EchoTip AcuCore Post-Market Clinical Study

NCT06358001 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 183

Last updated 2025-09-22

No results posted yet for this 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

Interventions

DEVICE

EchoTip AcuCore

Using endoscopic ultrasound guided needle to collect biopsies

Sponsors & Collaborators

  • Cook Research Incorporated

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-08-05
Primary Completion
2025-06-14
Completion
2025-07-19

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06358001 on ClinicalTrials.gov