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EchoTip AcuCore Post-Market Clinical Study
NCT06358001 · View on ClinicalTrials.gov ↗
Study Summary
The purpose of collecting this data is to continue to learn more about the EchoTip AcuCore and the device's ability to produce the desired favorable effect and if there are any undesired outcomes that may be related to the EchoTip AcuCore.
Conditions Studied
Interventions
- DEVICE EchoTip AcuCore
Study Locations (8)
Florida
- Shands Hospital-University of Florida — Gainesville
- University of Florida Shands Hospital — Gainesville
- Advent Health Medical Group, Orlando — Orlando
California
- University of California, Irvine — Orange
Colorado
- Advent Health, Porter — Denver
Pennsylvania
- Geisinger Medical Center — Danville
Texas
- University of Texas Memorial Hermann Hospital — Houston
Virginia
- University of Virginia — Charlottesville
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 183 participants |
| Start Date | 2024-08-05 |
| Est. Completion | 2025-07-19 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06358001
The ClinicalTrials.gov registry entry for NCT06358001 describes a study currently listed as completed. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 183 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Cook Research Incorporated, which has 6 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 8 conditions, with Hepatocellular Carcinoma appearing as the primary indexed condition, and to 1 intervention — of which EchoTip AcuCore is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT06358001 reports 8 study locations spanning 6 distinct geographic areas — top geographies include Florida, California, Colorado. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT06358001 about?
NCT06358001 is a clinical study titled "EchoTip AcuCore Post-Market Clinical Study". The purpose of collecting this data is to continue to learn more about the EchoTip AcuCore and the device's ability to produce the desired favorable effect and if there are any undesired outcomes that may be related to the EchoTip AcuCore.
What is the current status of trial NCT06358001?
This trial is currently completed. The enrollment target is 183 participants. The study started on 2024-08-05. Estimated completion is 2025-07-19.
What conditions does trial NCT06358001 study?
This clinical trial studies the following conditions: Hepatocellular Carcinoma, Cholangiocarcinoma, Neuroendocrine Tumors, Chronic Pancreatitis, Adenocarcinoma. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT06358001?
The interventions under investigation include: EchoTip AcuCore (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT06358001?
This trial is sponsored by Cook Research Incorporated, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT06358001 being conducted?
This trial has 8 study locations across California, Colorado, Florida, Pennsylvania, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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