A Study Comparing the Response of Patients With Hypertension to Amlodipine or Amlodipine Plus Benazepril.
Completed · Phase 3
Conditions studied: Hypertension
In brief
Comparison of the safety and efficacy of the combination of amlodipine/Benazepril to amlodipine monotherapy in patients with non-essential hypertension, not controlled on amlodipine alone.
Key facts
- Study ID
- NCT00171366
- Run by
- Novartis
- People needed
- 1422
- Starts
- 2004-07-01
- Expected to finish
- 2005-07-01
- Last updated by the study team
- 2016-04-06
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Outpatients 18 years of age or older.
- Male or female patients are eligible. Female patients must be either post-menopausal for one year or surgically sterile, or using effective, contraceptive methods such as barrier method with spermicide, or an intrauterine device.
- Patients with essential hypertension as measured by a validated device
You may not qualify if…
- Severe hypertension (DBP > 115 mmHg diastolic and/or SBP > 180 mmHg systolic).
- Other protocol-defined exclusion criteria may apply.
Where it is running
- Novartis Pharmaceuticals — East Hanover, New Jersey, United States
Full record on ClinicalTrials.gov
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