Study of the Efficacy and Safety of Nebivolol in Younger Patients (18 - 54 Years)
Completed · Phase 4 · Has a placebo group
Conditions studied: Hypertension
In brief
The purpose of this study is to assess the efficacy, safety, and tolerability of 8 weeks of therapy with nebivolol in comparison to placebo in younger patients 18 - 54 years of age with stage 1 or stage 2 essential hypertension.
Key facts
- Study ID
- NCT01415531
- Run by
- Forest Laboratories
- People needed
- 641
- Starts
- 2011-08-01
- Expected to finish
- 2012-04-01
- Last updated by the study team
- 2013-05-16
Who can join
Age: 18 and older, up to 54. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Male and female outpatients, of age 18 - 54 years
- Patients diagnosed with stage 1 or stage 2 essential hypertension
- Normal physical examination findings and electrocardiogram (ECG) results or abnormal findings judged by the Investigator to be not clinically significant
You may not qualify if…
- Secondary hypertension or severe hypertension
- History of Type 1 diabetes mellitus
- A medical contraindication to discontinuing a current antihypertensive therapy
- Clinically significant respiratory disease that prohibit use of a beta blocker
Where it is running
- Forest Investigative Site 067 — Phoenix, Arizona, United States
- Forest Investigative Site 070 — Phoenix, Arizona, United States
- Forest Investigative Site 049 — Buena Park, California, United States
- Forest Investigative Site 034 — Burbank, California, United States
- Forest Investigative Site 039 — Costa Mesa, California, United States
- Forest Investigative Site 024 — Fountain Valley, California, United States
- Forest Investigative Site 020 — Fresno, California, United States
- Forest Investigative Site 021 — Fresno, California, United States
- Forest Investigative Site 040 — Greenbrae, California, United States
- Forest Investigative Site 047 — La Mesa, California, United States
- Forest Investigative Site 073 — Los Angeles, California, United States
- Forest Investigative Site 077 — Roseville, California, United States
- Forest Investigative Site 060 — San Bernardino, California, United States
- Forest Investigative Site 054 — San Francisco, California, United States
- Forest Investigative Site 018 — Spring Valley, California, United States
- Forest Investigative Site 028 — Denver, Colorado, United States
- Forest Investigative Site 059 — Brooksville, Florida, United States
- Forest Investigative Site 033 — Fort Lauderdale, Florida, United States
- Forest Investigative Site 006 — Hallandale, Florida, United States
- Forest Investigative Site 044 — Longwood, Florida, United States
- Forest Investigative Site 001 — Miami, Florida, United States
- Forest Investigative Site 012 — Miami, Florida, United States
- Forest Investigative Site 032 — Miami, Florida, United States
- Forest Investigative Site 055 — Miami, Florida, United States
- Forest Investigative Site 065 — Phoenix, Arizona, United States
Full record on ClinicalTrials.gov
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