Atenolol Exposure as Risk for Adverse Metabolic Responses to Beta Blockers
Completed · Not applicable
Conditions studied: Hypertension
In brief
The researchers hypothesize that the impact of increasing systemic exposure to atenolol leads to increased risk for adverse metabolic effects from atenolol therapy in hypertension. This will be accomplished through a 24-hour pharmacokinetic (PK) study and oral glucose tolerance test in hypertensive patients taking chronic atenolol 100 mg daily.
Key facts
- Study ID
- NCT00607347
- Run by
- University of Florida
- People needed
- 24
- Starts
- 2008-02-01
- Expected to finish
- 2009-06-01
- Last updated by the study team
- 2011-09-20
Who can join
Age: 18 and older, up to 65. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Subjects from PEAR who are on atenolol 100 mg once daily will be invited to participate
- Other inclusion criteria from PEAR
You may not qualify if…
- Patients with BMI >35 kg/m2 will be excluded
- Other exclusion criteria from PEAR
Where it is running
- University of Florida — Gainesville, Florida, United States
Full record on ClinicalTrials.gov
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