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Oral Nutritional Supplement in Adults With or at Risk of Malnutrition

NCT07426406 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2026-07-01

No results posted yet for this study

Summary

This is a multi-center, prospective, non-randomized, non-blinded, single-arm, single treatment study.

Conditions

  • Gastrointestinal Tolerance

Interventions

OTHER

Experimental Nutrition Product

High energy, high protein oral nutritional supplement

Sponsors & Collaborators

  • Abbott Nutrition

    lead INDUSTRY

Principal Investigators

  • Maria Camprubi, PhD · Abbott

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-03-22
Primary Completion
2026-06-30
Completion
2026-06-30

Countries

  • United Kingdom

Study Locations

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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 NCT07426406 on ClinicalTrials.gov