Recruitment

Recruitment Status
Completed

Summary

Conditions
Pulmonary Embolism
Type
Interventional
Phase
Early Phase 1
Design
Allocation: RandomizedIntervention Model: Parallel AssignmentMasking: Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)Masking Description: Treatment was blinded by the institutional pharmacy embedding the placebo or treatment pill in a gelatinous capPrimary Purpose: Basic Science

Participation Requirements

Age
Between 80 years and 80 years
Gender
Both males and females

Description

Patients with PE randomized to a single oral dose of sildenafil 50mg (n=10) or placebo (n=10) as add-on to conventional therapy. Right ventricular function evaluated immediately before and shortly after (0.5-1.5h) randomization by right heart catheterization (RHC), trans-thoracic echocardiography (T...

Patients with PE randomized to a single oral dose of sildenafil 50mg (n=10) or placebo (n=10) as add-on to conventional therapy. Right ventricular function evaluated immediately before and shortly after (0.5-1.5h) randomization by right heart catheterization (RHC), trans-thoracic echocardiography (TTE), and cardiac magnetic resonance (CMR). The primary efficacy endpoint was cardiac index measured by CMR.

Tracking Information

NCT #
NCT04283240
Collaborators
Not Provided
Investigators
Principal Investigator: Asger Andersen, MD,PhD Aarhus University Hospital