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NCT06009757 · ClinicalTrials.gov record · last posted 2026-08-26

GUIDEX® Versus Launcher™ Guiding Catheter in Percutaneous Coronary Intervention (PCI) (GUIDEX_FR)

Study acronym: GUIDEX®_FR
StatusCompleted
PhaseNot applicable
Started2025-04-10
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from the ClinicalTrials.gov record
The goal of this clinical trial is to compare two guiding catheters in patients with coronary artery disease during a percutaneous coronary intervention between Guidex® Guiding catheter (DEMAX) and Launcher™ coronary guide catheters (Medtronic). The main question\[s\] it aims to answer are: * Aren't the safety of medical devices inferior to each other? * Aren't the efficacyof medical devices inferior to each other? Participants will be randomized (1:1) and have a percutaneous coronary interventionwith one of the two guiding catheters.

Protocol amendment history 4 changes detected by DataLookout

2026-08-27
Trial status changed: Unknown → Completed
2026-08-27
Primary completion pushed: 2024-09 → 2026-01-06
2026-08-27
Completion pushed: 2025-02 → 2026-01-06
2026-08-02
Trial status changed: Not Yet Recruiting → Unknown
Trial Details
NCT Number NCT06009757
Lead Sponsor Tianjin Demax Medical Technology Co., Ltd
Conditions Coronary Artery Disease
Enrollment 150 participants
Start Date 2025-04-10
Primary Completion 2026-01-06 (estimated)
Study Completion 2026-01-06 (estimated)
Updated on ClinicalTrials.gov 2026-08-26