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A Trial of Intravenous Calcium and Myocardial Diastolic Dysfunction During Separation From Cardiopulmonary Bypass

Phase 4
Terminated
Conditions
Diastolic Dysfunction
Interventions
Registration Number
NCT00955266
Lead Sponsor
Brigham and Women's Hospital
Brief Summary

Successful heart surgery requires the resumption of a strong beating heart prior to separation from the heart and lung machine. There are different ways to do this. At this hospital, the surgical team usually gives calcium to people when they come off of the heart and lung machine because some doctors believe that calcium can "jump start" the heart. Not every hospital does this.

Some people think that calcium may have a side effect of making the heart more stiff. Stiff hearts do not beat as well or receive as much blood to tissues as non-stiff hearts. If calcium makes the heart stiff, then doctors may have to use other medicines to support the heart in the operating room and the intensive care unit. This may ultimately lead to poorer outcomes including a longer stay in the intensive care unit and in the hospital.

This study is being performed to find out if calcium has the side effect of making the heart more stiff. This study compares calcium to placebo. The placebo looks exactly like the calcium, but it contains no calcium. During this study patients may receive placebo instead of calcium. Neither the doctor nor the study team will know which drug the subject will receive.

Detailed Description

Not available

Recruitment & Eligibility

Status
TERMINATED
Sex
All
Target Recruitment
8
Inclusion Criteria
  • Men and women greater than 18 years of age
  • Undergoing primary elective valve surgery at Brigham and Women's Hospital
  • Consented for Transesophogeal Echocardiography (TEE) as part of routine intra-operative care and monitoring
Exclusion Criteria
  • Patients not consented for TEE as part of routine intra-operative care
  • Any absolute contraindication to TEE
  • Ionized calcium level < 0.80 mmol/L near separation from CPB
  • Myocardial infarction (MI) or acute coronary syndromes < 3 months prior to surgery due to the presence of pre-operative diastolic dysfunction in infarcted or ischemic myocardium
  • Ejection fraction (EF) < 35%
  • Atrial fibrillation / flutter the absence of an A wave on mitral inflow Doppler
  • Heart rate (HR) > 100 during 2 data point collections due to E / A wave superimposition

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboNormal saline
Calcium ChlorideCalcium ChlorideCalcium chloride, 10mg/kg
Primary Outcome Measures
NameTimeMethod
Diastolic Dysfunction64 enrolled patients or 9 months following start of protocol, whichever comes first

E/ A ratio on TEE. This ratio of peak velocity flow in early diastole (the E wave) to peak velocity flow in late diastole caused by atrial contraction (the A wave) is reflective of degree of diastolic dysfunction.

Secondary Outcome Measures
NameTimeMethod
Return to Cardiopulmonary Bypass Secondary to Hemodynamic Instability64 enrolled patients or 9 months following start of protocol, whichever comes first

Return to Cardiopulmonary bypass Yes/ No

Need for Inotropic or Vasopressor Support Upon Leaving the OR64 enrolled patients or 9 months following start of protocol, whichever comes first

Use of inotropes or vasopressors in the Operating Room.

Length of ICU Stay (Days)64 enrolled patients or 9 months following start of protocol, whichever comes first

Intensive Care Unit length of stay in days.

Length of Hospital Stay (Days)64 enrolled patients or 9 months following start of protocol, whichever comes first

Hospital length of stay in days.

Trial Locations

Locations (1)

Brigham and Womens Hospital

🇺🇸

Boston, Massachusetts, United States

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