Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING NA

Chronic Nausea and Vomiting in Patients With Normal Gastric Emptying Using the Enterra® Therapy System (NAVIGATE)

NCT06464926 · View on ClinicalTrials.gov ↗

Study Summary

The purpose of this research study is to determine if the Enterra® Therapy System can decrease nausea and vomiting symptoms and improve the quality of life for patients with chronic nausea, with or without vomiting, that have normal gastric emptying.

Conditions Studied

Interventions

  • DEVICE Enterra Therapy System

Study Locations (17)

Other

  • UZ Leuven — Leuven
  • Hôpital Louis-Mourier — Colombes
  • Hôpital Edouard Herriot - CHU de Lyon — Lyon
  • CHU de Bordeaux — Pessac
  • CHU de Rouen — Rouen
  • Sahlgrenska Universitetssjukhuset — Gothenburg

California

  • Hoag Hospital — Newport Beach
  • Sutter Health — San Francisco

Arizona

  • Mayo Clinic Arizona — Scottsdale

Florida

  • University of South Florida — Tampa

Illinois

  • Endeavor Health — Evanston

Indiana

  • Indiana University Health — Indianapolis

Kentucky

  • University of Louisville — Louisville

New Jersey

  • Hackensack Meridian — Neptune City

Trial Details

FieldValue
Enrollment Target 148 participants
Start Date 2025-06-23
Est. Completion 2030-06
Phase NA

Sponsor

Enterra Medical

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06464926

The ClinicalTrials.gov registry entry for NCT06464926 describes a study currently listed as 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 148 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Enterra Medical, which has 3 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 Nausea appearing as the primary indexed condition, and to 1 intervention — of which Enterra Therapy System 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: NCT06464926 reports 17 study locations spanning 11 distinct geographic areas — top geographies include Other, California, Arizona. 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 NCT06464926 about?

NCT06464926 is a clinical study titled "Chronic Nausea and Vomiting in Patients With Normal Gastric Emptying Using the Enterra® Therapy System (NAVIGATE)". The purpose of this research study is to determine if the Enterra® Therapy System can decrease nausea and vomiting symptoms and improve the quality of life for patients with chronic nausea, with or without vomiting, that have normal gastric emptying.

What is the current status of trial NCT06464926?

This trial is currently recruiting. It is a NA study. The enrollment target is 148 participants. The study started on 2025-06-23. Estimated completion is 2030-06.

What conditions does trial NCT06464926 study?

This clinical trial studies the following conditions: Nausea, Vomiting. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06464926?

The interventions under investigation include: Enterra Therapy System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06464926?

This trial is sponsored by Enterra Medical, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06464926 being conducted?

This trial has 17 study locations across Arizona, California, Florida, Illinois, Indiana. 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