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Serial Body Composition Change for Risk Prediction and Nutritional Guide in Treating Patients With Sepsis

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Chang Gung Medical Foundation

Status

Completed

Conditions

Sepsis

Treatments

Dietary Supplement: Nutritional intervention

Study type

Interventional

Funder types

Other

Identifiers

NCT04989569
201901875A3C501

Details and patient eligibility

About

To explore whether serial changes of data in body composition of patients with sepsis can help clinician to monitor prognosis.

Full description

The investigators will use the random number generator to divide the patients into two groups, the control group (with no nutritional intervention) and the intervention group (with nutritional intervention). The body composition data (of day 1, 3, 8) of the patients in the intervention group will be given to the dietitians for adjusting the diet formula according to the patient's body composition.The patients in control group also will undergo Bio-electrical Impedance Analysis (BIA) assessment, but not disclosed to the dietitian. The diet formula will be adjusted on the discretion of the dietitian caring for the septic patients based on clinical judgement.

Enrollment

132 patients

Sex

All

Ages

18 to 100 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. ICU patient
  2. Clinical diagnosis of sepsis

Exclusion criteria

  1. Expired within 3-days

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

132 participants in 2 patient groups

control
No Intervention group
Description:
The investigators will use the random number generator to divide the patients into two groups, the control group (with no nutritional intervention) and the intervention group (with nutritional intervention). The body composition data (of day 1, 3, 8) of the patients in the control group will not be given to the dietitians for adjusting the diet formula according to the patient's body composition.
nutritional intervention
Experimental group
Description:
The investigators will use the random number generator to divide the patients into two groups, the control group (with no nutritional intervention) and the intervention group (with nutritional intervention). The body composition data (of day 1, 3, 8) of the patients in the intervention group will be given to the dietitians for adjusting the diet formula according to the patient's body composition.
Treatment:
Dietary Supplement: Nutritional intervention

Trial contacts and locations

1

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Central trial contact

FANG WEN-FENG; HUNG KAI-YIN

Data sourced from clinicaltrials.gov

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