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Iloprost-Study: Comparison of Nitric Oxide to Iloprost (Ventavis) for Treatment of Pulmonary Hypertension in Children After Cardiopulmonary Bypass Surgery

Primary Purpose

Pulmonary Hypertension

Status
Completed
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
aerosolized iloprost
Sponsored by
Heidelberg University
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Pulmonary Hypertension focused on measuring Pulmonary hypertension, Cardiac Surgery, Children, Pediatric Patients, Iloprost, NO, nitric oxide, Pulmonary hypertension after cardiac surgery in pediatric patients, 0 - 2 years old

Eligibility Criteria

undefined - 2 Years (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Informed consent by parents or legal representatives Age: Infants older than 4 weeks of age and children less than 1½ years of age. Presence of a left-to-right shunt with increased pulmonary blood flow. The specific defects that will be present are: Aortopulmonary (AP) - Window Atrioventricular septal defect (AVSD) Double outlet right ventricle (DORV) Total anomalous pulmonary venous drainage (TAPVD) Truncus arteriosus Ventricular septal defect (VSD) Presence of postoperative PH immediately after intracardiac repair: Patients will be enrolled if mean PAP after intracardiac repair exceeds 25 mmHg after weaning from CPB. Exclusion Criteria: Specific cardiac defects: Atrial septal defect (ASD) Cyanotic congenital heart disease Univentricular atrio-ventricular - connexion Valvular or subvalvular pulmonary or aortic stenosis Specific circumstances: Emergency cardiac surgery Children presenting with infection after cardiac surgery Infants on extracorporeal membrane oxygenation (ECMO) before cardiac surgery Infants/children treated with epoprostenol Concomitant diseases: Systemic arterial hypertension Renal failure Diabetes mellitus Known bleeding disorders (known disorders of blood coagulation and hemostasis) Infection during the first 24 hours after cardiac surgery

Sites / Locations

  • University of Heidelberg, Medical Faculty, Department of Pediatric Cardiology

Outcomes

Primary Outcome Measures

Number of pulmonary hypertensive crises (major and/or minor)

Secondary Outcome Measures

Treatment with aerosolized ILO is equally effective as iNO in reducing the pulmonary artery pressure (PAP) within the first 72 hours after cardiopulmonary bypass surgery (CPB)
Patients treated with aerosolized ILO can be weaned earlier from mechanical ventilation than patients on iNO treatment
Patients treated with aerosolized ILO show the same in-hospital mortality as patients treated with iNO

Full Information

First Posted
October 6, 2005
Last Updated
December 11, 2012
Sponsor
Heidelberg University
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1. Study Identification

Unique Protocol Identification Number
NCT00235521
Brief Title
Iloprost-Study: Comparison of Nitric Oxide to Iloprost (Ventavis) for Treatment of Pulmonary Hypertension in Children After Cardiopulmonary Bypass Surgery
Official Title
Comparison of Inhaled Nitric Oxide With Aerosolized Iloprost (Ventavis®) for Treatment of Pulmonary Hypertension in Children After Cardiopulmonary Bypass Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
December 2012
Overall Recruitment Status
Completed
Study Start Date
May 2005 (undefined)
Primary Completion Date
October 2008 (Actual)
Study Completion Date
October 2008 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Heidelberg University

