Can herbal supplements ease fibroid pain? new study seeks answers
NCT ID NCT07078682
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This 24-week study is testing two herbal supplements, Elix Cycle Balance and Elix Daily Harmony, in 42 women aged 20-45 with uterine fibroids. Participants take the supplements daily and report changes in symptoms like menstrual pain and bleeding through questionnaires. The goal is to see if these supplements can improve symptom severity and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Elix Cycle Balance and Elix Daily Harmony (herbal dietary supplements)
- What this could lead to
- If it works, this could point toward a natural supplement option to ease fibroid-related pain and improve quality of life.
- What could go wrong
- This is a small, early-stage study with no placebo group, so results may be biased or not generalizable. Supplements are not regulated like drugs, and effectiveness is uncertain.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
About 42 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Aug 2025
- Expected to finish
-
Jan 2026
An estimate. End dates often move.
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
20 to 45 years
- Sex
-
Female participants only
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Be female. * Be aged 20-45. * BMI 18.5 - 24.9 kg/m2 * Self-reported prior diagnosis of uterine fibroids. * Anyone who is generally healthy - does not live with any uncontrolled chronic disease. * Self-reported moderate to severe discomfort during menstruation, related to pelvic cramps, bloating, mood swings, or fatigue. * Self-reported menstrual cramps during their cycle, for the past six months minimum. * If taking hormonal birth control, has been doing so consistently for at least three months, and experiences a menstrual cycle with a period. * If taking other oral over-the-counter supplements or herbal remedies, has been consistently taking these for at least three months prior to starting the study, and is willing to maintain this routine for the study duration. * Willing to refrain from introducing any products or any new forms of medication or supplements for the study duration. * Willing to refrain from any other dietary supplements or herbal remedies targeting the menstrual cycle during the study period. * Willing to refrain from any new vaccines during the 6 month period. * Follows a stable, consistent exercise regimen and are willing, for the duration of the study, to not decrease or increase the amount of exercise in their regimen. * Agrees to refrain from any lifestyle changes that may affect their menstrual cycle for the duration of the study (for example, getting on or off hormonal birth control, reducing the amount of exercise). * If using any other interventions, such as massage, chiropractic medicine, or acupuncture, agrees not to increase or decrease the number of these other interventions during the study period. * Resides in the United States. Exclusion Criteria: * Does not experience a regular menstrual cycle (21-35 days). * Does not experience menstrual cramping. * Follows an extreme diet intervention such as dry fasts, water fasts, or ketogenic diets. * Anyone who has experienced significant weight loss in the past three months prior to study participation. * Unwilling to stop the use of any medication or herbal remedies/supplements that can affect the menstrual cycle. * Anyone with pre-existing chronic conditions that would prevent participants from adhering to the protocol, including oncological and psychiatric disorders. * Anyone with known severe allergic reactions. * Anyone with any allergies or sensitivities to any of the study product ingredients. * Any women who are pregnant, breastfeeding, or trying to conceive (or who will be at any point during the study period). * Anyone unwilling to follow the study protocol. * Has stopped, started, or changed hormonal birth control in the past three months. * Previous users of Elix Cycle Balance. * Anyone who is currently a smoker or has been a smoker in the past 3 months. * Anyone who has been diagnosed with the following conditions: PCOS, Endometriosis, PMDD, Adenomyosis, Hashimoto's thyroiditis, Grave's disease (and any other thyroid disorders), hyperprolactinemia, Cushing's disease, congenital adrenal hyperplasia, anorexia, bulimia, orthorexia, binge eating, any other eating disorder. * History of endocrine disorders such as thyroid disorder, Type 1 or 2 diabetes, or other. * History of hypertension, hyperlipidemia, or previous venous embolism. * Overweight/obesity (BMI \> 25 kg/m2). * Women with other causes of chronic pelvic pain, including infectious disease, gastrointestinal, psychological disorders, fibromyalgia, and chronic fatigue syndrome. * Hysterectomy, myomectomy, or bilateral salpingo-oophorectomy or other gynecological medical or surgical treatment in the last 6 months. * History of an abnormal pap smear. * History of neoplasia of gynecological origin and/or existence of uterine malformations. * Chronic urinary tract infections or diagnosed functional gastrointestinal conditions like IBS, IBD, Crohn's disease, or ulcerative colitis. * Currently partaking in another research study or will be partaking in any other research study for the next 24 weeks, or at any point during this study's duration. * Consume more than 5 alcoholic drinks per week * Had a vaccine in the last 3 months
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Leiomyoma are added.
Genom att skicka in godkänner du våra Användarvillkor
Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
Citruslabs
RECRUITINGLas Vegas, Nevada, 89118, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can big data improve safety in gynecologic surgery?
- Can a Double-Wall bag stop leaks during keyhole fibroid surgery?
- Can a single injection curb blood loss in fibroid surgery?
- Can watching videos before surgery calm nerves?
- A drug that may curb bleeding during fibroid surgery faces its first big test
- Could a common cholesterol drug shrink uterine fibroids?