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NCT06445504 · ClinicalTrials.gov registry record · NA

Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable Hernia Repair)

A NA study of Ventral Hernia and Inguinal Hernia, sponsored by Medtronic - MITG.

Active
Registry status
NA
Development phase
193
Enrollment target
7
Study locations

NCT06445504 is a NA study of Ventral Hernia and Inguinal Hernia that is active but no longer recruiting, run by Medtronic - MITG. The registered enrollment target is 193 participants, above the 132-participant average among 18 other Ventral Hernia trials with a reported enrollment target (46% higher). The trial reports 7 study locations across 7 states.

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The verdict

NCT06445504, a NA study of Ventral Hernia and Inguinal Hernia, is active but no longer recruiting, sponsored by Medtronic - MITG.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
193 participants
Enrollment target
7
Study locations

Study Summary

A prospective, multicenter, single-arm pivotal study will be performed with 192 subjects enrolled to have an inguinal or ventral robotic hernia repair procedure using the Medtronic Hugo™ RAS system. Subjects will be followed through two years. This study will be conducted using up to ten investigative sites in the United States (US).

Conditions Studied

Ventral Hernia Inguinal Hernia

Interventions

  • DEVICE Robotic-Assisted Surgery (RAS) Hernia Repair Surgery

Study Locations (7)

Florida

  • Tampa General Hospital - Tampa

Illinois

  • University of Illinois, Chicago - Chicago

New York

  • University of Buffalo - Buffalo

North Carolina

  • Duke University - Durham

Ohio

  • Cleveland Clinic - Cleveland

Texas

  • UT Health - Houston

Virginia

  • Bon Secours - Newport News

Trial Details

FieldValue
Enrollment Target 193 participants
Start Date 2024-04-08
Est. Completion 2027-03-15
Phase NA

Sponsor

Medtronic - MITG

119 total trials

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What the Registry Record Tells You About NCT06445504

The ClinicalTrials.gov registry entry for NCT06445504 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 193 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 132-participant average among 18 other Ventral Hernia trials with a reported enrollment target (46% higher). The listed sponsor is Medtronic - MITG, which has 119 total studies on file at ClinicalTrials.gov.

The record links to 2 conditions, with Ventral Hernia appearing as the primary indexed condition, and to 1 intervention - of which Robotic-Assisted Surgery (RAS) Hernia Repair Surgery is the first listed.

NCT06445504 reports 7 study locations spanning 7 distinct geographic areas - top geographies include Florida, Illinois, New York.

Frequently Asked Questions

What is clinical trial NCT06445504 about?

NCT06445504 is a clinical study titled "Medtronic Hugo™ Robotic Assisted Surgery (RAS) System in Hernia Surgery (Enable Hernia Repair)". A prospective, multicenter, single-arm pivotal study will be performed with 192 subjects enrolled to have an inguinal or ventral robotic hernia repair procedure using the Medtronic Hugo™ RAS system. Subjects will be followed through two years. This study will be conducted using up to ten investigati...

What is the current status of trial NCT06445504?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 193 participants. The study started on 2024-04-08. Estimated completion is 2027-03-15.

What conditions does trial NCT06445504 study?

This clinical trial studies the following conditions: Ventral Hernia, Inguinal Hernia.

What interventions are being tested in trial NCT06445504?

The interventions under investigation include: Robotic-Assisted Surgery (RAS) Hernia Repair Surgery (DEVICE).

Who is sponsoring clinical trial NCT06445504?

This trial is sponsored by Medtronic - MITG, which has 119 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06445504 being conducted?

This trial has 7 study locations across Florida, Illinois, New York, North Carolina, Ohio. 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 Editorial

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, or report a data error.