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ACTIVE NOT RECRUITING NA

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

NCT06445504 · View on ClinicalTrials.gov ↗

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).

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

89 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06445504

The ClinicalTrials.gov registry entry for NCT06445504 describes a study currently listed as active not recruiting. It is categorized as NA, 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 193 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic - MITG, which has 89 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. 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: NCT06445504 reports 7 study locations spanning 7 distinct geographic areas — top geographies include Florida, Illinois, New York. 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 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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06445504?

The interventions under investigation include: Robotic-Assisted Surgery (RAS) Hernia Repair Surgery (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06445504?

This trial is sponsored by Medtronic - MITG, which has 89 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial