewires and catheters in the coronary vasculature for the treatment of patients with coronary chronic total occlusions with persistent symptoms following medical therapy.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Coronary Chronic Total Occlusions

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06795763.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing