A Study on Nutrition Support in Adult Patients With Severe Burns

December 20, 2017 updated by: Ling Liu, Southeast University, China
To delineate nutritional support in adults patients with severe burns to investigate associations between nutritional practice and clinical outcomes.

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Actual)

100

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years and older (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

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.

Description

Inclusion Criteria:

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

Exclusion Criteria:

  • irreversible disease

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Mortality at 28 days
Time Frame: 28days
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.
28days

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Southeast University, China

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

June 2, 2014

Primary Completion (Actual)

September 24, 2014

Study Completion (Actual)

October 2, 2014

Study Registration Dates

First Submitted

December 15, 2017

First Submitted That Met QC Criteria

December 15, 2017

First Posted (Actual)

December 20, 2017

Study Record Updates

Last Update Posted (Actual)

December 21, 2017

Last Update Submitted That Met QC Criteria

December 20, 2017

Last Verified

December 1, 2017

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • 20171215

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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