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NCT06682910 · ClinicalTrials.gov record · last posted 2026-08-21

Assessment of Safety and Accuracy of the Microtech System in Patients Undergoing Left Ventricular Assist Device Implantation

Study acronym: Microtech-LVAD
StatusActive, Not Recruiting
PhaseNot applicable
Started2024-12-15
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from the ClinicalTrials.gov record
The Microtech-LVAD study is designed as a prospective, single arm, multi-center early feasibility study. Approximately 15 patients will be enrolled in the study. The study will be limited to patients in whom it is decided, based on routine clinical practice, that the LVAD will be implanted via a midline sternotomy. In the first 5 study patients, the device will be implanted in the RA; subsequently, the device will be implanted in the LA unless the patient is deemed at high risk of post-LVAD right heart failure, in which case the device will be placed in the RA

Protocol amendment history 3 changes detected by DataLookout

2026-08-22
Enrollment closed, study ongoing
2026-08-22
Primary completion pushed: 2026-05 → 2026-11
2026-08-22
Completion pushed: 2026-11 → 2027-12
Trial Details
NCT Number NCT06682910
Lead Sponsor Microtech Medical Technologies, Ltd
Conditions Heart Failure
Enrollment 15 participants
Start Date 2024-12-15
Primary Completion 2026-11 (estimated)
Study Completion 2027-12 (estimated)
Updated on ClinicalTrials.gov 2026-08-21