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 @ 10:03 PM
Ignite Modification Date:
2025-12-24 @ 10:03 PM
NCT ID:
NCT07083635
Eligibility Criteria:
Inclusion Criteria:
* Women aged 18 years and older
* Regular menstrual cycles : at least 1 cycle prior to contraceptive implant insertion
* Normal pelvic examination and transvaginal ultrasound results
* Normal cervical cancer screening within the past 3 years
* Irregular vaginal bleeding defined as: Bleeding for more than 8 consecutive days, or Bleeding-free intervals of 15 days or less
Exclusion Criteria:
* Previous treatment for irregular vaginal bleeding within the past 3 months
* Pregnancy
* Contraindications to estrogen or progestin use
* Allergy to estrogen or progestin
* Allergy to hormonal patches
* Heavy vaginal bleeding causing anemia symptoms such as: Fatigue/Fainting/Dizziness
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT07083635
Study Brief:
Protocol Section:
NCT07083635