Oral Nutritional Supplementation in Hospital Patients

Launched by ABBOTT NUTRITION · Jul 16, 2012

Keywords

ClinConnect Summary

Approximately 212 subjects (men and women) from multiple Institutions in India will participate in this study. Eligible subjects will be randomized into 2 treatment groups.

* Dietary Counseling only (n=106)
* Dietary Counseling + ONS (n=106)

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • ≥ 18 years of age
• • Recently admitted into hospital ≤36 hrs.
• • Identified as having "moderate malnutrition" or "severe malnutrition".
• • Anticipated length of hospital stay of at least 3 days.
• • Life expectancy of ≥ 12 weeks
• • Able to consume foods and beverages orally.
• • Willing to abstain from nutritional supplements throughout the study period unless provided be study.
• Exclusion Criteria:
• • Alcohol or substance abuse, severe dementia, brain metastases, eating disorders or any psychological condition that may interfere with dietary intake, severe nausea, dysphagia, vomiting, diarrhea, active gastritis, gastrointestinal bleeding or other gastrointestinal disturbances.
• • Diabetes, burn injury covering greater than or equal to 15% of the body, advanced renal or hepatic disease, active malignancy.
• • Ascites, pleural effusion, severe edema or dehydration.
• • Severe edema.
• • Medications/ supplements/substances that could profoundly modulate metabolism or weight
• • Active tuberculosis, acute Hepatitis B or C, or HIV.