Lactated Ringer's and PlasmaLyte in Critically Ill Adults

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

12000 participants

Study Classification

OBSERVATIONAL

Study Start Date

2018-01-13

Study Completion Date

2019-02-28

Brief Summary

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In recent years, there has been a large amount of literature reports that normal saline can increase the incidence of renal injury in critically ill patients compared with balanced salt solution.However, no studies have compared the effects of different types of balanced salt solutions on the incidence of renal injury.

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Detailed Description

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Conditions

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Critical Illness

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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Mix group

Patients who used two balanced salt solutions during icu stay

RL

Intervention Type DRUG

lactated Ringer's

PLA

Intervention Type DRUG

PlasmaLyte

RL group

Patients who have only used lactated Ringer's during icu stay

RL

Intervention Type DRUG

lactated Ringer's

PLA group

Patients who have only used PlasmaLyte during icu stay

PLA

Intervention Type DRUG

PlasmaLyte

Interventions

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RL

lactated Ringer's

Intervention Type DRUG

PLA

PlasmaLyte

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* All patients admitted to ICU

Exclusion Criteria

* Patients \<18 year old when admission
* Patients who stay less than 24 hours in ICU
* Patients who do not sufficient data for further analysis
* Readmission patients during the study period

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No