Pilot Study of the Entarik System With Advanced Functionality in Health Adults

Last updated: July 8, 2025
Sponsor: Gravitas Medical, Inc.
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

Feeding tube (Entarik)

Clinical Study ID

NCT06660758
CRD-04-1934-01
  • Ages > 18
  • All Genders
  • Accepts Healthy Volunteers

Study Summary

In this single-site study, data will be recorded during nasogastric or orogastric placement (and post-pyloric placement) and removal of the Entarik Feeding Tube. Data will also be collected prior to, during, and following the delivery of a meal through the feeding tube.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. At least 18 years old

  2. Able to provide informed consent

  3. Capable and willing to follow all study-related procedures

  4. Confirmed fasted state for a minimum of 8 hours prior to study initiation

Exclusion

Exclusion Criteria:

  1. Inability to receive a feeding tube

  2. Known self-reported history of hiatal hernia, esophagitis, esophageal strictures orgastric ulcers

  3. Has a basilar skull fracture

  4. Self-reports pregnancy

  5. Deemed unsuitable for enrollment in study by the investigator based on subjects'history or physical examination

Study Design

Total Participants: 40
Treatment Group(s): 1
Primary Treatment: Feeding tube (Entarik)
Phase:
Study Start date:
October 22, 2024
Estimated Completion Date:
December 22, 2025

Connect with a study center

  • Gravitas Medical, Inc.

    Berkeley, California 94710
    United States

    Active - Recruiting

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