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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT01042873
Other study ID # 0355-09-HMO-CTIL
Secondary ID 0355-09-HMO
Status Recruiting
Phase Phase 4
First received
Last updated
Start date January 2010
Est. completion date December 2021

Study information

Verified date March 2018
Source Hadassah Medical Organization
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2021
Est. primary completion date December 2020
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 40 Years
Eligibility Inclusion Criteria:

- healthy subjects

Exclusion Criteria:

- consumption of any medications during the 2 weeks prior to the study

- history of chest pain or tachycardia

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
3 hours intravenous dobutamine
Intravenous 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.

Locations

Country Name City State
Israel Hadassah University Hospital Jerusalem

Sponsors (1)

Lead Sponsor Collaborator
Hadassah Medical Organization

Country where clinical trial is conducted

Israel, 

References & Publications (1)

Bruck H, Leineweber K, Temme T, Weber M, Heusch G, Philipp T, Brodde OE. The Arg389Gly beta1-adrenoceptor polymorphism and catecholamine effects on plasma-renin activity. J Am Coll Cardiol. 2005 Dec 6;46(11):2111-5. Epub 2005 Nov 4. — View Citation

Outcome

Type Measure Description Time frame Safety issue
Primary Heart rate 3 hours
Secondary Systolic blood pressure 3 hours
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