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

Status: Recruiting
Location: See all (2) locations...
Intervention Type: Dietary supplement
Study Type: Interventional
Study Phase: Not Applicable
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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1
Healthy Volunteers: f
View:

• Patients from 1 -15 years for children and 15 years and above for adults of requiring 1 or more bolus tube feed alongside their usual tube feed or home-made blended diet as part of their dietary management for disease related malnutrition.

• Patients well-established and stable on current enteral tube feed or home-made blended diet.

• Gastrostomy fed only.

• Willingly given, written, informed consent from patient/caregiver

Locations
Other Locations
United Kingdom
Queen Medical Hospital Nutrition and Dietetics
NOT_YET_RECRUITING
Nottingham
Dietetic Team 1st floor Kings Court 1, Charles Hastings Way,
RECRUITING
Worcester
Contact Information
Primary
Sharan Saduera, BSc (Hons) Dietetics
sharan.saduera@uk.nestle.com
+447557170649
Backup
Sarah Durnan, PHD, BSc Nutrition Dietetics
Time Frame
Start Date: 2025-12-10
Estimated Completion Date: 2026-11-11
Participants
Target number of participants: 50
Treatments
Other: Acceptability and Tolerance Study of bolus tube feed with food blends
Arm one will act as their own controls
Sponsors
Leads: Société des Produits Nestlé (SPN)

This content was sourced from clinicaltrials.gov