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Sponsored by: |
Rigshospitalet, Denmark |
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Information provided by: | Rigshospitalet, Denmark |
ClinicalTrials.gov Identifier: | NCT00303004 |
The purpose of this study is to investigate if combination treatment with Bosentan and Sildenafil to patients with Eisenmenger syndrome is beneficial.
Condition | Intervention | Phase |
---|---|---|
Eisenmenger Syndrome |
Drug: Bosentan and Sildenafil |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Placebo Control, Crossover Assignment, Efficacy Study |
Official Title: | Combination Treatment With Bosentan and Sildenafil to Patients With Eisenmengers Syndrome |
Estimated Enrollment: | 20 |
Study Start Date: | March 2006 |
Study Completion Date: | January 2008 |
Primary Completion Date: | January 2008 (Final data collection date for primary outcome measure) |
Eisenmengers syndrome is condition with severe pulmonary arterial hypertension due to a shunting of blood from the left side of the heart to the right side of the heart. When the pressure in the pulmonary arteries levels the systemic blood pressure, blood begins to shunt from the right side of the heart to the left side of the heart leading to a condition with cyanosis, impaired physical capacity and increased mortality (Eisenmengers syndrome).
Several clinical trials have shown that there is a beneficial effect of treating patients with primary pulmonary arterial hypertension with Bosentan or Sildenafil and that a combination of these may have an additive or even synergistic effect. No clinical trials with Sildenafil and Bosentan has been conducted for patients with Eisenmengers syndrome. Observational studies and case stories indicate however that the effect of Bosentan or Sildenafil in patients with Eisenmengers syndrome may be as promising in these patients as in patients with primary pulmonary arterial hypertension.
We would like to examine the effect of treating patients with Eisenmengers Syndrome with a combination of Bosentan and Sildenafil.
The primary end point is change in physical performance measured with six minutes walking test.
Secondary end points is change in saturation, NYHA class, cardiac output (cardiac catheterization and innocor measurement), pulmonary vascular resistance (cardiac catheterization) shunt ratio (MRI), strain of right ventricle (BNP and echocardiography), quality of life and serum erythropoitin.
The trial is designed as a randomized, single centre, placebo controlled, double blind cross over study.
Twenty patients with Eisenmengers syndrome is included. All patients will be treated in three months with Bosentan. There after patients will be randomized to receive either Sildenafil (50 mg tid) or placebo as add on therapy for three month. Hereafter a cross over will be made and patients in combination treatment will receive only their native treatment and vice versa.
Examinations for primary and secondary endpoints will be made at baseline, before cross over and at the end of the study. All up titrating of medication will be performed during admittance. Patients will during the study period be close monitored with registration of adverse advents, physical examination and blood tests.
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Responsible Party: | Rigshospitaler ( Kasper Iversen ) |
Study ID Numbers: | 01000 |
Study First Received: | March 14, 2006 |
Last Updated: | January 23, 2008 |
ClinicalTrials.gov Identifier: | NCT00303004 |
Health Authority: | Denmark: Danish Medicines Agency; Denmark: The Danish National Committee on Biomedical Research Ethics |
Eisenmenger Complex Heart Diseases Cardiovascular Abnormalities Eisenmenger syndrome |
Sildenafil Congenital Abnormalities Heart Defects, Congenital Bosentan |
Vasodilator Agents Phosphodiesterase Inhibitors Pathologic Processes Disease Molecular Mechanisms of Pharmacological Action Therapeutic Uses |
Syndrome Enzyme Inhibitors Cardiovascular Diseases Cardiovascular Agents Antihypertensive Agents Pharmacologic Actions |