Clinical Trials Directory

Trials / Completed

CompletedNCT06565312

A Single Group Study to Evaluate the Effects of a Probiotic Vaginal Suppository on Vaginal Health.

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Love Wellness · Industry
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

This is a virtual single-group clinical trial lasting 8 weeks to evaluate the effects of a probiotic vaginal suppository on vaginal health. Participants will use the Flora Power suppository daily for 5 consecutive days when experiencing common signs of vaginal imbalance. They will complete questionnaires and vaginal pH tests before and after product use.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTFlora Power Probiotic Vaginal SuppositoryThe suppository contains Microcrystalline Cellulose, Ascorbic Acid, Vitamin C, Gelatin Capsule, Vaginal Probiotic Blend (Lactobacillus fermentum LF61, Lactobacillus acidophilus LA85, Lactobacillus plantarum Lp90), Magnesium Stearate, and Silicon Dioxide.

Timeline

Start date
2024-05-10
Primary completion
2024-07-10
Completion
2024-07-10
First posted
2024-08-21
Last updated
2024-08-21

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06565312. Inclusion in this directory is not an endorsement.

A Single Group Study to Evaluate the Effects of a Probiotic Vaginal Suppository on Vaginal Health. (NCT06565312) · Clinical Trials Directory