NCT06173063

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

• Status: Terminated
• Phase: N/A
• Study type: Interventional
• Enrollment: 19 (actual)
• Sponsor: Rockfield Medical Devices · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

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.

Detailed description

The study will allow 25 participants to use the Mobility+ system for their feeding sessions over the course of 14 consecutive days, following an initial 7-day period where participants have time to trial and get used to the new system. Participants' homes are the setting for the 21-day study duration.

Conditions

• Enteral Feeding

Interventions

Type	Name	Description
DEVICE	Mobility+ Enteral Feeding System	Enteral feeding using a continuous feeding, self-powered, discreet, silent enteral feeding system.

Timeline

• Start date: 2023-11-14
• Primary completion: 2024-11-06
• Completion: 2024-11-06
• First posted: 2023-12-15
• Last updated: 2025-12-29
• Results posted: 2025-12-29

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study