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Clinical Trials/NCT03443557
NCT03443557CompletedNot Applicable

Effects of Oral Nutrition Supplement in Thai Malnourished Patients : A Cross-sectional Nutrition Day Survey

Pierre Singer1 site in 1 country500 target enrollmentStarted: January 1, 2006Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
500
Locations
1
Primary Endpoint
30-day mortality

Study Overview

Brief Summary

A retrospective study based on Thai data from Nutrition Day study (nD). Comparing clinical outcome between malnourished patients who were prescribed oral nutrition supplement along with hospital diet and those without oral nutrition supplement.

Detailed Description

Prevalence of malnutrition in hospitalized patients varies from 30-70% depend on category of patients recruited. Adverse effects of malnutrition include increase of infection complication, increase hospital length of stay, and increase mortality. Prescription of oral nutrition supplement (ONS) have been proved to provide patients more calorie and protein intake and can improve patients' outcome.

Despite the proved benefits of oral nutrition supplement(ONS), prescription of it in Thai hospitalized patients are far less than it should. The main reason of this under-practice is the limitation of health policies which considered ONS as an optional from main meals. Additional cost for ONS has to be paid by patients themselves, therefore the patients who have no willing to pay usually refuse to receive ONS. Unawareness of physician regarding its benefits is also a problem. In order to convince Thai authorities to allow for reimbursement of ONS and encourage prescription of ONS among physicians, an evidence based benefits of ONS in large Thai population is needed.

The nD study was a single-day, population-based, standardized, multinational, cross-sectional audit and was performed worldwide, includes Thailand, in hospitals, nursing homes and intensive care units performing since 2006 to present. Every year, registered hospitals survey their patients regarding nutritional status, nutritional support. A follow-up for clinical outcome are perform at 30 days after the first survey, include mortality, readmission. This study will based on data of Thai patients collected from nD study during 2006-2016.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Age 18 years old and above
  • •identified as malnourished or at risk

Exclusion Criteria

  • •terminally ill patients
  • •receiving concomitant enteral tube feeding and/or supplemental parenteral nutrition

Outcomes

Primary Outcomes

30-day mortality

Time Frame: 30 days

dead rate at 30 days after study date will be extracted from hospital medical record by hospital staff

Secondary Outcomes

  • Discharge rate(30 days)
  • Hospital length of stay(30 days)
  • Re-admission rate(30 days)

Investigators

Sponsor
Pierre Singer
Sponsor Class
Other
Responsible Party
Sponsor Investigator
Principal Investigator

Pierre Singer

Professor

Rabin Medical Center

Study Sites (1)

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