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Fluid Resuscitation With HES 200/0.5 10% in Severe Burn Injury

University of Zurich (UZH) logo

University of Zurich (UZH)

Status and phase

Completed
Phase 3

Conditions

Survival
Renal Failure

Treatments

Drug: Fluid resuscitation
Drug: fluid resuscitation

Study type

Interventional

Funder types

Other

Identifiers

NCT01120730
USZ-BURN
97/x (Other Identifier)

Details and patient eligibility

About

HES 200/0.5 10% is equal to ringers lactat solution.

Full description

30 Patients were enrolled to the study, either to the hyperoncotic HES 200/0.5 (10%) group or to the crystalloids only group. After a treatment protocol of 72 hours we collected data about complications like pulmonary failure and abdominal compartment syndrome. Furthermore, we addressed the question of incidence of mortality and renal failure.

Enrollment

28 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • All burn victims with burned surface area bigger than 20%

Exclusion criteria

  • Pregnancy

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

28 participants in 2 patient groups, including a placebo group

HES
Active Comparator group
Description:
Fluid resuscitation with HES
Treatment:
Drug: fluid resuscitation
ringers lactat
Placebo Comparator group
Description:
Standard treatment
Treatment:
Drug: Fluid resuscitation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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