Endometrial Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are female and between 20 and 45 years old
- People with a body mass index (BMI) between 18.5 and 24.9 (a measure of body weight relative to height, considered a "normal" range)
- People who have previously been told by a doctor that they have uterine fibroids (non-cancerous growths in the uterus)
- People who are generally healthy and do not have any long-term health conditions that are uncontrolled
- People who report moderate to severe discomfort during their period, such as pelvic cramps, bloating, mood swings, or fatigue
- People who have been experiencing menstrual cramps for at least the past six months
- People who take hormonal birth control, provided they have been taking it consistently for at least three months and still have a regular period
- People who take over-the-counter supplements or herbal remedies, provided they have been taking them consistently for at least three months before the study starts and are willing to continue the same routine throughout the study
- People willing to avoid starting any new medications, supplements, or products for the entire duration of the study
- People willing to avoid any new supplements or herbal products aimed at affecting the menstrual cycle during the study
- People willing to avoid receiving any new vaccines for the six-month study period
- People who follow a regular, consistent exercise routine and are willing to keep that routine exactly the same throughout the study
- People willing to avoid lifestyle changes that could affect their menstrual cycle during the study (such as starting or stopping hormonal birth control or changing their exercise habits)
- People who use other therapies such as massage, chiropractic care, or acupuncture, and are willing to keep the frequency of those therapies the same throughout the study
- People who live in the United States
Who may not be able to join:
- People whose menstrual cycle is not regular (a regular cycle is defined here as 21–35 days)
- People who do not experience menstrual cramps
- People who follow an extreme dietary approach, such as dry fasting, water fasting, or a ketogenic diet
- People who have lost a significant amount of weight in the three months before the study starts
- People who are unwilling to stop taking any medications, herbal remedies, or supplements that could affect their menstrual cycle
- People with existing long-term health conditions — including cancer or psychiatric disorders — that would make it difficult to follow the study's requirements
- People with known severe allergic reactions
- People with any known allergies or sensitivities to the ingredients in the study product
- People who are pregnant, breastfeeding, trying to conceive, or who may become pregnant at any point during the study
- People who are unwilling to follow the study's rules and requirements
- People who have stopped, started, or changed their hormonal birth control in the past three months
- People who have previously used a product called Elix Cycle Balance
- People who currently smoke or have smoked in the past three months
- People who have been diagnosed with any of the following conditions: PCOS, endometriosis, PMDD, adenomyosis, Hashimoto's thyroiditis, Grave's disease or other thyroid disorders, hyperprolactinemia, Cushing's disease, congenital adrenal hyperplasia, or any eating disorder (including anorexia, bulimia, orthorexia, or binge eating disorder)
- People with a history of hormone-related conditions such as thyroid disorders or Type 1 or Type 2 diabetes
- People with a history of high blood pressure, high cholesterol, or a blood clot in a vein
- People with a BMI over 25 (considered overweight or obese)
- People with ongoing pelvic pain caused by other conditions, such as infections, gut-related conditions, psychological conditions, fibromyalgia, or chronic fatigue syndrome
- People who have had a hysterectomy, myomectomy, removal of both ovaries and fallopian tubes, or any other gynaecological medical or surgical treatment within the past six months
- People with a history of an abnormal pap smear result
- People with a history of gynaecological cancer or uterine abnormalities
- People with recurring urinary tract infections or diagnosed gut conditions such as IBS, IBD, Crohn's disease, or ulcerative colitis
- People who are currently taking part in another research study, or plan to do so at any point during the next 24 weeks
- People who consume more than five alcoholic drinks per week
- People who have received a vaccine within the past three months
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Phone: 4242450284
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Change in uterine fibroid-related symptom severity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.