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Safety and Effectiveness of A Novel Enteral Feeding System: Prospective Study.

NCT06173063 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 19

Last updated 2025-12-29

Study results available
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Summary

The goal of this interventional study is to obtain information on the safety and effectiveness of a novel enteral feeding system in adult users requiring at least a portion of their nutritional intake via enteral feeding. The main questions it aims to answer are:

* Can the device be used safely and effectively?
* Does use of the device impact on patient's quality of life?

Participants will use Mobility+ enteral feeding system as their enteral feeding method for the duration of the study and will record their experiences.

Conditions

  • Enteral Feeding

Interventions

DEVICE

Mobility+ Enteral Feeding System

Enteral feeding using a continuous feeding, self-powered, discreet, silent enteral feeding system.

Sponsors & Collaborators

  • Horizon 2020 - European Commission

    collaborator OTHER

  • Rockfield Medical Devices

    lead INDUSTRY

Principal Investigators

  • Manpreet Mundi · Mayo Clinic

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2023-11-14
Primary Completion
2024-11-06
Completion
2024-11-06
FDA Device
Yes

Countries

  • United States

Study Locations

More Related Trials

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 NCT06173063 on ClinicalTrials.gov