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

Love Wellness

Status: Completed

Conditions: Vaginal pH; Vaginal Health

Treatments: Dietary Supplement: Flora Power Probiotic Vaginal Suppository

Study type: Interventional

Funder types: Industry

Identifiers

NCT06565312

20434

Details and patient eligibility

About

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.

Enrollment: 40 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Female at birth, aged 18+.
• Interested in maintaining a healthy vaginal environment.
• Experience common signs of vaginal imbalance (e.g., malodor, irritation).
• Willing to avoid other vaginal products and follow study protocol.

Exclusion criteria

• Recent surgeries or invasive treatments.
• Use of vaginal health products in the last 12 weeks.
• Allergies to product ingredients.
• Chronic health conditions impacting participation.
• Pregnant, breastfeeding, or trying to conceive.
• History of substance abuse or smoking.
• Currently participating in another clinical trial.

Trial design

Primary purpose: Supportive Care

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

Flora Power Probiotic Vaginal Suppository

Experimental group

Description:

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.

Treatment:

Dietary Supplement: Flora Power Probiotic Vaginal Suppository