Effect of Early Enteral Tube Feeding Nutrition With an Immune Enhancing Diet in Severe Burn Patients

Status

Completed

Phases

Phase 4

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT00561210

Enrollment

Registered

2007-11-20

Start date

2003-11-30

Completion date

2010-03-31

Last updated

2013-11-19

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

Conditions

Infections on, Severe Burn Patients

Keywords

infections

Brief summary

Compare clinical and biological effects of two enteral tube feeding nutrition formula (immune enhancing diet versus polymeric diet)in severe burn hospitalized patients .

Interventions

DIETARY_SUPPLEMENTCrucial

Treatment between minimum 14 days and maximum 6 months. Apports depend on method of CURRERI.

DIETARY_SUPPLEMENTSondalis HP

Treatment between minimum 14 days and maximum 6 months. Apports depend on method of CURRERI.

Study design

Allocation

RANDOMIZED

Intervention model

PARALLEL

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

15 Years to 70 Years

Healthy volunteers

Inclusion criteria

* Thermic burn from 20% to 80% * 15 \< age \< 70 years * written informed consent

Exclusion criteria

* diabetes mellitus * corticoid or immuno-suppressive therapy * HIV * evolutive cancers * pregnancy * abdominal lesion * hepatic or renal failure

Design outcomes

Primary

Measure	Time frame
Number of infections and number of multiple organ failure	6 months

Secondary

Measure	Time frame
digestive tolerance and healing	6 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026