Clinical Trials Directory

Trials / Completed

CompletedNCT01752543

Effects on Exercise Hemodynamics of Vasopressin Blockade by Conivaptan Infusion in Heart Failure Patients

Status
Completed
Phase
Phase 4
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Finn Gustafsson · Academic / Other
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Not accepted

Summary

The purpose of the present study is to evaluate the effects of a blockade of the vasopressin system and central hemodynamic system in heart failure (HF) patients during physical exercise. The significance of the vasopressin system during physical exercise is unclear. If vasopressin is a significant regulator of exercise hemodynamics in HF, strategies to intervene against activation of the V1A-receptor might be expected to improve HF symptoms and possibly outcome. The potential effects of the central hemodynamic system will be evaluated with a Swan-Ganz catheter. Echocardiography will be performed at rest and during submaximal working capacity before and during the infusion of a vasopressin receptor antagonist (conivaptan) or placebo. Cardiac output will be measured by thermodilution. The exercise test will be performed at 50 % of VO2 max and hemodynamic and echocardiographic measurements will be collected. The exercise test will be performed on a supine multistage bicycle.

Conditions

Interventions

TypeNameDescription
DRUGConivaptanConivaptan treatment: 20 mg bolus followed by infusion of 2 mg/hour
DRUGPlacebo (Dextrose)Placebo treatment: 20 mg bolus followed by infusion of 2 mg/hour

Timeline

Start date
2013-12-01
Primary completion
2015-06-01
Completion
2015-06-01
First posted
2012-12-19
Last updated
2015-06-17

Locations

1 site across 1 country: Denmark

Source: ClinicalTrials.gov record NCT01752543. Inclusion in this directory is not an endorsement.