Clinical Trials Directory

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

TypeNameDescription
DIETARY_SUPPLEMENTCombination of 2007RD01 and saw palmetto lipidic extractOral 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_SUPPLEMENTSaw palmetto lipidic extractOral 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.