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

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Matthias Gorenflo, University of Heidelberg
ClinicalTrials.gov Identifier:
NCT00235521
First received: October 6, 2005
Last updated: December 11, 2012
Last verified: December 2012

October 6, 2005
December 11, 2012
May 2005
October 2008   (final data collection date for primary outcome measure)
Number of pulmonary hypertensive crises (major and/or minor)
Same as current
Complete list of historical versions of study NCT00235521 on ClinicalTrials.gov Archive Site
  • 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
  • Treatment with aerosolized ILO is equally effective as iNO in reducing the pulmonary artery pressure (PAP) within the first 72 h after CPB.
  • Patients treated with aerosolized ILO can be weaned earlier from mechanical ventilation than patients on iNO reatment.
  • Patients treated with aerosolized ILO show the same in-hospital mortality as patients treated with iNO.
Not Provided
Not Provided
 
Iloprost-Study: Comparison of Nitric Oxide to Iloprost (Ventavis) for Treatment of Pulmonary Hypertension in Children After Cardiopulmonary Bypass Surgery
Comparison of Inhaled Nitric Oxide With Aerosolized Iloprost (Ventavis®) for Treatment of Pulmonary Hypertension in Children After Cardiopulmonary Bypass Surgery

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.

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

Interventional
Not Provided
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Pulmonary Hypertension
Drug: aerosolized iloprost
Not Provided
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
15
October 2008
October 2008   (final data collection date for primary outcome measure)

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
Both
up to 2 Years
No
Contact information is only displayed when the study is recruiting subjects
Germany
 
NCT00235521
Iloprost-Study
Yes
Matthias Gorenflo, University of Heidelberg
University of Heidelberg
Not Provided
Principal Investigator: Matthias Gorenflo, MD, PhD University of Heidelberg
University of Heidelberg
December 2012

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP