# COmplex BifuRcation Lesions: a Comparison Between the AXXESS Device and Culotte Stenting: an Optical Coherence Tomography (OCT) Study

> **NCT01486095** · NA · UNKNOWN · sponsor: **Universitaire Ziekenhuizen KU Leuven** · enrollment: 40 (estimated)

## Conditions studied

- True Coronary Bifurcation Lesions

## Interventions

- **DEVICE:** AXXESS + Biomatrix Biolimus Eluting stent
- **DEVICE:** Culotte technique with Xience V or Xience Prime stents

## Key facts

- **NCT ID:** NCT01486095
- **Lead sponsor:** Universitaire Ziekenhuizen KU Leuven
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** UNKNOWN
- **Start date:** 2011-11-29
- **Primary completion:** 2013-12
- **Final completion:** 2017-12
- **Target enrollment:** 40 (ESTIMATED)
- **Last updated:** 2017-05-09

## Collaborators

- [object Object]

## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT01486095

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT01486095, "COmplex BifuRcation Lesions: a Comparison Between the AXXESS Device and Culotte Stenting: an Optical Coherence Tomography (OCT) Study". Retrieved via AI Analytics 2026-06-02 from https://api.ai-analytics.org/clinical/NCT01486095. Licensed CC0.

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