A Randomized Triple-Blind Placebo-Controlled Study to Evaluate the Effects of a Supplement on Lower Urinary Tract Symptoms in Men.
Completed · Not applicable · Has a placebo group
Conditions studied: Lower Urinary Tract Symptoms, Benign Prostatic Hyperplasia, Erectile Dysfunction
In brief
This study aims to evaluate the effects of the ProstaThrive™ supplement on lower urinary tract symptoms (LUTS) in men. It is a 90-day virtual, randomized, placebo-controlled trial with 80 male participants aged 40 and above. The primary endpoint is the reduction in LUTS, while secondary endpoints include changes in sexual function and performance.
Key facts
- Study ID
- NCT06504472
- Run by
- Optimale
- People needed
- 80
- Starts
- 2024-02-07
- Expected to finish
- 2024-06-24
- Last updated by the study team
- 2024-07-16
Who can join
Age: 40 and older. Sex: male. Healthy volunteers: not accepted.
You may qualify if…
- Male participants aged 40+
- Experience symptoms such as frequent nighttime urination, incomplete bladder emptying, weak urinary stream, and frequent daytime urination
- Difficulty in getting or maintaining an erection
- Willing to avoid introducing any new products or medications targeting LUTS or erectile dysfunction during the study period
You may not qualify if…
- Recent surgeries or invasive treatments
- History of prostate or male reproductive cancers
- Urinary issues caused by neurological conditions
- Previous surgery on the genitals, prostate, bladder, or urethra
- Known allergies to product ingredients
- Diagnosed with chronic health conditions impacting study participation
- Current substance abuse
- Participation in other clinical trials
- Taking medications or supplements targeting LUTS or erectile dysfunction
Where it is running
- Citruslabs — Santa Monica, California, United States
Full record on ClinicalTrials.gov
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