Milrinone Inhaled in Cardiac Surgery
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Purpose
Pulmonary hypertension is an important morbidity factor in patients having to undergo cardiac surgery with cardiopulmonary bypass (ECC). Milrinone used in inhalation, shows evidence of being a pulmonary vasodilator able to possibly contribute to the reduction of pressure on the pulmonary artery.
| Condition | Intervention | Phase |
|---|---|---|
|
Valvular Stenosis Valvular Insufficiency Hypertension, Pulmonary Coronary Artery Disease |
Drug: Milrinone Drug: Normal saline |
Phase 2 |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Safety/Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Investigator) Primary Purpose: Treatment |
| Official Title: | 2- Inhaled Milrinone Prevents the Increase in Pulmonary Artery Pressure After CPB |
- To demonstrate that inhaled milrinone administered before CPB is superior to placebo in reducing the severity of difficult separation from bypass [ Time Frame: End of CPB ] [ Designated as safety issue: Yes ]
- Reduction in morbidity and mortality post-op [ Time Frame: At discharge, 3 months, 6 months and 1 year by telephone ] [ Designated as safety issue: Yes ]
- Reduction in pulmonary artery pressure [ Time Frame: Same day before and after CPB ] [ Designated as safety issue: Yes ]
- Right ventricular function measured using transthoracic echocardiography (TTE) and TEE [ Time Frame: Same day before and after the CPB ] [ Designated as safety issue: Yes ]
- Serum levels of milrinone in relation with the pharmacodynamic marker [ Time Frame: Same day pre CPB per CPB and post CPB ] [ Designated as safety issue: Yes ]
- reduction of the composite index of hemodynamic complications (defined as hospital death, vasoactive drugs > 24 hours and post-op cardiac arrest), [ Time Frame: 24 hrs post op and hospital discharge ] [ Designated as safety issue: Yes ]
| Estimated Enrollment: | 124 |
| Study Start Date: | February 2009 |
| Estimated Study Completion Date: | December 2012 |
| Primary Completion Date: | January 2012 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Placebo Comparator: Normal saline
Normal saline by inhalation over 15 min
|
Drug: Normal saline
5 ml normal saline by inhalation over 15 min
Other Names:
|
|
Active Comparator: Milrinone
Inhaled milrinone 5 mg(as for the injectable solution)
|
Drug: Milrinone
inhaled milrinone 5 mg (as for the injectable solution)
Other Names:
|
Detailed Description:
This controlled, randomized, double-blind study will aim at confirming the efficiency as well as the security of Milrinone, used in inhalation, to diminish the degree of pulmonary hypertension before the cardiopulmonary bypass (ECC) circulation. In addition, the pharmacokinetic and echo graphic repercussions of administering the medication will be analysed. At the present time, there is no data on the pharmacokinetics of the medication when it's administered through inhalation. For this reason, we would like to study the serous rate of the medication in the minutes following its administration through inhalation.
Eligibility| Ages Eligible for Study: | 18 Years to 90 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
- Adult patients scheduled for elective valvular or complex (2 or more valves or
- valve and revascularization) cardiac surgery under CPB with preoperative PHT defined as mean pulmonary artery pressure (MPAP) over 30 mmHg or
- systolic pulmonary artery pressure (SPAP) over 40 mmHg (using preoperative right-sided catheterization or estimated by echocardiography).
Exclusion Criteria:
- Cardiac surgery not requiring CPB, contraindication to TEE (esophageal pathology or unstable cervical spine) and emergency surgery.
- Patients will be recruited the day before surgery and randomized using computerized cards by the pharmacy department
Contacts and Locations| Canada, Quebec | |
| Montreal Heart Institute | |
| Montreal, Quebec, Canada, H1T 1C8 | |
| Principal Investigator: | Denault André, MD FRCPC | Montreal Heart Institute |
More Information
Publications:
| Responsible Party: | Andre Denault, MD FRCPC ABIM-CCM, Montreal Heart Institute |
| ClinicalTrials.gov Identifier: | NCT00819377 History of Changes |
| Other Study ID Numbers: | 08-1004 |
| Study First Received: | January 8, 2009 |
| Last Updated: | April 25, 2012 |
| Health Authority: | Canada: Ethics Review Committee |
Keywords provided by Montreal Heart Institute:
|
Valvular surgery pulmonary artery pressure |
Additional relevant MeSH terms:
|
Coronary Artery Disease Myocardial Ischemia Coronary Disease Hypertension Hypertension, Pulmonary Heart Diseases Cardiovascular Diseases Arteriosclerosis Arterial Occlusive Diseases Vascular Diseases Lung Diseases Respiratory Tract Diseases Milrinone |
Platelet Aggregation Inhibitors Hematologic Agents Therapeutic Uses Pharmacologic Actions Vasodilator Agents Cardiovascular Agents Phosphodiesterase 3 Inhibitors Phosphodiesterase Inhibitors Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action Cardiotonic Agents Protective Agents Physiological Effects of Drugs |
ClinicalTrials.gov processed this record on May 23, 2013