The NaBu Effect on Menstruation in Women
Recruiting
N/A
Interventional Study
Menstrual Symptoms
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 15 (estimated)
- Sponsor
- Magdy Milad, MD · Other
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About This Trial
The purpose of this study is to evaluate the effect of once-daily Sodium butyrate (NaBu) on menstrual symptoms in women. The investigators posit that the use of NaBu will reduce menstrual symptoms after taking NaBu for 12 weeks.
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* 18 years or older.
* Menstruating regularly or irregularly
* Experiencing menstrual symptoms with an average baseline symptom score of at least 3 on a scale of 0 to 10 for at least one symptom during the initial pre-study rating period.
Exclusion Criteria:
* Pregnant or brea…
Contacts