Therapeutic Effect of Herbal Infusion on Menometrorrhagia (NCT05406960) | Clinical Trial Compass
CompletedNot Applicable
Therapeutic Effect of Herbal Infusion on Menometrorrhagia
Tunisia13 participantsStarted 2019-05-10
Plain-language summary
This is an interventional, non-randomized, controlled, pilot study that explores a new approach to treat, Abnormal uterine bleeding-menometrorrhagia in women, being candidates for hysterectomy, based on tea infusion consumption of a mixture of two plants.
Who can participate
Age range
30 Years – 55 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Inclusion Criteria:
* Women failed first-line intervention to stop bleeding and planned for hysterectomy
* Women between (30-50 years)
* Able to understand and provide informed consent to participate in the study.
* Not pregnant or lactating
* Having menstrual period more than 7 days with uterine bleeding at irregular intervals.
Exclusion Criteria:
Participants with at least one of the following criteria will not be included in the trial:
* Chronic disease with long-term treatment (i.e. asthma, cardiovascular disorders..)
* woman taking any standard medications for abnormal uterine bleeding
* Women who have a history of gastrointestinal bleeding or ulcer
* Women who have abnormal kidney function
* Participants with increasing menstrual bleeding during the treatment requires surgical emergency procedures.
* Those refusing the instructions or participating in other clinical trials.
* Participant take other herbal treatment
* \- Age less than 18 years
* \- Healthy Volunteers
* women with ovarian tumours
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.