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:
2025-12-24 @ 2:17 PM
Ignite Modification Date:
2025-12-24 @ 2:17 PM
NCT ID:
NCT04736095
Eligibility Criteria:
Inclusion Criteria:
* • Women between 20 and 60 years with abnormal uterine bleeding in form of heavy menstrual bleeding, irregular and heavy menstrual bleeding) diagnosed on non-enhanced two-dimensional ultrasonography with submucous fibroids.
* Absence of STD, PID, active vaginal bleeding.
Exclusion Criteria:
* Presence of general cause of abnormal uterine bleeding
* History of drug use that can cause vaginal bleeding (anticoagulants, OCPs, HRT)
* History of recent hormonal treatment
* High risk of undergoing hysteroscopy
* Vaginal, Vulval causes of bleeding
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
20 Years
Maximum Age:
60 Years
Study:
NCT04736095
Study Brief:
Protocol Section:
NCT04736095