An interventional study of Flora Power Probiotic Vaginal Suppository in Vaginal Health and Vaginal pH, sponsored by Love Wellness. Completed at 1 site in United States. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-08-21.
Sponsored by Love Wellness · Not applicable, Interventional, and Supportive care
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.
Love Wellness is the lead sponsor of 10 studies on the registry; none are open to participants now.
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Exclusion Criteria:
Participants will use the Flora Power suppository once daily at bedtime for 5 consecutive days when they feel they are experiencing any of the common signs of vaginal imbalance like vaginal malodor, vaginal irritation, and/or vaginal itching.
Dietary Supplement: Flora Power Probiotic Vaginal Suppository
The 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.
Effect on Vaginal pH and Health
Measure the change in vaginal pH levels with a test strip from baseline to 24 hours after the 5-day intervention period.
Time frame: Baseline, Day 6 (24 hours after the last suppository insertion)
Effect on Vaginal pH and Health
Measure the change in overall vaginal health from baseline to 24 hours after the 5-day intervention period with a questionnaire.
Time frame: Baseline, Day 6 (24 hours after the last suppository insertion)
Participant Perception of Vaginal Freshness and Odor
Evaluate participants' perceptions of the vaginal suppository's impact on vaginal freshness and odor, as well as the support of a calm, soothed, and balanced vaginal environment. This outcome measure is assessed with questionnaires.
Time frame: Baseline, Day 2, Day 5
Plan to share: No
No publications or documents are linked to this record.
Ran from May 2024 to primary completion in Jul 2024, 2 months.
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This study is completed, as verified in Aug 2024. You cannot join it, but the record below documents what was studied.
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