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Colloid Improves Organs Function in Resuscitation of Extensive Burn Patients

NCT01939613 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 47

Last updated 2013-09-11

No results posted yet for this study

Summary

The present study was to evaluate the effectiveness of colloid compared with crystalloids for fluid resuscitation in critical burn patients with total burn surface area ≥50%.

Conditions

  • Burn

Interventions

DRUG

colloids

TMMU group allows for administration of colloids early,while Parkland group infuse colloids 24 h after burn injury.

Sponsors & Collaborators

  • Tang-Du Hospital

    lead OTHER

Principal Investigators

  • Xueyong Li, MD · Department of Burn and Plastic Sugery

Eligibility

Min Age
19 Years
Max Age
60 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-07-31
Primary Completion
2013-06-30
Completion
2013-07-31

Countries

  • China

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01939613 on ClinicalTrials.gov