Supernormal Oxygen Delivery for Patients With Severe Burns

Early Phase 1UnknownNCT05241912

Guangzhou Red Cross Hospital100 enrolled

Overview

This is a randomized double-blinded study to investigate in which the groups are designated as the control group and the goal-directed fluid therapy group to further evaluate significant differences in rate of complications during burn surgery.

This is a randomized double-blinded study to investigate the effect of control group and the goal-directed fluid therapy group on complications during surgery of the burn patients. The groups are designated as the control group and the oal-directed fluid therapy group to further evaluate significant differences in complications during the surgery.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

PREVENTION

Masking

QUADRUPLE

Enrollment

100

Conditions

Burn Surgery Dobutamine

Interventions

DobutamineDRUG

administration of dobutamine 0.01 - 0.04 U/min after induction of anesthesia to maintain oxygen delivery

Eligibility

Sex: ALLMin age: 18 YearsMax age: 60 Years

Medical Language ↔ Plain English

Inclusion Criteria: * Severe burn patients Exclusion Criteria: * Patients or families refuse to sign consent

Locations (1)

Guangzhou Red cross hospital

Guangzhou, Guangdong, China

Outcomes

Primary Outcomes

Complication

perioperative complications

Time frame: One week after operation

Data from ClinicalTrials.gov

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