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 @ 7:16 PM
Ignite Modification Date:
2025-12-24 @ 7:16 PM
NCT ID:
NCT05474703
Eligibility Criteria:
Inclusion Criteria:
* Sexually active patients with abnormal uterine bleeding
* Patients with no known malignancy history or suspected malignancy, patients with average smear results,
* Patients without bleeding diathesis,
* Patients using drugs that may cause vaginal bleeding,
Exclusion Criteria:
* Sexually inactive patients
* Patients in pregnancy or postpartum period,
* Patients with a known history of malignancy or suspected malignancy, patients with abnormal smear results,
* Patients with bleeding diathesis,
* Patients using drugs that may cause vaginal bleeding, patients with any organic pathology to explain the bleeding in gynecological examination
* Patients with a dislocated levonorgestrel-releasing intrauterine device
* Patients who have previously received different treatments for abnormal uterine bleeding
Healthy Volunteers:
True
Sex:
FEMALE
Minimum Age:
18 Years
Maximum Age:
45 Years
Study:
NCT05474703
Study Brief:
Protocol Section:
NCT05474703