Real-world Aliskiren Use in Diabetic Patients
Completed
Conditions studied: Diabetes, Hypertension
In brief
The purpose of this study is to evaluate real-world patterns of aliskiren use with a focus of change in renal function following aliskiren initiation as well as to identify "triggering events" that lead to aliskiren initiation.
Key facts
- Study ID
- NCT01393860
- Run by
- Novartis
- People needed
- 200
- Starts
- 2010-12-01
- Last updated by the study team
- 2011-07-14
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Type 2 diabetes
- Patients ages 18 yeras and older
- Hypertension Diagnosis
- Currently on at least 1 hypertensive medication
- At least 2 lab measure before and after aliskiren initiation
You may not qualify if…
- Inadequate chart records where microalbuminuria, serum creatinine and blood pressure data are not within 3-12 months prior to initiation of Aliskiren
- Pregnancy
- Development of secondary renal disease unrelated to diabetes (such as nephritis)
- Terminal illness
- AIDS/HIV Other protocol-defined inclusion/exclusion criteria may apply
Where it is running
- MODEL Clinical Research, Research Division of Bay Endocrinology Associates GBMC Physicians pavilion North — Baltimore, Maryland, United States
Full record on ClinicalTrials.gov
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