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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register.
Register: ClinicalTrials.gov
Last refreshed on: 19 February 2015
Main ID:  NCT00782782
Date of registration: 26/10/2008
Prospective Registration: No
Primary sponsor: Hadassah Medical Organization
Public title: Vascular Sensitivity to Adrenergic Agonists in Patients With CHF and in Healthy Subjects
Scientific title: Effect of Medications on Vascular Response in Patients With CHF and in Healthy Subjects
Date of first enrolment: August 2008
Target sample size: 80
Recruitment status: Active, not recruiting
URL:  http://clinicaltrials.gov/show/NCT00782782
Study type:  Observational
Study design:  Observational Model: Case Control, Time Perspective: Prospective  
Phase:  N/A
Countries of recruitment
Israel
Contacts
Name:     Mordechai Muszkat
Address: 
Telephone:
Email:
Affiliation:  Hadassah University Hospital
Key inclusion & exclusion criteria

Inclusion Criteria:

- Patients with congestive heart failure NYHA I-II

- Stable clinical condition

Exclusion Criteria:

- Resting systolic blood pressure < 100

- Resting heart rate < 50

- Hypersensitivity to dexmedetomidine, phenylephrine, isoproterenol, terbutaline



Age minimum: 18 Years
Age maximum: 70 Years
Gender: Both
Health Condition(s) or Problem(s) studied
Congestive Heart Failure
Intervention(s)
Primary Outcome(s)
vascular sensitivity (ED50) and response (Emax) to dexmedetomidine, phenylephrine, isoproterenol and terbutaline [Time Frame: 3 weeks]
Secondary Outcome(s)
Secondary ID(s)
366-28.12.07
Source(s) of Monetary Support
Please refer to primary and secondary sponsors
Secondary Sponsor(s)
Ethics review
Results
Results available:
Date Posted:
Date Completed:
URL:
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