NCT07341464

Acceptability and Tolerance Study of Bolus Tube Feed With Food Blends

Acceptability (Including Gastrointestinal Tolerance and Compliance) of a Paediatric and Adult Bolus Tube Feed With Food Blends

• Status: Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 50 (estimated)
• Sponsor: Société des Produits Nestlé (SPN) · Industry
• Sex: All
• Age: 1 Year
• Healthy volunteers: Not accepted

Summary

This is a prospective acceptability study to evaluate the gastrointestinal tolerance and compliance of a bolus tube feed over a 28 -day period for up to 50 participants. The enteral bolus formula is for the dietary management of patients with short bowel syndrome; intractable malabsorption; preoperative preparation of undernourished patients; inflammatory bowel disease; total gastrectomy; dysphagia; bowel fistulae; feeding intolerances, developmental disabilities, and disease related malnutrition.

Detailed description

The study will collect data in 50 children and adults over a period of 28 days. Gastrointestinal tolerance will be collected over 7 days and formula intake will be over 28 days. A patient satisfaction questionnaire will be completed at the end of the study.

Conditions

• Cerebral Palsy (CP)
• Oncology

Interventions

Type	Name	Description
DIETARY_SUPPLEMENT	Tube feed	Dose intake and duration.

Timeline

• Start date: 2025-12-10
• Primary completion: 2026-11-10
• Completion: 2026-11-11
• First posted: 2026-01-14
• Last updated: 2026-01-14

Locations

2 sites across 1 country: United Kingdom