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Liquid Nutritional Supplement on Malnutrition Hospitalized Patient

U

University of Indonesia (UI)

Status

Unknown

Conditions

Malnutrition

Treatments

Dietary Supplement: Liquid Nutritional Supplement from Hospital Product
Dietary Supplement: Placebo

Study type

Interventional

Funder types

Other

Identifiers

NCT04036825
19-01-0082

Details and patient eligibility

About

The aim of this study is to know the effectivity of liquid nutritional supplementation in malnutrition hospitalized patients

Enrollment

138 estimated patients

Sex

All

Ages

18 to 60 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • aged ≥ 18 years old to 60 years old
  • malnutrition hospitalized patient based on European Society for Clinical Nutrition and Metabolism (ESPEN) 2015 criteria
  • agreed to participate

Exclusion criteria

  • malignancy
  • chronic kidney disease stage III-V
  • decompensated hepatic cirrhosis
  • allergic to milk or lactose intolerance
  • could not be randomised and participate in this study by clinical judgement

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

138 participants in 2 patient groups, including a placebo group

Liquid Nutritional Supplement from Hospital Product
Experimental group
Description:
This group received liquid nutritional supplement from hospital product. The product is in a form of low lactose milk ready to drink with volume 200 ml and will be given 2 times daily for 14 days. This product is consist of 1.017 kcal/ml, 10 vitamin and 9 mineral
Treatment:
Dietary Supplement: Liquid Nutritional Supplement from Hospital Product
Placebo
Placebo Comparator group
Description:
This group received standard liquid nutritional supplement as a placebo. Placebo will be given 2 times daily for 14 days
Treatment:
Dietary Supplement: Placebo

Trial documents
1

Trial contacts and locations

1

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Central trial contact

Marcellus Simadibrata

Data sourced from clinicaltrials.gov

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