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NCT06124313 · ClinicalTrials.gov registry record · NA

A Single Group Study to Evaluate the Effects of a Vaginal Probiotic on Vaginal and Digestive Health

A NA study, sponsored by Rael.

Completed
Registry status
NA
Development phase
40
Enrollment target

NCT06124313: Completed NA study, sponsored by Rael.

NCT06124313 is a NA study that has completed, run by Rael. The registered enrollment target is 40 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06124313, a NA study, has completed, sponsored by Rael.

COMPLETED
Registry status
NA
Development phase
40 participants
Enrollment target

Study Summary

This is a virtual single-group study that will last 12 weeks. Participants will take 1 capsule every day, with water. Questionnaires will be completed at baseline, 2 weeks, 4 weeks, and 12 weeks.

Primary Outcome

Participants will complete self-reported questionnaires reporting on incidence and severity of symptoms of bacterial vaginosis.

Interventions

  • DIETARY_SUPPLEMENT Vaginal Probiotic

Trial Details

FieldValue
Enrollment Target 40 participants
Start Date 2023-09-14
Est. Completion 2024-01-14
Phase NA
Rael

5 total trials

What the finished NCT06124313 record still lists

NCT06124313 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 40 participants, a relatively small participant target, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (97% lower).

The record links to 0 conditions, and to 1 intervention - of which Vaginal Probiotic is the first listed.

NCT06124313 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06124313 about?

NCT06124313 is a clinical study titled "A Single Group Study to Evaluate the Effects of a Vaginal Probiotic on Vaginal and Digestive Health". This is a virtual single-group study that will last 12 weeks. Participants will take 1 capsule every day, with water. Questionnaires will be completed at baseline, 2 weeks, 4 weeks, and 12 weeks.

What is the current status of trial NCT06124313?

This trial is currently completed. It is a NA study. The enrollment target is 40 participants. The study started on 2023-09-14. Estimated completion is 2024-01-14.

What interventions are being tested in trial NCT06124313?

The interventions under investigation include: Vaginal Probiotic (DIETARY_SUPPLEMENT).

Who is sponsoring clinical trial NCT06124313?

This trial is sponsored by Rael, which has 5 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06124313's enrollment target sits among peer trials

40 1447th of 2000 higher than 465 of 2,000 other NA trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06124313, the US trial registry maintained by the National Library of Medicine. NCT06124313 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.