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A Comparison of Efficacy and Safety of Complete Nutrition Formula and Standard Complete Medical Tube Feeding For-mula in Nasogastric Tube Fed Patient

A Comparison of Efficacy and Safety of Complete Nutrition Formula and Standard Complete Medical Tube Feeding Formula in Nasogastric Tube Fed Patient

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
TCTR
Registry ID
TCTR20250731005
Enrollment
15
Registered
2025-07-31
Start date
2025-05-02
Completion date
Unknown
Last updated
2026-08-03

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

Conditions

A subjects required nasogastric tube feeding for at least 14 days before inclusion of this study. NG tube, Nutrition, Meal replacement

Interventions

The subjects received complete nutrition formula at the dose of 30 kcal/kg. BW/day for 7 days.
Experimental Dietary Supplement
Complete nutrition formula

Sponsors

UDEENA GLOBAL CO., LTD., Thailand
Lead Sponsor

Eligibility

Sex/Gender
All
Age
40 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Aged between 40 and 99 years 2. Subjects are considered suitable for transition to nasogastric tube feeding with a standard formula. 3. Cardiovascular stability was required, demonstrated by a resting heart rate of less than 120 beats per minute and a mean arterial pressure (MAP) greater than or equal to 65 mmHg.

Exclusion criteria

Exclusion criteria: 1. Subjects being diagnosed with severe malnutrition, acute illnesses, gastrointestinal ob-struction or gastro-intestinal dysmotility, diarrhea (at least three episodes of loose stools per day), significant liver and gallbladder issues in their medical history. 2. Subjects were require specific nutritional management for disease-related symptoms. 3. Subjects allergies to soy, dairy proteins, rice bran oil, medium-chain triglyceride (MCT) oil, or sodium caseinate. 4. . Subjects received corticosteroids at a dosage greater than 2 mg/kg of body weight within the two weeks before enrollment. 5. Women who were pregnant or breastfeeding were also not eligible for this study.

Design outcomes

Primary

MeasureTime frame
Weight 7 day after intervention Weight measurement

Secondary

MeasureTime frame
BMI 7 day after intervention Calculated from weight and height

Countries

Thailand

Contacts

Public ContactJiraporn Laoungon

Chiang Mai University

jiraporn.l@cmu.ac.th053942508

Outcome results

None listed

Source: TCTR (via WHO ICTRP) · Data processed: Aug 10, 2026