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NCT06682910 · ClinicalTrials.gov registry record · NA

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

A NA study of Heart Failure, sponsored by Microtech Medical Technologies.

Recruiting
Registry status
NA
Development phase
15
Enrollment target
2
Study locations

NCT06682910: Recruiting NA study of Heart Failure, sponsored by Microtech Medical Technologies.

NCT06682910 is a NA study of Heart Failure that is actively recruiting participants, run by Microtech Medical Technologies. The registered enrollment target is 15 participants, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (99% lower). The trial reports 2 study locations across 2 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06682910, a NA study of Heart Failure, is actively recruiting participants, sponsored by Microtech Medical Technologies.

RECRUITING
Registry status
NA
Development phase
15 participants
Enrollment target
2
Study locations

Study Summary

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

Conditions Studied

Interventions

  • DEVICE Microtech sensor pressure

Study Locations (2)

New York

  • Columbia University Medical Center/ NewYork Presbyterian Hospital or CUMC/NYPH - New York

Other

  • Rabin Medical Center - Petach Tikvah

Trial Details

FieldValue
Enrollment Target 15 participants
Start Date 2024-12-15
Est. Completion 2026-11
Phase NA

Sponsor

Microtech Medical Technologies

1 total trials

What the Registry Record Tells You About NCT06682910

The ClinicalTrials.gov registry entry for NCT06682910 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 15 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,049-participant average among 397 other Heart Failure trials with a reported enrollment target (99% lower). The listed sponsor is Microtech Medical Technologies, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Heart Failure appearing as the primary indexed condition, and to 1 intervention - of which Microtech sensor pressure is the first listed.

NCT06682910 reports 2 study locations spanning 2 distinct geographic areas - top geographies include New York, Other.

Frequently Asked Questions

What is clinical trial NCT06682910 about?

NCT06682910 is a clinical study titled "Assessment of Safety and Accuracy of the Microtech System in Patients Undergoing Left Ventricular Assist Device Implantation". 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 mid...

What is the current status of trial NCT06682910?

This trial is currently recruiting. It is a NA study. The enrollment target is 15 participants. The study started on 2024-12-15. Estimated completion is 2026-11.

What conditions does trial NCT06682910 study?

This clinical trial studies the following conditions: Heart Failure.

What interventions are being tested in trial NCT06682910?

The interventions under investigation include: Microtech sensor pressure (DEVICE).

Who is sponsoring clinical trial NCT06682910?

This trial is sponsored by Microtech Medical Technologies, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06682910 being conducted?

This trial has 2 study locations across New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, the data changelog, or report a data error.