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NCT04457401 · ClinicalTrials.gov registry record · NA
Probiotic and Gastrointestinal Symptoms Due to Menstruation in Healthy Women
A NA study, sponsored by University of Florida.
- Completed
- Registry status
- NA
- Development phase
- 187
- Enrollment target
NCT04457401 is a NA study that has completed, run by University of Florida. The registered enrollment target is 187 participants.
The verdict
NCT04457401, a NA study, has completed, sponsored by University of Florida.
- COMPLETED
- Registry status
- NA
- Development phase
- 187 participants
- Enrollment target
Study Summary
In this double blind, parallel study, female participants who are on an oral contraceptive will consume either a probiotic or placebo supplement for approximately 8 weeks. Menstrual cramp and abdominal pain severity, as measured by the visual analog scale, will be assessed daily. A subgroup of participants will be asked to provide vaginal swab and stool samples to assess microbial communities.
Interventions
- DIETARY_SUPPLEMENT Placebo
- DIETARY_SUPPLEMENT Probiotic
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 187 participants |
| Start Date | 2020-12-01 |
| Est. Completion | 2024-06-01 |
| Phase | NA |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT04457401
The ClinicalTrials.gov registry entry for NCT04457401 describes a study currently listed as completed, categorized as NA. The registered enrollment target is 187 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Florida, which has 1,106 total studies on file at ClinicalTrials.gov.
The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.
NCT04457401 reports 0 study locations.
Frequently Asked Questions
What is clinical trial NCT04457401 about?
NCT04457401 is a clinical study titled "Probiotic and Gastrointestinal Symptoms Due to Menstruation in Healthy Women". In this double blind, parallel study, female participants who are on an oral contraceptive will consume either a probiotic or placebo supplement for approximately 8 weeks. Menstrual cramp and abdominal pain severity, as measured by the visual analog scale, will be assessed daily. A subgroup of parti...
What is the current status of trial NCT04457401?
This trial is currently completed. It is a NA study. The enrollment target is 187 participants. The study started on 2020-12-01. Estimated completion is 2024-06-01.
What interventions are being tested in trial NCT04457401?
The interventions under investigation include: Placebo (DIETARY_SUPPLEMENT), Probiotic (DIETARY_SUPPLEMENT).
Who is sponsoring clinical trial NCT04457401?
This trial is sponsored by University of Florida, which has 1,106 total clinical trials registered on ClinicalTrials.gov.
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