Clinical Trials Directory

Trials / Completed

CompletedNCT05914896

Hyperosmolality and Acute Kidney Injury After Cardiac Surgery

Hyperosmolar Priming Solution for Cardiopulmonary Bypass May Increase the Risk for Postoperative Acute Kidney Injury: Results From Double-blinded Randomised Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
200 (actual)
Sponsor
Umeå University · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Not accepted

Summary

The goal of this randomized controlled trial is to test if a hyperosmolar prime solution used for cardiopulmonary bypass increases the risk for acute postoperative kidney injury.

Detailed description

Two-hundred cardiac surgical patients were randomised into two groups based on the osmolality level of the prime solution used for cardiopulmonary bypass. The high osmolality group (966 mOsm) received a prime solution containing Ringer-Acetate 1000 ml + Mannitol 400 ml (60 g) + Sodium-Chloride 40 ml (160 mmol) and Heparin 2 ml (10 000 IU), while the reference group with normal osmolality (388 mOsm) received a prime solution containing Ringer-Acetate 1400 ml and Heparin 2 ml (10 000 IU).

Conditions

Interventions

TypeNameDescription
DRUGHighOsmoThis group received a priming solution with high osmolality

Timeline

Start date
2019-04-24
Primary completion
2020-06-24
Completion
2020-06-24
First posted
2023-06-22
Last updated
2023-06-22

Locations

1 site across 1 country: Sweden

Source: ClinicalTrials.gov record NCT05914896. Inclusion in this directory is not an endorsement.