Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:15 AM
Ignite Modification Date:
2025-12-25 @ 2:15 AM
NCT ID:
NCT05406960
Eligibility Criteria:
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
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
30 Years
Maximum Age:
55 Years
Study:
NCT05406960
Study Brief:
Protocol Section:
NCT05406960