Safety of SonoVue on Pulmonary Hemodynamics
Status and phase
Conditions
Treatments
Details and patient eligibility
About
This is an intra-subject crossover comparative safety study to evaluate the effect of intravenous (IV) bolus injection of SonoVue on pulmonary hemodynamics.
Full description
Subjects will be divided into two groups based on their baseline mean pulmonary arterial pressure. Each subject will receive two injections in randomized order during right heart catheterization: one administration of SonoVue and one administration of placebo, either SonoVue followed by Placebo or Placebo followed by SonoVue. The purpose is to provide direct evidence on the presence or absence of pulmonary hemodynamic effect following IV administration of SonoVue versus any effects following IV administration of the same volume of placebo.
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
- Provides written informed consent male or female at least 18 years of age scheduled to undergo right heart catheterization for clinical reasons
Exclusion criteria
- Pregnant or lactating females
- Significant arrhythmia or non-sinus rhythm that may affect the ability to assess pulmonary hemodynamics by catheterization
- Known allergy to one of the ingredients in the investigational product or to any other contrast agents including ultrasound contrast agents
- Previously entered into the study or received an investigational compound within 30 days before admission into the study
- Unstable pulmonary and/or systemic hemodynamic condition that would affect the ability to evaluate the pharmacological or hemodynamic effect of the investigational products
Trial design
36 participants in 2 patient groups, including a placebo group
Trial contacts and locations
Loading...
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal