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UnknownNCT01042873

The Hemodynamic Response to Prolonged Dobutamine Infusion

Status
Unknown
Phase
Phase 4
Study type
Interventional
Enrollment
100 (estimated)
Sponsor
Hadassah Medical Organization · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

A decrease in the response of beta 1 adrenergic receptors to agonists (desensitization) is thought to play a major role in the pathogenesis of diseases such as congestive heart failure. However, currently, there is no in vivo model that will enable us to measure desensitization of the hemodynamic responses to beta 1 adrenergic receptors in vivo. Our hypothesis is that constant 3 hours intravenous infusion of the selective beta1 adrenergic receptor agonist dobutamine will result in gradual decline in hemodynamic responses to dobutamine over time.

Conditions

Interventions

TypeNameDescription
DRUG3 hours intravenous dobutamineIntravenous dobutamine will be infused during 3 hours. At the first and last 0.5 hors of infusion dose will be increased gradually, while in the middle 2 hours dose will remain constant.

Timeline

Start date
2010-01-01
Primary completion
2020-12-01
Completion
2021-12-01
First posted
2010-01-06
Last updated
2018-06-12

Locations

1 site across 1 country: Israel

Source: ClinicalTrials.gov record NCT01042873. Inclusion in this directory is not an endorsement.