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Glutamate and Diastolic Function in Patients Undergoing Aortic Valve Repair

Glutamate Infusion in Hypertrophied Ventricle After Aortic Valve Replacement - a Randomized Trial

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01144039
Enrollment
27
Registered
2010-06-15
Start date
2006-02-28
Completion date
2008-09-30
Last updated
2010-06-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Aortic Stenosis, Cardiopulmonary Bypass, Hypertrophy, Left Ventricular, Myocardial Ischemia

Brief summary

Purpose: The effect of intravenous glutamate infusion on myocardial diastolic function and overall hemodynamics were studied in patients undergoing elective aortic valve replacement with severe aortic stenosis and associated left ventricular hypertrophy . Methods: 25 patients will be included in this double-blind randomized placebo-controlled study. Glutamate was administered intravenously immediately after aortic cross-clamp release. The patients receive either a low dose of 30mg kg-1 h-1 (LG-group) or high dose of 60 mg kg-1 h-1 (HG-group) or placebo (P-group) at a rate of 3.3ml kg-1h-1 for 2h. Transesophageal echocardiography (TEE) is used to measure diastolic and systolic ventricular function before sternotomy (T0), and 2h (T2), 3h (T3) and 6h (T4) after release of cross clamp. Additionally routine hemodynamic parameters are measured intraoperatively.

Interventions

DRUGLG-group
DRUGHG-group
DRUGPlacebo-group

Sponsors

Medical University of Vienna
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Eligibility

Sex/Gender
ALL
Age
19 Years to 90 Years
Healthy volunteers
No

Inclusion criteria

* severe aortic stenosis * left ventricular hypertrophy of more than 10mm IVS thickness * normal ejection fraction * SR

Exclusion criteria

* moderately or severely reduced systolic left ventricular function (ejection fraction \<30%) * atrial fibrillation or flutter * intolerance to glutamate.

Design outcomes

Primary

MeasureTime frame
E/A ratio
Isovolumic relaxation time
E-velocity
A-velocity
flow propagational velocity

Secondary

MeasureTime frame
cardiac output
mitral ring motion
ejection fraction

Countries

Austria

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026