drugset / Trial / NCT00529711

The Efficacy of Hypertonic Lactate Solution in CABG(Coronary Artery Bypass Grafting) Patients

NCT00529711

Phase 3 Completed 66 enrolled Innogene Kalbiotech Pte. Ltd
RandomizedParallel-groupOpen-labelTreatment

Summary

Previous clinical trials with 11.2% Hypertonic Ringer's Lactate in post-operative CABG subjects have shown an increase in several cardiac performance parameters, with lesser volume of resuscitation fluid required to reach circulation volume, as compared to Sodium Chloride.It also does not cause hyperchloremic acidosis, which is of value in treating shock patients. The primary objectives of this prospective, randomized, open-label trial are to evaluate the clinical efficacy of hypertonic lactate in comparison to Ringer's lactate to maintain hemodynamic stability in intra- and post-CABG subjects in relation to hemodynamic status and body fluid balance, as well as to assess its safety in terms of lab parameters and occurrence of adverse events.The secondary objectives are to evaluate comparative clinical efficacy of the two fluids in relation to reduction in concomitant drug utilization, duration of ventilator usage, length of stay in ICU as well as total duration of hospitalization and neurocognitive status upto a period of 1 year post-CABG.

Timeline

Start
2005-07
Primary completion
Completion
2006-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Hypertonic lactate Unknown Other
Comparator Ringer's Lactate Other / unclassified Other

Indications