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

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-04-24

Study Completion Date

2024-06-24

Brief Summary

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This virtual single-group clinical trial aims to evaluate the effects of the Good Girl Probiotics supplement on vaginal health. Participants will take one capsule of the probiotic supplement daily for eight weeks. They will complete questionnaires at Baseline, after the first dose, and at the end of Weeks 2, 4, 6, and 8 to assess changes in vaginal pH, vaginal health, and urinary tract health.

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Detailed Description

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Conditions

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Vaginal Health Women's Health

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Probiotic Supplement Group

Participants in this group will receive the Good Girl Probiotics supplement.

Group Type EXPERIMENTAL

Good Girl Probiotics

Intervention Type DIETARY_SUPPLEMENT

Participants will take one capsule of the Good Girl Probiotics supplement daily in the morning for eight weeks.

Interventions

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Good Girl Probiotics

Participants will take one capsule of the Good Girl Probiotics supplement daily in the morning for eight weeks.

Intervention Type DIETARY_SUPPLEMENT

Eligibility Criteria

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Inclusion Criteria

* Female at birth.
* Aged 18+.
* Interested in supporting a balanced vaginal pH, vaginal health, and urinary tract health.
* Regularly experience symptoms of an unbalanced vagina, including an atypical smell, discharge, itching, swelling, irritation, pain during sex, and/or burning sensation while urinating.
* Willing to avoid using products or medications that target vaginal or urinary tract health infections.
* Willing to avoid other probiotics.
* Able to follow the study protocol.

Exclusion Criteria

* Two or more bladder infections in six months or three or more infections in a year.
* Recent surgeries or invasive treatments within the last six months.
* Use of products or medications targeting vaginal or urinary tract health in the last 12 weeks.
* Known allergies to the product ingredients.
* Chronic health conditions impacting participation.
* Pregnant, breastfeeding, or trying to conceive.
* History of substance abuse.
* Current or former smoker within the past six months.
* Participation in another clinical trial.
* Diagnosed vaginal or pelvic conditions.
* Use of vaginal-related birth control (NuvaRing, IUD).
* Changes in hormonal birth control in the last three months.

Minimum Eligible Age

18 Years

Eligible Sex

FEMALE

Accepts Healthy Volunteers

No