Trials / Completed
CompletedNCT00797394
Efficacy of Natural Extract 2007RD01 Combined With Saw Palmetto in Benign Prostatic Hyperplasia Patients Compared to Saw Palmetto
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 110 (estimated)
- Sponsor
- innoVactiv Inc. · Industry
- Sex
- Male
- Age
- 50 Years – 75 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine if the combination of 2007RD01, a natural extract, and saw palmetto lipidic extract, is more effective at treating lower urinary tract symptoms associated with benign prostatic hyperplasia than saw palmetto lipidic extract alone.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DIETARY_SUPPLEMENT | Combination of 2007RD01 and saw palmetto lipidic extract | Oral administration of one capsule containing a combination of 250 mg of 2007RD01 (a natural extract) and 160 mg of saw palmetto lipidic extract plus inactive fillers, twice a day between meals |
| DIETARY_SUPPLEMENT | Saw palmetto lipidic extract | Oral administration of one capsule of 160 mg of saw palmetto lipidic extract plus inactive fillers, twice a day between meals |
Timeline
- Start date
- 2008-11-01
- Primary completion
- 2010-07-01
- First posted
- 2008-11-25
- Last updated
- 2011-04-13
Locations
4 sites across 1 country: Canada
Source: ClinicalTrials.gov record NCT00797394. Inclusion in this directory is not an endorsement.