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Inhaled nitrous oxide (iNO) will be compared to aerosolized iloprost (ILO) in pediatric patients after cardiac surgery with pulmonary hypertension. The hypothesis is that iloprost is more effective in preventing pulmonary hypertensive crises.
Detailed Description
Investigators, Study Sites: Single-center trial at the Department of Pediatric Cardiology, Department of Cardiac Surgery and Department of Anesthesiology, University Medical Center, Heidelberg, Germany Exploratory proof of concept study (Investigator initiated trial) Indication: Postoperative pulmonary hypertension in infants and children undergoing cardiopulmonary bypass surgery for intracardiac repair of left-to-right shunt Objectives: To compare the efficacy of aerosolized iloprost with inhaled nitric oxide to prevent postoperative pulmonary hypertensive crises Design: Exploratory, open label, randomized study with parallel-group design; Duration of observation: 72 hours Population: Infants older than 4 weeks and children less than 18 months of age presenting with left-to-right shunt and increased pulmonary blood flow. Inclusion will be independent on the presence or absence of preoperative pulmonary hypertension Sample Size: 20 patients: inhaled nitric oxide (iNO) - group; 20 patients: aerosolized iloprost (ILO) -group Treatment: Both groups: controlled ventilation, sedation, analgetics, inotropic substances as required, standardized intensive care treatment. iNO - group: concentration of iNO at 10 ppm; administered by mechanical ventilation. ILO - group: aerosolized Iloprost at a dose of 0,5 µg/kg body weight (12x / 24h), administered by ultrasound nebulizer. Efficacy Parameters: Occurrence of "minor" or "major" pulmonary hypertensive crises (PHTC) Safety Parameters: Arterial blood pressure, oxygen saturation, complete blood count Statistical Procedures: All analyses in this exploratory trial are descriptive, giving confidence intervals for differences between treatment groups. Primary analysis variable: Rate of occurrence of "major" or "minor" pulmonary hypertensive crises Secondary variables: Presence of hours of pulmonary hypertension, Duration of mechanical ventilation

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pulmonary Hypertension
Keywords
Pulmonary hypertension, Cardiac Surgery, Children, Pediatric Patients, Iloprost, NO, nitric oxide, Pulmonary hypertension after cardiac surgery in pediatric patients, 0 - 2 years old

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
15 (Actual)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
aerosolized iloprost
Primary Outcome Measure Information:
Title
Number of pulmonary hypertensive crises (major and/or minor)
Secondary Outcome Measure Information:
Title
Treatment with aerosolized ILO is equally effective as iNO in reducing the pulmonary artery pressure (PAP) within the first 72 hours after cardiopulmonary bypass surgery (CPB)
Title
Patients treated with aerosolized ILO can be weaned earlier from mechanical ventilation than patients on iNO treatment
Title
Patients treated with aerosolized ILO show the same in-hospital mortality as patients treated with iNO

10. Eligibility

Sex
All
Maximum Age & Unit of Time
2 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent by parents or legal representatives Age: Infants older than 4 weeks of age and children less than 1½ years of age. Presence of a left-to-right shunt with increased pulmonary blood flow. The specific defects that will be present are: Aortopulmonary (AP) - Window Atrioventricular septal defect (AVSD) Double outlet right ventricle (DORV) Total anomalous pulmonary venous drainage (TAPVD) Truncus arteriosus Ventricular septal defect (VSD) Presence of postoperative PH immediately after intracardiac repair: Patients will be enrolled if mean PAP after intracardiac repair exceeds 25 mmHg after weaning from CPB. Exclusion Criteria: Specific cardiac defects: Atrial septal defect (ASD) Cyanotic congenital heart disease Univentricular atrio-ventricular - connexion Valvular or subvalvular pulmonary or aortic stenosis Specific circumstances: Emergency cardiac surgery Children presenting with infection after cardiac surgery Infants on extracorporeal membrane oxygenation (ECMO) before cardiac surgery Infants/children treated with epoprostenol Concomitant diseases: Systemic arterial hypertension Renal failure Diabetes mellitus Known bleeding disorders (known disorders of blood coagulation and hemostasis) Infection during the first 24 hours after cardiac surgery
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Matthias Gorenflo, MD, PhD
Organizational Affiliation
Heidelberg University
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Heidelberg, Medical Faculty, Department of Pediatric Cardiology
City
Heidelberg
ZIP/Postal Code
69120
Country
Germany

12. IPD Sharing Statement

Learn more about this trial

Iloprost-Study: Comparison of Nitric Oxide to Iloprost (Ventavis) for Treatment of Pulmonary Hypertension in Children After Cardiopulmonary Bypass Surgery

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