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Nutritional supplementation and length of stay: a controlled trial of nutritional supplementation in a mixed acute hospital setting

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN78277754
Enrollment
Unknown
Registered
2004-01-23
Start date
1997-09-01
Completion date
Unknown
Last updated
2015-01-13

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Other symptoms and general pathology Signs and Symptoms Symptoms and signs concerning food and fluid intake

Interventions

1. Palatable liquid oral sip feed with vitamin supplements 2. Placebo (palatable liquid oral sip feed only)

Sponsors

NHS R&D Regional Programme Register - Department of Health (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Patients admitted acutely to general medicine, general surgery and orthopaedics. 2. Patients with a body mass index <22 within the above sample, will be randomized to oral sipfeed or placebo feed, independent of whether they are receiving vitamin supplements.

Exclusion criteria

Exclusion criteria: 1. Planned admission to medical or orthopaedic wards or to wards other than those 15 taking part in the study. 2. Less than 18 years 3. Mental illness 4. Admission for only 2 days

Design outcomes

Primary

MeasureTime frame
1. It is expected that a significant incidence of biochemical water soluble vitamin deficiency will be detected among the patients admitted via accident and emergency and that HPLC of single blood samples, will provide a reliable method for assay, and prove much more rapid and convenient than the established enzymatic methods of routine screening. 2. The incident of protein/energy malnutrition detected by anthropometric assessment is expected to approximate 40% in the study group of patients. 3. Previous studies suggest that we might expect a reduction of length of stay as a result of feed supplementation of undernourished inpatients. We might also see reductions in mortality in this group. 4. We might detect a reduction in length of stay and mortality as a result of water soluble vitamin supplementation, either in the study population as a whole, or within subgroups identified in the course of the study.

Secondary

MeasureTime frame
Not provided at time of registration

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026