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Combination Treatment With Bosentan and Sildenafil to Patients With Eisenmengers Syndrome

Primary Purpose

Eisenmenger Syndrome

Status
Completed
Phase
Phase 3
Locations
Denmark
Study Type
Interventional
Intervention
Bosentan and Sildenafil
Sponsored by
Rigshospitalet, Denmark
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Eisenmenger Syndrome

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Eisenmenger syndrome Negative pregnancy test Exclusion Criteria: Elevated liver enzymes to more than 3´times normal value Hypotension (SBP < 90 mmhg). Mandatory treatment with nitrates Myocardial infarction within 3 months Stroke within 3 months Known allergy to Bosentan or Sildenafil inherited degenerative diseases in retina Breast feeding Suspicion of risc of noncompliance.

Sites / Locations

  • Rigshospitalet

Outcomes

Primary Outcome Measures

6 minutes walking distance

Secondary Outcome Measures

Pulmonary blood flow
Systemic blood flow
Pulmonary resistance
Shunt ratio
Erythropoitin
BNP
Saturation in rest
Saturation in activity
Quality of life
Right ventricle systolic and diastolic function
Working capacity
Oxygen consumption at rest
Oxygen consumption during maximal work

Full Information

First Posted
March 14, 2006
Last Updated
January 23, 2008
Sponsor
Rigshospitalet, Denmark
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1. Study Identification

Unique Protocol Identification Number
NCT00303004
Brief Title
Combination Treatment With Bosentan and Sildenafil to Patients With Eisenmengers Syndrome
Official Title
Combination Treatment With Bosentan and Sildenafil to Patients With Eisenmengers Syndrome
Study Type
Interventional

2. Study Status

Record Verification Date
January 2008
Overall Recruitment Status
Completed
Study Start Date
March 2006 (undefined)
Primary Completion Date
January 2008 (Actual)
Study Completion Date
January 2008 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Rigshospitalet, Denmark

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to investigate if combination treatment with Bosentan and Sildenafil to patients with Eisenmenger syndrome is beneficial.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Eisenmenger Syndrome

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
Double
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Drug
Intervention Name(s)
Bosentan and Sildenafil
Primary Outcome Measure Information:
Title
6 minutes walking distance
Secondary Outcome Measure Information:
Title
Pulmonary blood flow
Title
Systemic blood flow
Title
Pulmonary resistance
Title
Shunt ratio
Title
Erythropoitin
Title
BNP
Title
Saturation in rest
Title
Saturation in activity
Title
Quality of life
Title
Right ventricle systolic and diastolic function
Title
Working capacity
Title
Oxygen consumption at rest
Title
Oxygen consumption during maximal work

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Eisenmenger syndrome Negative pregnancy test Exclusion Criteria: Elevated liver enzymes to more than 3´times normal value Hypotension (SBP < 90 mmhg). Mandatory treatment with nitrates Myocardial infarction within 3 months Stroke within 3 months Known allergy to Bosentan or Sildenafil inherited degenerative diseases in retina Breast feeding Suspicion of risc of noncompliance.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Lars Soendergaard, MD
Organizational Affiliation
Rigshospitalet, Denmark
Official's Role
Principal Investigator
Facility Information:
Facility Name
Rigshospitalet
City
Copenhagen
ZIP/Postal Code
2100
Country
Denmark

12. IPD Sharing Statement

Citations:
PubMed Identifier
20202971
Citation
Iversen K, Jensen AS, Jensen TV, Vejlstrup NG, Sondergaard L. Combination therapy with bosentan and sildenafil in Eisenmenger syndrome: a randomized, placebo-controlled, double-blinded trial. Eur Heart J. 2010 May;31(9):1124-31. doi: 10.1093/eurheartj/ehq011. Epub 2010 Mar 3.
Results Reference
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Combination Treatment With Bosentan and Sildenafil to Patients With Eisenmengers Syndrome

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