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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: EUCTR
Last refreshed on: 5 September 2016
Main ID:  EUCTR2015-000709-38-AT
Date of registration: 28/07/2015
Prospective Registration: Yes
Primary sponsor: Medical University of Graz
Public title: Effects of the drug Benzbromaron on the pulmonary vessels
Scientific title: Acute Effects of Benzbromaron on the pulmonary circulation
Date of first enrolment: 20/10/2015
Target sample size:
Recruitment status: Not Recruiting
URL:  https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2015-000709-38
Study type:  Interventional clinical trial of medicinal product
Study design:  Controlled: no Randomised: no Open: yes Single blind: no Double blind: no Parallel group: no Cross over: no Other: no If controlled, specify comparator, Other Medicinial Product: no Placebo: no Other: no Number of treatment arms in the trial: 1  
Phase:  Human pharmacology (Phase I): no Therapeutic exploratory (Phase II): yes Therapeutic confirmatory - (Phase III): no Therapeutic use (Phase IV): no
Countries of recruitment
Austria
Contacts
Name: Department for Pulmonology   
Address:  Auenbruggerplatz 20 8036 Graz Austria
Telephone: 4331638512183
Email: gabor.kovacs@klinikum-graz.at
Affiliation:  Medical University of Graz
Name: Department for Pulmonology   
Address:  Auenbruggerplatz 20 8036 Graz Austria
Telephone: 4331638512183
Email: gabor.kovacs@klinikum-graz.at
Affiliation:  Medical University of Graz
Key inclusion & exclusion criteria
Inclusion criteria:
informed consent
diagnosis of pulmonary arterial hypertension
age: 18-90 years
Medically indicated right heart catheterization
Are the trial subjects under 18? no
Number of subjects for this age range:
F.1.2 Adults (18-64 years) yes
F.1.2.1 Number of subjects for this age range 5
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range 5

Exclusion criteria:
known allergy against benzbromaron, gelborange S or another component of the drug or against a drug with similar chemical structure
decreased renal function (GFR<60ml/min/kg)
renal diathesis
severe lilver disease (Bilirubin >1.6 mg% or AST or ALT > 3x ULN)
known pregnancy
uncontrolled systemic arterial hypertension (at rest >150 mmHg systolic or 95 mmHg diastolic)
uncontrolled ventricular arrythmias
uncontrolled bradycard or tachycard supraventricular arrythmias
myicardial infarction in the last 12 months
acute pulmonary embolism in the last 6 months
ongoing iv or sc Prostanoidtherapy for pulmonary arterial hypertension


Age minimum:
Age maximum:
Gender:
Female: yes
Male: yes
Health Condition(s) or Problem(s) studied
Pulmonary arterial hypertension
MedDRA version: 18.1 Level: PT Classification code 10064911 Term: Pulmonary arterial hypertension System Organ Class: 10038738 - Respiratory, thoracic and mediastinal disorders
Therapeutic area: Diseases [C] - Cardiovascular Diseases [C14]
Intervention(s)

Trade Name: Benzbromaron AL
Product Name: Benzbromaron
Pharmaceutical Form: Film-coated tablet
INN or Proposed INN: BENZBROMARONE
CAS Number: 3562-84-3
Concentration unit: mg milligram(s)
Concentration type: equal
Concentration number: 100-

Primary Outcome(s)
Main Objective: to assess the change of pulmonary vascular resistance 2 hours after the application of 200mg benzbromaron
Primary end point(s): change in pulmonary vascular resistance
Secondary Objective: to assess the change of mean pulmonary arterial pressure, systemic blood pressure and oxygen saturation 2 hours after the application of 200mg benzbromaron
Timepoint(s) of evaluation of this end point: before the application of benzbromaron and two hours after benzbromaron
Secondary Outcome(s)
Secondary end point(s): mean pulmonary arterial pressure, systemic blood pressure and oxygen saturation
Timepoint(s) of evaluation of this end point: before the application of benzbromaron and two hours after benzbromaron
Secondary ID(s)
BBR
Source(s) of Monetary Support
Ludwig Boltzmann Institute for Lung Vascular Research
Medical University of Graz
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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