Coronary Heart Disease Clinical Trial
Official title:
A Phase , Prospective, Randomized, Open-label Study to Compare the Efficacy and Safety of Hypertonic Sodium Lactate Solution Compared With 6% HES Solution in CABG (Coronary Artery Bypass Grafting) Patients
The choice of fluid therapy is controversial in cardiac surgery. Numerous studies have shown that colloid is better as compared to crystalloids. Several previous studies have demonstrated that Hypertonic Sodium Lactate (HSL) administration during cardiac surgery shows a promising effect. This study aims to compare hemodynamic effects and fluid balance of HSL with 6% Hydroxy Ethyl Starch (HES).
The primary objectives of this prospective, randomized and open-label study are as follows:
- To evaluate the clinical efficacy of Hypertonic Sodium Lactate (HSL) in comparison with
6% HES to maintain hemodynamic stability in intra CABG patients related to hemodynamic
status and Body fluid balance.
- To assess the safety of HSL in intra CABG patients related to defined laboratory
parameters clinical adverse events which occur during the trial.
Subjects meeting enrolment criteria will be randomly assigned to HSL or 6%HES treatment
groups.
Assessment of comparability will be done by unpaired student t-test or Chi-Square test or by
a two-way ANOVA for repeated measures followed by post-hoc analysis when significant
difference is found within the two groups.
The hypothesis tested is that HSL is effective in intra CABG surgery patients, requiring
less volume with better cardiac index, as compared to 6% HES.
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment
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