Pulmonary Valve Replacement in Large Right Ventricular Outflow Tract

This study has been completed.
Sponsor:
Collaborators:
Hôpital Necker-Enfants Malades
European Georges Pompidou Hospital
Information provided by:
Assistance Publique - Hôpitaux de Paris
ClinicalTrials.gov Identifier:
NCT00259207
First received: November 28, 2005
Last updated: September 29, 2009
Last verified: March 2007

November 28, 2005
September 29, 2009
December 2005
May 2009   (final data collection date for primary outcome measure)
Right ventricular function [ Time Frame: during the study ] [ Designated as safety issue: Yes ]
Right ventricular function
Complete list of historical versions of study NCT00259207 on ClinicalTrials.gov Archive Site
  • Morbidity and mortality [ Time Frame: during the study ] [ Designated as safety issue: Yes ]
  • Length of stay [ Time Frame: during the study ] [ Designated as safety issue: Yes ]
  • Morbidity and mortality
  • Length of stay
Not Provided
Not Provided
 
Pulmonary Valve Replacement in Large Right Ventricular Outflow Tract
Pulmonary Valve Replacement : Study of Comparison Between a Standard Surgical Approach With Extracorporeal Circulation and an Off-pump Hybrid Strategy.

The purpose of this study is to compare 2 techniques of pulmonary valve replacement in patients with a large right ventricular outflow tract: a standard surgical treatment using cardiopulmonary bypass versus a medico-surgical hybrid strategy without extracorporeal circulation.

Pulmonary regurgitation is a common complication late after complete correction of a tetralogy of Fallot. It progressively leads to a right ventricular dilatation that has been strongly associated with ventricular arrhythmia, sudden death and right ventricular insufficiency. Pulmonary valve replacement reduces the rate of complications but the precise timing for this procedure remains unknown. Moreover, pulmonary valve replacement, even before the occurrence of symptoms, doesn't allow for a total recovery in all patients. Reasons are not known, but cardiopulmonary bypass as well as late referral to surgery have been incriminated to explain the persistence of right ventricular dysfunction after surgical valvular. Therefore, a strategy avoiding cardiopulmonary bypass could potentially preserve the right ventricular function and in the meantime reduce the hospitalisation length and morbid-mortality. For the last six years, we and others have developed a technique of percutaneous pulmonary valve implantation. Encouraging results were reported in the treatment of failing right ventricular to pulmonary artery conduit, but presents indications are limited and the innovative technique could not be offered to most of patients requiring pulmonary valve replacement. In particular, to date, conventional surgery is the only approach for patients with large pulmonary trunk over 22 mm in diameter. We had the idea of collaborating with the surgeons to try to improve the outcome of valvular in these patients. We would like to investigate a hybrid strategy in those patients with large right ventricular outflow tract inaccessible to solely transcatheter technique. The studied technique will associate a surgical pulmonary artery banding without cardiopulmonary bypass immediately followed by a transventricular or a transvenous pulmonary valve insertion using a conventional valved stent. The purpose of this randomized study is to evaluate benefits and risks of the medico-surgical hybrid strategy, and to compare both strategies hybrid approach and conventional surgery with extracorporeal circulation in term of right ventricular function recovery.

Interventional
Phase 3
Allocation: Randomized
Endpoint Classification: Safety/Efficacy Study
Intervention Model: Parallel Assignment
Masking: Open Label
Primary Purpose: Treatment
Pulmonary Valve Insufficiency
  • Procedure: Pulmonary valve insertion
    Pulmonary valve insertion
    Other Name: Pulmonary valve insertion
  • Procedure: medical surgery hybride
    medical surgery hybride
    Other Name: medical surgery hybride
  • Active Comparator: classic surgery
    classic surgery
    Intervention: Procedure: Pulmonary valve insertion
  • Experimental: medical surgery hybride
    medical surgery hybride
    Intervention: Procedure: medical surgery hybride
Boudjemline Y, Schievano S, Bonnet C, Coats L, Agnoletti G, Khambadkone S, Bonnet D, Deanfield J, Sidi D, Bonhoeffer P. Off-pump replacement of the pulmonary valve in large right ventricular outflow tracts: a hybrid approach. J Thorac Cardiovasc Surg. 2005 Apr;129(4):831-7.

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
8
May 2009
May 2009   (final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Patient with surgical indication of pulmonary valve replacement for significant pulmonary regurgitation
  2. Pulmonary trunk diameter > 22mm
  3. Age > 5 years old or weight > 20kg
  4. Acceptance of protocol
  5. Social regimen security

Exclusion Criteria:

  1. No indication of pulmonary valve replacement
  2. Age < 5 years old or weight < 20kg
  3. Extra-cardiac disease with a vital prognosis under 6 months
  4. Heparin and contrast allergy
  5. Clinical or biological signs of infection
  6. Pregnancy
  7. Patients in emergency state
  8. Patients included in an another research protocol during the last months
Both
6 Years to 90 Years
No
Contact information is only displayed when the study is recruiting subjects
France
 
NCT00259207
P040413, AOR04068
Yes
Cecile Jourdain, Department Clinical Research of Developpement
Assistance Publique - Hôpitaux de Paris
  • Hôpital Necker-Enfants Malades
  • European Georges Pompidou Hospital
Principal Investigator: Younes BOUDJEMLINE, MD,PhD Assistance Publique - Hôpitaux de Paris
Assistance Publique - Hôpitaux de Paris
March 2007

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