Clinical Trials Directory

Trials / Unknown

UnknownNCT04507672

Acetated Ringer's Solution Versus Saline in Patients With Septic Shock

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
2,000 (estimated)
Sponsor
Southeast University, China · Academic / Other
Sex
All
Age
18 Years – 90 Years
Healthy volunteers
Not accepted

Summary

The primary aim of this trial is to compare the effect of acetated ringer's solution with that of saline for therapy on the incidence and development of major adverse renal events among septic shock patients. The investigators hypothesize that use of acetated ringer's solution for resuscitation among septic shock patients will reduce the incidence of major adverse kidney events.

Detailed description

Normal saline and Ringer's solutions are the preferred crystalloid fluids administered in early septic shock. However, evidence have associated saline with hyperchloremia and secondary metabolic acidosis, and renal vasoconstriction, increased incidence of acute kidney injury (AKI) and mortality. The primary aim of this trial is to compare the effect of acetated ringer's solution with that of saline for therapy on the incidence and development of major adverse renal events among septic shock patients. The investigators hypothesize that use of acetated ringer's solution for resuscitation among septic shock patients will reduce the incidence of major adverse kidney events.

Conditions

Interventions

TypeNameDescription
DRUGFluid resuscitationUse the choice of crystalloid for resuscitation during the first 72 hours after enrollment

Timeline

Start date
2020-09-01
Primary completion
2023-10-01
Completion
2023-12-01
First posted
2020-08-11
Last updated
2020-08-11

Source: ClinicalTrials.gov record NCT04507672. Inclusion in this directory is not an endorsement.