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CompletedNCT03379116Updated Dec 21, 2017

A Study on Nutrition Support in Adult Patients With Severe Burns

An observational study in Severe Burn and Enternal Nutrition, sponsored by Southeast University, China. Completed. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2017-12-21.

Sponsored by Southeast University, China · Observational

Study type
Observational
Model
Case-only
Time perspective
Retrospective
Enrollment
100
Ages
18 Years and older
Sex
All
01

Study summary

To delineate nutritional support in adults patients with severe burns to investigate associations between nutritional practice and clinical outcomes.

02

Conditions studied

  • Severe Burn
  • Enternal Nutrition

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03

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

The study was a prospective, observational, multicenter trial and was conducted in intensive care units of seven hospitals participating in the treatment of the burn patients. Patients who were at least 18 years of age were eligible if they were expected to survive more than 48 hours.

Inclusion criteria

  • Patients were at least 18 years of age
  • Patients were expected to survive more than 48 hours.

Exclusion criteria

Exclusion Criteria:

  • irreversible disease
04

Study design

Observational model
Case-only
Time perspective
Retrospective
Enrollment
100 participants (actual)
Patient registry
No

Interventions

  • Otherenteral nutrition and parenteral nutrition

    In the treatment of the burned patients injured,data on nutritional support and patient's outcomes were collected and analyzed.

05

What researchers measure

Primary outcomes

  1. Mortality at 28 days

    Daily data were recorded for a maximum of 28 days per patient. Patients alive in hospital at the 28th day or discharged prior to 28 days were considered to be survivors.

    Time frame: 28days

06

Study locations

No study locations are listed for this record.

07

Registry details

Key details

Study ID
NCT03379116
Lead sponsor
Southeast University, China
Responsible party
Ling Liu (chief, Southeast University, China) — Principal investigator
First posted
Dec 20, 2017
Start date
Jun 2, 2014
Primary completion
Sep 24, 2014
Completion
Oct 2, 2014
Last update
Dec 21, 2017

Oversight

FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Dec 2017. You cannot join it, but the record below documents what was studied.

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